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Review

Preparation, Antimicrobial Properties under Different Light Sources, Mechanisms and Applications of TiO2: A Review

by
Changyu Shang
,
Junyu Bu
and
Cui Song
*
Marine College, Shandong University, Weihai 264209, China
*
Author to whom correspondence should be addressed.
Materials 2022, 15(17), 5820; https://doi.org/10.3390/ma15175820
Submission received: 14 July 2022 / Revised: 5 August 2022 / Accepted: 6 August 2022 / Published: 24 August 2022
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Abstract

:
Traditional antimicrobial methods, such as antibiotics and disinfectants, may cause adverse effects, such as bacterial resistance and allergic reactions. Photocatalysts based on titanium dioxide (TiO2) have shown great potential in the field of antimicrobials because of their high efficiency, lack of pollution, and lack of side effects. This paper focuses on the antimicrobial activity of TiO2 under different light sources. To improve the photocatalytic efficiency of TiO2, we can reduce electron-hole recombination and extend the photocatalytic activity to the visible light region by doping with different ions or compounds and compounding with polymers. We can also improve the surface properties of materials, increase the contact area with microorganisms, and further enhance the resistance to microorganisms. In addition, we also reviewed their main synthesis methods, related mechanisms, and main application fields to provide new ideas for the enhancement of photocatalytic microorganism performance and application popularization in the future.

1. Introduction

Microbial pollution has become an important factor that threatens human health and can produce various toxins [1]. Pathogenic microorganisms can cause human diseases [2,3], and some microorganisms can cause food spoilage [4], molds in clothes [5], degraded water quality [6], and even biological corrosion of buildings [7], causing certain losses to human society.
To reduce the adverse effects of microorganisms, disinfectants, antibiotics, and other methods are used to kill microorganisms, but there are also many problems in using these methods. Disinfectants can produce disinfection byproducts (DBPs) with high toxicity [8,9], leading to asthma, allergic rhinitis, and other respiratory symptoms [10] and corrosion effects [11]. The excessive use of antibiotics will produce new drug-resistant strains. Drug-resistant strains will periodically explode, increasing the incidence and becoming a major challenge in the global public health field [12,13].
Among these antimicrobial strategies, photocatalytic antimicrobials can realize the efficient utilization of light energy with fewer side effects which has received a wide range of attention. The photocatalyst plays an important role in the photocatalytic antimicrobial process. Because of this reason, research on photocatalysts and photocatalytic antimicrobials has been increasing overall (Figure 1). Among many photocatalytic materials, TiO2 and its composites are the most widely studied photocatalysts due to their low cost, stability, and easy preparation. The photoelectrochemical properties of TiO2 have a history of nearly 100 years, and many breakthrough discoveries have also promoted its development. In 1938, Goodeve et al. [14] studied the photochemical bleaching of ‘Chlorazol Sky Blue’ with TiO2. In 1972, Fujishima and Honda discovered for the first time that TiO2 could be used as an electrode in the photocatalytic splitting of water [15]. Without any applied voltage, water could be decomposed into oxygen and hydrogen by visible radiation, thus realizing the transformation from optical energy to chemical energy. In 1997, Wang et al. [16] prepared TiO2-coated glass. After UV irradiation, the structure of the TiO2 coating showed highly amphiphilic characteristics, which made the TiO2-coated glass antifogged and self-cleaning.
In the field of photocatalytic antimicrobials, TiO2 and its composites have excellent killing effects on Escherichia coli, Staphylococcus aureus, Candida albicans, Aspergillus niger, and other microorganisms They can be widely used in sewage treatment, food packaging, self-cleaning fabrics, antimicrobial coatings, and other fields [17,18,19]. In this paper, the main preparation methods of TiO2, antimicrobial activity and improvement strategies under ultraviolet (UV) light and visible light, antimicrobial mechanisms, and applications are reviewed to provide ideas and directions for future research.

2. TiO2 and Its Composites Materials

2.1. Synthesis Methods

At present, there are many synthesis methods for TiO2 photocatalysts. The synthesis method and conditions have a great influence on the performance of the photocatalyst. Fully understanding the characteristics of photocatalyst synthesis methods is beneficial to improve not only the production efficiency but also the application.

2.1.1. Sol–Gel Method

The sol–gel method is one of the most commonly used methods for the synthesis of TiO2. This method does not require a high reaction temperature. It can control the texture and surface properties of the material by changing the pH value, temperature, and reaction time [20]. It has unique advantages in the composition and structure control of inorganic materials and hybrid materials [21,22], is the simplest, has a low cost, and is suitable for laboratory research [23]. The sol–gel method uses alcohol or water as the medium to prepare the final product through hydrolysis, polycondensation, aging, drying, and thermal decomposition [20,24] (Figure 2A). Vargas et al. [25] obtained ceramic powder by the sol–gel method and then controlled the subsequent heat treatment temperature to ensure the purity of the oxide and the nanometric size of the particles. The synthesized powders were amorphous up to a temperature T < 350 °C, with a particle size of 100 nm. Their SEM and TEM images are shown in Figure 2B. Tahmasebizad et al. [26] also used the sol–gel method to synthesize Cu and N-codoped TiO2 photocatalytic coating materials, which can be activated by visible light.

2.1.2. Microwave-Assisted Method

The microwave-assisted method is commonly used with other methods as a way to enhance photocatalytic performance. The microwave-assisted method can improve the dispersion of different phases, accelerate the reaction rate, and modify the components in the sample [27,28,29,30]. For example, Ates et al. [30] synthesized a target sample within 10 min under microwave irradiation (Figure 2C). Lu et al. [31,32] prepared two different metal-doped catalysts, TiO2-Ag (p = 600 W, T = 140 °C) and TiO2-Sm (p = 450 W, T = 170 °C), by a microwave hydrothermal method. The SEM images of the two catalysts are shown in Figure 2D. Experiments show that microwave irradiation can improve the photocatalytic activity of TiO2 by uniformly heating the reaction system from inside to outside and increasing the number of ·OH on the surface of TiO2-Ag/Sm.

2.1.3. Green Synthesis Method

In recent years, many studies have been conducted on green synthesis methods, which are based on natural raw materials and are environmentally friendly [33,34]. Green synthesis methods are often used in conjunction with other methods. The synthesis process shown in Figure 2E is a combination of the green synthesis method and coprecipitation method [35]. Sagadevan et al. [36] synthesized TiO2 nanoparticles using Myristica fragrans seed extract. The synthesized TiO2 can be activated by UV light and has antibacterial activity against Klebsiella pneumoniae and S. aureus.

2.1.4. Hydrothermal Method

The hydrothermal method is used to synthesize products with relatively small crystal structures, which is usually carried out in autoclaves with water as a medium at high temperature and high pressure [37]. Based on one-dimensional TiO2 obtained by calcining Ti foil at 800 °C, Sun et al. [38] prepared nanotube films by the hydrothermal method. The growth process of the nanotube structure from rutile TiO2 on Ti foil is investigated by the morphology change of TiO2 films prepared with different hydrothermal durations. TiO2 with different structures was prepared by a hydrothermal method using butyl titanate and absolute ethanol as raw materials [39]. Researchers found that anatase TiO2 is formed when the hydrothermal time is 12 h, TiO2 forms mixed crystals of anatase and rutile when the hydrothermal time is 24 h, and rutile TiO2 is formed when the hydrothermal time is 36 h. Their SEM images are shown in Figure 2F.

2.1.5. Atomic Layer Deposition and Magnetron Sputtering Methods

Atomic layer deposition (ALD) and magnetron sputtering (MS) methods are often used to prepare photocatalyst composite films. They can realize the doping [40] and deposition [41,42] of metal on photocatalysts or the loading of photocatalysts on other substrates [43,44], which can improve the optical properties of materials. The MS method is based on the principle of physical deposition, and the surface of the prepared film is flatter [45]. This method is also often influenced by the shape of the substrate, and film is deposited only on surfaces parallel to the target surface [46]. The composition and structure of the ALD method are highly controllable, and the thickness of the prepared film is uniform, which is not affected by the shape of the material. The reaction is generally divided into four steps: (1) Precursor supply, (2) Purge, (3) Reactant supply, (4) Purge (Figure 2G) [47]. The required thickness is obtained through multiple cycles. Abdulagatov et al. [44] made a V-doped TiO2 film on polypropylene (PP) hernia meshes by using the thermal ALD method after more than 100 cycles. The film thickness is 38 nm, having good photocatalytic antibacterial performance (Figure 2H).
Materials 15 05820 g002 550
Figure 2. (A) Steps involved in the sol–gel process to synthesize MONPs [20]; (B) scanning electron microscopy (SEM) (a) and transmission- electron microscopy (TEM) (b) images of antimicrobials synthesized by the sol–gel method and thermally treated at 350 °C for 2 h [25]; (C) illustration of rGO/TiO2 nanocomposite formation [30]; (D) SEM images of TiO2-Sm (a) and TiO2-Ag (b) [31,32]; (E) schematic diagram showing all steps involved in a generic green synthesis mediated by plant extract using the coprecipitation method [35]; (F) SEM images of different TiO2 samples [39]; (G) illustration of ALD [47]; (H) different PP mesh samples [44].
Figure 2. (A) Steps involved in the sol–gel process to synthesize MONPs [20]; (B) scanning electron microscopy (SEM) (a) and transmission- electron microscopy (TEM) (b) images of antimicrobials synthesized by the sol–gel method and thermally treated at 350 °C for 2 h [25]; (C) illustration of rGO/TiO2 nanocomposite formation [30]; (D) SEM images of TiO2-Sm (a) and TiO2-Ag (b) [31,32]; (E) schematic diagram showing all steps involved in a generic green synthesis mediated by plant extract using the coprecipitation method [35]; (F) SEM images of different TiO2 samples [39]; (G) illustration of ALD [47]; (H) different PP mesh samples [44].
Materials 15 05820 g002

2.2. Antimicrobial Activity under UV Light

UV irradiation is a common source of energy for TiO2 photocatalysts. TiO2 photocatalysts have a wide band gap energy of 3.2 eV and can be activated under UV light [17]. Table 1 lists some TiO2 antimicrobial materials that can be activated under UV light.
Heloisa N et al. [48] deposited three kinds of crystalline TiO2 films on commercially pure titanium (cp-Ti) by MS. As shown in Figure 3A, four groups of TiO2 films were obtained: (1) machined cp-Ti (control); (2) A-TiO2 (anatase); (3) M-TiO2 (mixture of anatase and rutile); and (4) R-TiO2 (rutile). Researchers collected volunteers’ oral saliva as a source of multispecies biofilms and observed the inhibition by different films (Figure 3B). The photocatalytic performance of the three kinds of crystalline TiO2 films increases with increasing UV irradiation time. Figure 3C shows the colony forming units (log10 CFU/cm2) of the total number on the surfaces after 1 h of UVA light exposure according to groups. The results showed that both A-TiO2 and M-TiO2 showed significant antibacterial activity after 1 h of UV irradiation (p < 0.001), and the number of bacteria decreased by approximately 99% and 99.9%, respectively, while the R-TiO2 film had no antibacterial effect on the multispecies biofilms (p < 0.05).
The photocatalytic properties of many materials are improved after modification. For example, Moongraksathum et al. [49] used the sol–gel method to prepare a series of TiO2 nanocomposite films with different silver contents (Ag/TiO2). Under UVA illumination for 1 h, the antibacterial effect of the film on E. coli can be higher than 99.99%, while that of TiO2 could only reach 16.33%. The killing effect on influenza A virus (H1N1) and enterovirus also reached nearly 100%. Silica is a kind of amorphous material with stable chemical properties. Chen et al. [50] synthesized a silica carrier by the gel method and then synthesized a composite material (TiO2@SiO2) by the hydrolysis method. SiO2 can increase the specific surface area and the ability of TiO2 to adsorb bacteria. The surface of normal E. coli was smooth, but the surface of TiO2@SiO2 treated E. coli became rough and even showed small holes, indicating that the cell membrane of E. coli was damaged (Figure 4A). As shown in Figure 4B,C, with increasing TiO2 component content, TiO2@SiO2 has excellent antibacterial properties under UVA light. Pessoa et al. [43] deposited TiO2 films on polyurethane (PU) and polydimethylsiloxane (PDMS) by the ADL method and studied the photocatalytic antibacterial effect on Candida albicans. Even in the absence of UV irradiation, TiO2/PU could inhibit the conversion of C. albicans to mycelium. Under UV irradiation, the CFU of TiO2/PDMS samples can be reduced to 80%, which is much higher than 25% in the control group.
Hayashi et al. [51] hydrothermally synthesized TiO2 nanosheets (NS) with highly oriented structures. By changing the ratio of F/Ti in the reaction raw material, a series of samples with different morphologies were obtained: For Streptococcus mutans, the sample with the best performance can make the bacterial survival rate less than 10% under UV irradiation, while that of the nonirradiated group was more than 40%. It maintained a bacterial survival rate below 40%, even at a low concentration (0.1 mg/L).
Table
Table 1. Antimicrobial effects of different TiO2 materials under UV light.
Table 1. Antimicrobial effects of different TiO2 materials under UV light.
MaterialGrain Size: nmMicroorganismLight SourceAntimicrobial ActivityReference
A-TiO2, M-TiO2, R-TiO2Approximately 300 nmStreptococcus sanguinis, Actinomyces naeslundii, and Fusobacterium nucleatumUVA 2 × 15 W (λ = 350 nm and intensity = 1.62 mW/cm2)Approximately 99.9% for M-TiO2 and 99% for A-TiO2, R-TiO2 had no antimicrobial activity[48]
Ag-TiO21–3 (Ag)E. coli, the influenza A virus (H1N1), and enterovirusUVA (20 W/cm2)>99.9% (1 wt% Ag/TiO2)[49]
TiO2(NS1.0, NS1.2, NS1.5, NS1.8, and NS2.0 with different F/Ti ratios)200–600 (length), 6–20 (thickness)S. mutans365 nm light (2.5 mW/cm2)Approximately 90% (NS1.0)[51]
Cu/TiO2 nonwoven fabric (NWF)20 (TiO2), 1–5 (Cu)HuNoV genogroup II genotype 4 (HuNoV GII.4)373-nm UVA-LED sourceThe optimum treatment conditions for inactivating the HuNoV GII.4 droplets were as follows: Cu:TiO2 ratio of 1:7.7 and the use of a 373 nm UVA-LED source for 48.08 min[52]
Polyurethane-acrylate-Ag/TiO2TiO2: 30(length), 3–4(diameter), Ag: 6(diameter)E. coli36 W mercury lamp (wavelength >245 nm)Approximately 97%[53]
Fe-TiO212–15E. coliBlack light blue lamp with the major fraction of irradiation occurring at 365 nmAlmost 100% (0.5% Fe-doped, 10 min)[54]
SiO2@ TiO220.49E. coliUVA (30 W)99.3%[50]

2.3. Antimicrobial Activity under Visible Light

UV light only accounts for 5% of sunlight, far less than 45% for visible light, while pure TiO2 can only be activated under a UV light source because of its shortfall response to visible light and the expeditious recombination rate of the photogenerated electron–hole pairs which greatly limits its utilization of solar energy [55]. If its absorption spectrum can move to the visible light region, full use of the readily available energy of sunlight can be made, and the photocatalytic efficiency can be improved [56]. Table 2 lists some different TiO2 antimicrobial materials that can be activated under visible light. Many methods have been adopted to improve the utilization rate of light energy and strengthen the antimicrobial effect of materials [57].

2.3.1. TiO2-Metal Composites

TiO2Ag [58], Pt [59], Cu [58,60], Fe [61], Cr [62], V [44], and other metals can improve the photocatalytic antimicrobial activity of TiO2 by forming composites through modification, doping, and surface deposition.
Gomez-Polo et al. [62] found that the antibacterial ability of Cr-doped TiO2 under visible light can reach more than 200 times that under dark conditions. Cr promotes the shift of the absorption spectrum from UV to visible light, and the distribution is uniform in TiO2, which increases the efficiency of receiving optical energy. Au and Pt NPs can be used as intermediate carriers for the valence electron transition to the conduction band of TiO2, extending the photocatalytic activity to the visible region [59,63,64], which improves the photocatalytic antibacterial efficiency of materials. The V-doped TiO2 photocatalytic coating prepared by the ACL method can effectively inhibit the adhesion of S. aureus and E. coli. Doping V makes TiO2 produce a more intense redox reaction under visible light, killing microorganisms more effectively and preventing the formation of biofilms [44]. Figure 5A shows the antibacterial properties of TiO2 doped with different metals against E. coli in the dark (a) and under light (b). The antibacterial properties of some materials, such as Ag-TiO2 and Cu-TiO2, have better performance under visible light than in the dark [58]. Moon et al. [59] deposited Au and Pt coatings on TiO2 nanotubes (Figure 5B). These coatings have different bacterial adhesion abilities, and the colony-forming unit (CFU) values of the control group were lower than those of the light-free condition under visible light irradiation, especially under visible light irradiation at 470 nm wavelength. Figure 5C shows the results of the agar diffusion test of S. aureus (a) and CFUs of S. aureus under visible light irradiation at 470 nm and 600 nm (b).

2.3.2. Nonmetal Doping

In addition to the metals mentioned above, TiO2 is often doped with nonmetals such as N, F [65], B [66], and C [67] to improve its photocatalytic antimicrobial properties by modifying the band structure of TiO2 [45,68].
Mukherjee et al. [65] prepared N, F-doped TiO2 particles with sizes of 175–225 nm. The absorption wavelength is extended to the visible light region (Figure 6A(a,b)) These particles can stably produce ·OH (Figure 6A(c,d)) and inhibit spore germination in a dose-dependent manner, especially under visible light. (Figure 6B). Figure 6C shows images of fungal colonies after 5 days/18 days of treatment with different doses of nanoparticles in the presence/absence of visible light. The nanoparticles had obvious inhibitory effects on fungi at 5 days and 18 days under light conditions.
Boron and its derivatives also enable TiO2 to exhibit photocatalytic antibacterial activity [66,69,70]. The B-p and O-2p orbitals can be mixed to reduce the band gap, reduce electron-hole recombination, and effectively improve the photocatalytic activity [71]. Wong et al. [66] prepared a series of B-doped TiO2 thin films (117–484 nm; TiO2(B)), of which a 484 nm film (484-nm TiO2(B)) has the best photocatalytic antibacterial properties (Figure 7A(a–h)). Compared with the dark treatment conditions, the 484-nm TiO2(B) film under visible light irradiation had similar killing effects on gram-positive bacteria (S. aureus and Streptococcus pyogenes) and gram-negative bacteria (Acinetobacter baumannii and E. coli) (Figure 7B). Under visible light irradiation, a certain amount of carbon-doped TiO2 inactivated Bacillus subtilis within half an hour, and the killing rates of vegetative cells and spores of B. cereus, Bacillus thuringiensis, and Bacillus anthracis were higher than those under dark conditions (Figure 7C,D). It can also reduce the toxicity of anthrax lethal toxins by inactivating toxin protein components. Surviving cells under a subbacterial dose of photocatalyst are also more likely to be eliminated by phagocytes [67]. In addition, graphene or carbon nanotubes (CNTs) can also be used as a matrix to composite with TiO2, which can also improve the catalytic efficiency [72,73]. Figure 7E [69] shows the antibacterial effect of different samples on E. coli. The addition of B and CNTs enhances the photocatalytic antibacterial ability of TiO2, and the 3B-TiO2-CNT sample has the best photocatalytic antibacterial effect (Figure 7F).

2.3.3. Polymer Doping, Oxides and Others

In addition to the two strategies of metal doping and nonmetal doping, the strategies of oxide and polymer composites are also often used to enhance the photocatalytic antimicrobial performance of TiO2 [74,75,76,77].
Polymers often play a role in improving the dispersion of photocatalysts. For example, a polyacrylate shell can make the particle surface have zwitterionic charge, which makes it have good dispersion in aqueous solution. Particles in solution can form colloids and effectively contact the fungal cell membrane [65]. A uniform distribution of TiO2 in organic conjugated polymers (CPs) is conducive to the formation of large interfacial regions, which can maximize the utilization of photocatalysts at the minimum cost and reduce the subsequent separation process. In addition, CPs can also resist UV radiation; have excellent electron mobility; improve the overall conductivity, corrosion resistance, and environmental stability of materials; and optimize the organic–inorganic interactions [78]. After TiO2 was combined with high-performance microporous polymers (CMP/TiO2), its killing effect on E. coli and S. aureus reached 98.14% and nearly 100%, respectively (Figure 8A). CMP can increase the optical absorption of TiO2 to produce more ·OH and ·O2- to destroy the cell membrane, which induces the content to leak out and leads to cell death (Figure 8B,C) [75]. Chitosan can be combined with TiO2 nanoparticles through its amino and hydroxyl groups to form composite materials with degradation properties, and the absorption spectrum also moves in the visible light direction [79]. Polyaniline has a strong absorption capacity for visible light. TiO2 nanoparticles can also be fixed on the surface of polyaniline-coated kapok fibers (PANI-KpF), and the killing ability toward E. coli under light can be increased by 30% [80].
Compared with other semiconductor metal oxides, TiO2 has the advantages of photochemical stability and nontoxicity and is often used as the main photocatalyst compound with other oxides [81,82]. Ag2O [83], ZnO [84], and other oxides can form heterostructures with semiconductors such as TiO2. Liu et al. [85] found that the TiO2/Ag2O heterostructure can kill almost all E. coli after 60 min of visible light irradiation, showing strong photocatalytic bactericidal activity (Figure 9A(a,b)). FeOX [86], Cu2O [87], and other materials can also be combined with TiO2 to achieve antibacterial effects by generating free radicals. Yao et al. [88] synthesized SnSO4-modified TiO2. Figure 9B shows the antibacterial activity of pure TiO2 and different contents of SnSO4-TiO2 against E. coli (a–g) and S. aureus (A–G). For 5 mol% SnSO4/TiO2, the activity against E. coli was 93.6% and that against S. aureus was 85%. SnSO4/TiO2 has better antibacterial activity under light than in the dark (Figure 9C).
Materials 15 05820 g009 550
Figure 9. (A) Photocatalytic antibacterial efficiency toward E. coli with photocatalysts under visible light (a) and antibacterial effect of TiO2/Ag2O (1: 4) on E. coli under visible light (b) [85]; (B) antibacterial activity of different samples against E. coli (1–7) and S. aureus (8–14); (C) antibacterial activity of different samples against E. coli (c) and antibacterial activity of pure TiO2 and xSnSO4-TiO2 against S. aureus in the presence/absence of visible light (d) [88].
Figure 9. (A) Photocatalytic antibacterial efficiency toward E. coli with photocatalysts under visible light (a) and antibacterial effect of TiO2/Ag2O (1: 4) on E. coli under visible light (b) [85]; (B) antibacterial activity of different samples against E. coli (1–7) and S. aureus (8–14); (C) antibacterial activity of different samples against E. coli (c) and antibacterial activity of pure TiO2 and xSnSO4-TiO2 against S. aureus in the presence/absence of visible light (d) [88].
Materials 15 05820 g009
Table
Table 2. Antimicrobial effect of different TiO2 materials under visible light.
Table 2. Antimicrobial effect of different TiO2 materials under visible light.
MaterialGrain Size: nmMicroorganismLight SourceAntimicrobial EffectReference
Au/Pt-TiO2Au (1 min of coating): 9.36 ± 1.88 (diameter),
8.77 ± 1.90 (height)
Pt (2 min of coating): 20.72 ± 5.21 (diameter),
30.42 ± 6.01 (height)		S. aureusVisible light (470 nm)Au TiO2 NTs: colony forming unit decreased from approximately 235 to 60 (×104 CFU/mL)
Pt TiO2 NTs: colony forming unit decreased from approximately 290 to 75 (×104 CFU/mL)		[59]
Ag and Au/TiO2Ag:6
Au:14		E. coliVisible light (>420 nm)Ag TiO2 NTs: almost 100% after 1 h
Au TiO2 NTs: increased 4 times compared to that under UV irradiation (77.5%)		[89]
Cr-TiO25.8E. coliVisible light (360–740 nm)>95% (100μg/mL)[62]
Cu, Pt and Ag-TiO212–15 (catalyst)E. coliVisible light (>450 nm)>99%[58]
Fe-TiO219.24–22.24E. coliVisible light (400–700 nm)97.57% (0.1 at% of Fe-doped TiO2 films)[61]
TiO2(B)117–484 (thickness)E. coli, A. baumannii, S. aureus and S. pyogenesVisible light (60 W, incandescent lamp)Approximately 50%[66]
B-TiO2-CNT12–18E. coliVisible light (>400 nm)Almost 100% (3B-TiO2-CNT nanocomposites)[69]
B/Ce-TiO223E. coli and S. aureusVisible lightAlmost 99% (S. aureus)
Almost 100% (E. coli)		[71]
Ag2O-TiO25–30E. coliVisible light (>400 nm)Almost 100%[83]
Cu2O/TiO28E. coli and C. albicansVisible light (>420 nm)>99%[87]
CuO/TiO223.6–24.2(anatase), 42.8–44.5(rutile)S. aureusVisible lightAlmost 100%[90]
Polyaniline-kapok fiber/TiO26.06E. coliVisible light30% less than that in the dark[91]
Au/ZnO-TiO210 (Au), 50 (ZnO)E. coli-98.2%[92]
CMP/TiO2650–950E. coli and S. aureusVisible light (LED)98.14% (E. coli), nearly100% (S. aureus)[75]

3. Antimicrobial Mechanism

ROS produced by the material play a major role in the antimicrobial process. The antimicrobial effect of photocatalysts often starts from the broken cell membrane. Then, the antimicrobial effect of photocatalysis can be achieved in many ways; for example, the lipid layer on the cell surface is destroyed, resulting in the leakage and destruction of intracellular substances such as proteins and DNA [93,94,95,96], the destruction of the intracellular electron transport system, and the inactivation of intracellular enzymes [97,98]. Particularly, among many types of TiO2-based photocatalysts, TiO2-metal composites can release additional metal ions. ROS and metal ions jointly play a role in the antimicrobial process. ROS can attack the structure of cells, while metal ions can contact cells through electrostatic adsorption and other functions, causing denaturation of proteins and other substances [99,100]. ROS are produced by the material itself at the beginning. After the release of metal ions, ROS can also be generated by metal ions. In the following sections, we will discuss the production of ROS and the damage of ROS and metal ions on the cell membrane.

3.1. Production and Function of Reactive Oxygen Species

Photocatalysts can produce a variety of ROS, which can cause peroxidation of the cell membrane, produce lipid peroxide, change the fluidity and permeability of the cell membrane, cause cell content to flow out, and cause cell death [101,102,103,104]. ROS may be the most important contributors to antimicrobial activity [105].

3.1.1. Production of ROS

The energy band of a photocatalyst is composed of a valence band (VB) and conduction band (CB), and there is a band gap energy between them. Under the excitation of a certain light energy, the electrons excited in the VB transition to the CB, while leaving holes in the VB, forming electron-hole pairs. Electrons and oxygen molecules generate ·O2−, and holes and water molecules can generate ·OH, which play a major role in photocatalytic antimicrobial activity. Redox reactions occur on the surface of semiconductors due to the creation of positive holes and negative electrons [106,107,108].
However, electron-hole recombination reduces the efficiency of the carrier, and TiO2 can only be activated under UV light, so researchers can improve the photocatalytic efficiency by modifying the materials. For example, SiO2/TiO2 materials show good adsorption to bacteria and a large specific surface area and can produce · O2−, ·OH, and H2O2 to kill cells [50] (Figure 10A). The Fermi level of Ag below the conduction band of TiO2 can modify TiO2. Doped silver exists on the surface of TiO2 and does not affect the crystal structure of TiO2 particles. The photogenerated electrons transfer to silver on the surface of TiO2, and a Schottky barrier is formed at the Ag/TiO2 interface, which hinders the recombination of electron-hole pairs [109,110], promotes interface charge transfer (IFCT) and electron-hole separation efficiency, and improves the capture efficiency of O2 [83,111] (Figure 10B).

3.1.2. Function of ROS

Many studies have clearly shown that TiO2 nanoparticles can produce various ROS in aqueous solution, such as ·OH and O2- and H2O2 [65,88,112,113]. ·OH and H2O2 can damage DNA and cellular proteins. The ·OH produced by N and Fdoped TiO2 nanoparticles synthesized by Mukherjee et al. [65] can react with the glucan and chitin layers of fungal cell walls, resulting in cell wall degradation and subsequent cell death (Figure 11A). Yao et al. [88] synthesized SnSO4-modified TiO2, which can first oxidize enzymes and proteins related to the biofilm. After entering the cells, ROS can continue to attack the cells and eventually cause cell death (Figure 11B). The silver ions loaded on the photocatalyst can attack the mitochondrial membrane and cause mitochondrial damage, which can produce more ROS killing cells after damage [114,115].

3.2. Release and Function of Metal Ions

The release of metal ions also plays an important role in the antimicrobial process. First, metal ions have high affinity for negatively charged cell membrane surfaces, and they can also produce ROS, which kill the microbial cell membrane and lead to cell membrane dysfunction [98,116]. After the microbial cell membrane is attacked, it breaks, which exposes the organelles inside the cell. Ti4+ in TiO2 has little contribution to the antimicrobial activity [117], but TiO2-loaded Ag [58], Au [89], Cu [58], and Zn [84] can lose electrons to form metal ions, dissolving in the solution. The toxicity of metal ions to cells is related to the morphology of the catalysts and microbial types [49,75,118,119]. For example, Ag has a certain affinity for N and S and can react with proteins and nucleic acids containing thiol and amino groups [120,121,122]. The following figures are schematic diagrams of the effect of metal ions (Figure 12A) and TiO2 (Figure 12B) particles on cells, which have certain similarities.
The homeostasis of metal ions is critical to microbial life because they are involved in the regulation of various alternative functions, such as dehydrogenases, cofactors and catalysts, and structural stabilizers of enzymes and DNA-binding proteins [124]. Therefore, some bacteria have developed mechanisms that regulate the inhalation and outflow of metal ions to maintain stable intracellular ion concentrations [125]. However, excess metals or metal ions are toxic to bacterial cells. Metal can be adsorbed on the cell membrane, which destroys the charge balance of the cell membrane and leads to cell deformation [100,126]. For example, in enzyme and protein solutions, ZnO plays a fatal role in the production of ionic signals between various cells and intercellular cytoplasmic instruments [127]. Zeta-positive ZnO nanoparticles can destroy the membrane of gram-negative E. coli [128]. Due to their oxidizing ability, zinc ions react not only with organic functional groups (thioglycosides, carboxyl groups, and hydroxyl groups) but also with bacterial cells and membrane proteins. They enter bacterial cells and disrupt their electron transport system, resisting enzyme and protein gene expression functions and thus producing targeted antibacterial effects [97].

4. Applications

TiO2 and its modified composites show excellent photocatalytic antimicrobial activity after light irradiation. They have broad application prospects in food packaging and preservation [129], self-cleaning fabric [130,131], and so on [129,132].

4.1. Food Packaging and Preservation

Microbial contamination is a potential risk factor for food safety and quality, which may lead to outbreaks of foodborne diseases [133]. Heat treatment is a common sterilization method in food, but it may also lead to adverse changes, such as loss of nutrients. Currently, the application of nonthermal treatment in food has attracted increasing attention [134,135,136]. TiO2 can be used for food packaging to prevent microbial contamination.
Goudarzi et al. [137] prepared an eco-friendly starch-TiO2 composite that can absorb UV light, reducing the damage of singlet oxygen generated by UV radiation to food vitamins and proteins and the oxidation of lipids. TiO2 can also be prepared into composite films with k-carrageenan (KC) and konjac glucomannan (KGM). The killing effect of this film on Penicillium viridicatum reached nearly 80% after 6 h of illumination, which can be applied to the preservation and storage of strawberry [138] (Figure 13A,B). TiO2 can also be used in combination with chitosan to prepare composite films [116]. The film killed more than 90% of four typical foodborne pathogens, E. coli (gram-negative bacteria), S. aureus (gram-positive bacteria), C. albicans (fungi), and A. niger (molds), after 4 h of visible light irradiation, especially 99.9% of E. coli. After 12 h of treatment, all tested strains were completely killed. This film showed effective resistance to bacteria and fungi, which could be applied to the preservation of grapes, and the preservation period could reach 15 days (Figure 13C). TiO2 can be used to control tomato Fusarium wilt. As shown in Figure 13D, tomatoes were infected with fungal spores in the marked areas followed by visible-light treatment for 8 days. Tomato soaked in N, F-doped TiO2 particles at the wound will not be infected by Fusarium oxysporum after 8 days [65].

4.2. Self-Cleaning Fabric

In our daily clothing, we inevitably encounter various microorganisms. Cotton fabric has strong moisture absorption and good air permeability, which is conducive to the reproduction of microorganisms [139]. This damages the fabric, and at the same time, the close contact between the fabric and the human body poses a threat to human health [140,141]. Luckily, these bacteria have poor resistance because the environment is suitable for their growth, and self-cleaning clothing can play a better role [142].
Zhu et al. [143] prepared a new antibacterial material ZIF-L@TiO2/fabric by mixing TiO2 with zeolitic imidazolate framework-L (ZIF-L) and applied it to fabrics. ZIF-L and TiO2 can synergistically produce more ROS. As shown in Figure 14A, the LB liquid culture medium treated with ZIF-L@TiO2/fabric under irradiation conditions became clearer than that of the other groups. ZIF-L@TiO2/fabric can reduce the bacterial viability of E. coli to 2% under light, demonstrating a strong antibacterial ability. The ZIF-L@TiO2/fabric was placed on LB solid medium and cultured for 5 days, and the antibacterial effect was still obvious (Figure 14B). N, F-doped TiO2 can also be applied to cotton fabric surfaces to make light-responsive self-cleaning clothing; N, F-doped TiO2 also exhibits excellent surface hydrophobicity, which makes it difficult for water droplets to lubricate its surface [144] (Figure 14C), and Cu-doped TiO2 can also effectively remove coffee stains [145] (Figure 14D).

4.3. Others

In addition to their application in food packaging and fabric, photocatalytic antimicrobial materials have many applications in other fields. For example, in the field of building materials, TiO2 can be used as a semitransparent antibacterial coating. Under UV light irradiation, it showed significant antibacterial activity and resistance to biofilm formation [146,147] (Figure 15A). Figure 15A is a 24 h fluorescence map of the experiment, in which red represents bacteria and image (c-1) was taken at the center of the sample (c-1) and image (c-2) at the edge. It can be seen that the amount of bacteria with the coating is significantly reduced, while more bacteria exist in the part without the coating. In the field of sewage treatment, photocatalytic antimicrobials can also be used as disinfectants for sewage to inhibit microbial production [148,149,150,151]. Under illumination at 25 °C, the sample can exert a certain bactericidal effect on different types in sewage treatment at 25 ℃ [148] (Figure 15B). In the field of medicine, photocatalysts can be used for oral biofilm inhibition [48]. TiO2 can also be used in osteogenic materials, which have excellent properties such as antibacterial, osteogenic, and wear resistance [152] (Figure 15C). Under UV irradiation, Ti6Al4V/TiO2/SrTiO3 had the largest bacteriostatic zone (Figure 15D), and the proliferation rate of E. coli cultured on Ti6Al4V/TiO2/SrTiO3 was only 3%, while as a control, the proliferation rate of Ti6Al4V reached 36%. The antibacterial properties of the material can reduce the risk of bacterial infection during surgery.

5. Conclusions

TiO2 shows enormous potential in the field of photocatalytic antimicrobials. In this paper, the antimicrobial activities of TiO2 photocatalysts under different light sources, especially under visible light, were reviewed based on the source of energy–optical energy. In addition, we also reviewed their main synthesis methods, antimicrobial mechanisms, and application fields. We can reduce the electron-hole recombination, improve the surface properties, and increase the contact area with bacteria by doping metal ions, nonmetal ions and compounding with polymers to extend the photocatalytic activity to the visible light region and enhance the photocatalytic performance. These materials can inhibit microbial activity and achieve antimicrobial effects by producing ROS and hydroxyl free radicals to destroy the integrity of the cell membrane, damage microbial DNA, and inhibit enzyme activity.
However, the photocatalytic antimicrobial mechanism still needs to be further studied. We still need to study the photocatalytic kinetics more systematically, clarify the various effects of modified materials on photocatalytic antimicrobial properties, and connect the photocatalytic properties and antimicrobial properties of the materials more closely so that the materials can be widely used in food packaging, self-cleaning fabrics, sewage treatment, and other fields. The preparation of photocatalysts has a great influence on their photocatalytic antimicrobial performance. The preparation method should be selected depending on the application field, which requires us to have a further understanding of the preparation method and conditions. For nonmetal-doped photocatalysts, although this kind of photocatalyst can modify the band structure of TiO2, the nonmetallic elements contained in it can be removed at high temperature, making it difficult to control the content of nonmetallic elements. This puts forward a very high requirement on the preparation conditions. In addition, although TiO2-metal composites have an additional ion release effect and polymers can also change the surface properties of particles, their durability, such as polymer aging, should also be considered. It is believed that with the deepening of research, catalysts with high photocatalytic and antimicrobial properties, such as TiO2, will be more widely used.

Author Contributions

C.S. (Changyu Shang): writing―original draft, writing―review and editing, and software. J.B.: writing―original draft and data curation. C.S. (Cui Song): validation, methodology, and supervision. All authors have read and agreed to the published version of the manuscript.

Funding

The authors acknowledge support from the National Natural Science Foundation of China (4217030124), Natural Science Foundation of Shandong Province (ZR2021MB052, ZR2020MB140), and Shandong University-Weihai Research Institute of Industry Technology Research Projects (0004202107020002).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare that they have no known competing financial interest or personal relationship that could have appeared to influence the work reported in this paper.

References

  1. Eichelberger, K.R.; Cassat, J.E. Metabolic Adaptations During Staphylococcus aureus and Candida albicans Co-Infection. Front. Immunol. 2021, 12, 797550. [Google Scholar] [CrossRef] [PubMed]
  2. Liu, C.M.; Shen, Y.; Yang, M.; Chi, K.M.; Guo, N. Hazard of Staphylococcal Enterotoxins in Food and Promising Strategies for Natural Products against Virulence. J. Agric. Food Chem. 2022, 70, 2450–2465. [Google Scholar] [CrossRef] [PubMed]
  3. Kotloff, K.L. Bacterial diarrhoea. Curr. Opin. Pediatr. 2022, 34, 147–155. [Google Scholar] [CrossRef] [PubMed]
  4. Jafarzadeh, S.; Hadidi, M.; Forough, M.; Nafchi, A.M.; Khaneghah, A.M. The control of fungi and mycotoxins by food active packaging: A review. Crit. Rev. Food Sci. Nutr. 2022, in press. [Google Scholar] [CrossRef]
  5. Gulati, R.; Sharma, S.; Sharma, R.K. Antimicrobial textile: Recent developments and functional perspective. Polym. Bull. 2022, 79, 5747–5771. [Google Scholar] [CrossRef]
  6. Sayinli, B.; Dong, Y.J.; Park, Y.; Bhatnagar, A.; Sillanpaa, M. Recent progress and challenges facing ballast water treatment-A review. Chemosphere 2022, 291, 132776. [Google Scholar] [CrossRef]
  7. Stanaszek-Tomal, E. Environmental Factors Causing the Development of Microorganisms on the Surfaces of National Cultural Monuments Made of Mineral Building Materials-Review. Coatings 2020, 10, 1203. [Google Scholar] [CrossRef]
  8. Li, C.; Lin, Q.F.; Dong, F.L.; Li, Y.H.; Luo, F.; Zhang, K.J. Formation of iodinated trihalomethanes during chlorination of amino acid in waters. Chemosphere 2019, 217, 355–363. [Google Scholar] [CrossRef]
  9. Mustapha, S.; Jimoh, T.; Ndamitso, M.; Abdulkareem, S.A.; Taye, S.D.; Mohammed, A.K.; Amigun, A.T. The Occurrence of N-nitrosodimethylamine (NDMA) in Swimming Pools: An Overview. Environ. Health Insights 2021, 15, 117863022110365. [Google Scholar] [CrossRef]
  10. Rosenman, K.D.; Reilly, M.J.; Wang, L. Calls to a State Poison Center Concerning Cleaners and Disinfectants From the Onset of the COVID-19 Pandemic through April 2020. Public Health Rep. 2021, 136, 27–31. [Google Scholar] [CrossRef]
  11. Bonin, L.; Vitry, V.; Olivier, M.G.; Bertolucci-Coelho, L. COVID-19: Effect of disinfection on corrosion of surfaces. Corros. Eng. Sci. Technol. 2020, 55, 693–695. [Google Scholar] [CrossRef]
  12. Chomcheon, S.; Lenbury, Y.; Sarika, W. Stability, Hopf bifurcation and effects of impulsive antibiotic treatments in a model of drug resistance with conversion delay. Adv. Differ. Equ. 2019, 2019, 274. [Google Scholar] [CrossRef]
  13. Mohanty, H.; Pachpute, S.; Yadav, R.P. Mechanism of drug resistance in bacteria: Efflux pump modulation for designing of new antibiotic enhancers. Folia Microbiol. 2021, 66, 727–739. [Google Scholar] [CrossRef]
  14. Goodeve, C.F.; Kitchener, J.A. Photosensitisation by titanium dioxide. Trans. Faraday Soc. 1938, 34, 570–579. [Google Scholar] [CrossRef]
  15. Fujishima, A.; Honda, K. Electrochemical photolysis of water at a semiconductor electrode. Nature 1972, 238, 37–38. [Google Scholar] [CrossRef]
  16. Wang, R.; Hashimoto, K.; Fujishima, A.; Chikuni, M.; Kojima, E.; Kitamura, A.; Shimohigoshi, M.; Watanabe, T. Light-induced amphiphilic surfaces. Nature 1997, 388, 431–432. [Google Scholar] [CrossRef]
  17. Yadav, H.M.; Kim, J.-S.; Pawar, S.H. Developments in photocatalytic antibacterial activity of nano TiO2: A review. Korean J. Chem. Eng. 2016, 33, 1989–1998. [Google Scholar] [CrossRef]
  18. Muruganandham, M.; Zhang, Y.F.; Suri, R.; Lee, G.J.; Chen, P.K.; Hsieh, S.H.; Sillanpaa, M.; Wu, J.J. Environmental Applications of ZnO Materials. J. Nanosci. Nanotechnol. 2015, 15, 6900–6913. [Google Scholar] [CrossRef]
  19. Verbic, A.; Gorjanc, M.; Simoncic, B. Zinc Oxide for Functional Textile Coatings: Recent Advances. Coatings 2019, 9, 550. [Google Scholar] [CrossRef]
  20. Parashar, M.; Shukla, V.K.; Singh, R. Metal oxides nanoparticles via sol-gel method: A review on synthesis, characterization and applications. J. Mater. Sci. Mater. Electron. 2020, 31, 3729–3749. [Google Scholar] [CrossRef]
  21. Faustini, M.; Grosso, D.; Boissiere, C.; Backov, R.; Sanchez, C. “Integrative sol-gel chemistry”: A nanofoundry for materials science. J. Sol-Gel Sci. Technol. 2014, 70, 216–226. [Google Scholar] [CrossRef]
  22. Faustini, M. Sol-gel engineering to tune structural colours. J. Sol-Gel Sci. Technol. 2020, 95, 504–516. [Google Scholar] [CrossRef]
  23. Pant, B.; Park, M.; Park, S.-J. Recent Advances in TiO2 Films Prepared by Sol-Gel Methods for Photocatalytic Degradation of Organic Pollutants and Antibacterial Activities. Coatings 2019, 9, 613. [Google Scholar] [CrossRef]
  24. Gupta, S.M.; Tripathi, M. A review on the synthesis of TiO2 nanoparticles by solution route. Cent. Eur. J. Chem. 2012, 10, 279–294. [Google Scholar] [CrossRef]
  25. Vargas, M.A.; Rodriguez-Paez, J.E. Amorphous TiO2 nanoparticles: Synthesis and antibacterial capacity. J. Non-Cryst. Solids 2017, 459, 192–205. [Google Scholar] [CrossRef]
  26. Tahmasebizad, N.; Hamedani, M.T.; Shaban Ghazani, M.; Pazhuhanfar, Y. Photocatalytic activity and antibacterial behavior of TiO2 coatings co-doped with copper and nitrogen via sol-gel method. J. Sol-Gel Sci. Technol. 2020, 93, 570–578. [Google Scholar] [CrossRef]
  27. Karthik, K.; Vijayalakshmi, S.; Phuruangrat, A.; Revathi, V.; Verma, U. Multifunctional Applications of Microwave-Assisted Biogenic TiO2 Nanoparticles. J. Clust. Sci. 2019, 30, 965–972. [Google Scholar] [CrossRef]
  28. Stanciu, I.; Predoana, L.; Cusu, J.P.; Preda, S.; Anastasescu, M.; Vojisavljevic, K.; Malic, B.; Zaharescu, M. Thermal behaviour of the TiO2-based gels obtained by microwave-assisted sol-gel method. J. Therm. Anal. Calorim. 2017, 130, 639–651. [Google Scholar] [CrossRef]
  29. Liu, W.; Ge, M.; Zhu, Y.; Gao, Q. Photocatalytic Dye Degradation by TiO2 Nanocups Synthesized via Microwave-Assisted Solvothermal Method. Nanosci. Nanotechnol. Lett. 2017, 9, 1579–1583. [Google Scholar] [CrossRef]
  30. Ates, M.; Bayrak, Y.; Yoruk, O.; Caliskan, S. Reduced graphene oxide/Titanium oxide nanocomposite synthesis via microwave-assisted method and supercapacitor behaviors. J. Alloys Compd. 2017, 728, 541–551. [Google Scholar] [CrossRef]
  31. Lu, Y.J.; Wang, X.; Bi, X.J. Study on the preparation of Ag doped TiO2 catalyst by microwave hydrothermal method and its photocatalytic activity. In Proceedings of the 7th International Conference on Education, Management, Computer and Society (EMCS), Shenyang, China, 17–19 March 2017; pp. 839–845. [Google Scholar]
  32. Lu, Y.J.; Wang, X.; Bi, X.J. Study on the Preparation of Sm Doped TiO2 Catalyst by Microwave Hydrothermal Method and its Photocatalytic Activity. In Proceedings of the 7th International Conference on Education, Management, Computer and Society (EMCS), Shenyang, China, 17–19 March 2017; pp. 110–117. [Google Scholar]
  33. Irshad, M.A.; Nawaz, R.; Rehman, M.Z.U.; Adrees, M.; Rizwan, M.; Ali, S.; Ahmad, S.; Tasleem, S. Synthesis, characterization and advanced sustainable applications of titanium dioxide nanoparticles: A review. Ecotoxicol. Environ. Saf. 2021, 212, 111978. [Google Scholar] [CrossRef] [PubMed]
  34. Nabi, G.; Qurat ul, A.; Khalid, N.R.; Tahir, M.B.; Rafique, M.; Rizwan, M.; Hussain, S.; Iqbal, T.; Majid, A. A Review on Novel Eco-Friendly Green Approach to Synthesis TiO2 Nanoparticles Using Different Extracts. J. Inorg. Organomet. Polym. Mater. 2018, 28, 1552–1564. [Google Scholar] [CrossRef]
  35. Goncalves, R.A.; Toledo, R.P.; Joshi, N.; Berengue, O.M. Green Synthesis and Applications of ZnO and TiO2 Nanostructures. Molecules 2021, 26, 2236. [Google Scholar] [CrossRef]
  36. Sagadevan, S.; Lett, J.A.; Vennila, S.; Prasath, P.V.; Kaliaraj, G.S.; Fatimah, I.; Leonard, E.; Mohammad, F.; Al-Lohedan, H.A.; Alshahateet, S.F.; et al. Photocatalytic activity and antibacterial efficacy of titanium dioxide nanoparticles mediated by Myristica fragrans seed extract. Chem. Phys. Lett. 2021, 771, 138527. [Google Scholar] [CrossRef]
  37. Marfur, N.A.; Jaafar, N.F.; Khairuddean, M.; Nordin, N. A Review on Recent Progression of Modifications on Titania Morphology and its Photocatalytic Performance. Acta Chim. Slov. 2020, 67, 361–374. [Google Scholar] [CrossRef] [PubMed]
  38. Sun, Y.; Qian, J.; Zhao, Q.R.; Yang, S.S.; Yang, Y.; Zhao, Q. Hydrothermal synthesis of rutile TiO2 nanotubes film on Ti foil for photocatalytic degradation. Dig. J. Nanomater. Biostruct. 2021, 16, 579–584. [Google Scholar]
  39. Tang, M.; Xia, Y.; Yang, D.; Liu, J.; Zhu, X.; Tang, R. Effects of Hydrothermal Time on Structure and Photocatalytic Property of Titanium Dioxide for Degradation of Rhodamine B and Tetracycline Hydrochloride. Materials 2021, 14, 5674. [Google Scholar] [CrossRef]
  40. Chiappim, W.; Testoni, G.; Miranda, F.; Fraga, M.; Furlan, H.; Saravia, D.A.; Sobrinho, A.D.; Petraconi, G.; Maciel, H.; Pessoa, R. Effect of Plasma-Enhanced Atomic Layer Deposition on Oxygen Overabundance and Its Influence on the Morphological, Optical, Structural, and Mechanical Properties of Al-Doped TiO2 Coating. Micromachines 2021, 12, 588. [Google Scholar] [CrossRef]
  41. Al-Maliki, F.J.; Al-Rubaiy, M.A. Synthesis and study the concentration effect on the photocatalytic activity of titania nanoparticles as anti-bactria using reactive magnetron sputtering technique. Opt. Quantum Electron. 2022, 54, 1–11. [Google Scholar] [CrossRef]
  42. Lou, B.S.; Chen, W.T.; Diyatmika, W.; Lu, J.H.; Chang, C.T.; Chen, P.W.; Lee, J.W. High power impulse magnetron sputtering (HiPIMS) for the fabrication of antimicrobial and transparent TiO2 thin films. Curr. Opin. Chem. Eng. 2022, 36, 100782. [Google Scholar] [CrossRef]
  43. Pessoa, R.S.; dos Santos, V.P.; Cardoso, S.B.; Doria, A.; Figueira, F.R.; Rodrigues, B.V.M.; Testoni, G.E.; Fraga, M.A.; Marciano, F.R.; Lobo, A.O.; et al. TiO2 coatings via atomic layer deposition on polyurethane and polydimethylsiloxane substrates: Properties and effects on C. albicans growth and inactivation process. Appl. Surf. Sci. 2017, 422, 73–84. [Google Scholar] [CrossRef]
  44. Abdulagatov, I.M.; Ragimov, R.M.; Khamidov, M.A.; Maksumova, A.M.; Abdullaeva, N.M. ALD coated polypropylene hernia meshes for prevention of mesh-related post-surgery complications: An experimental study in animals. Biomed. Mater. 2022, 17, 015006. [Google Scholar] [CrossRef]
  45. Qi, L.; Guo, B.H.; Lu, Q.; Gong, H.H.; Wang, M.; He, J.L.; Jia, B.; Ren, J.; Zheng, S.C.; Lu, Y.F. Preparation and Photocatalytic and Antibacterial Activities of Micro/Nanostructured TiO2-Based Photocatalysts for Application in Orthopedic Implants. Front. Mater. 2022, 9, 914905. [Google Scholar] [CrossRef]
  46. Smietana, M.; Drazewski, T.; Firek, P.; Mikulic, P.; Bock, W.J. Comparison of Al2O3 nano-overlays deposited with Magnetron Sputtering and Atomic Layer Deposition on optical fibers for sensing purposes. In Proceedings of the Conference on Micro/Nano Materials, Devices, and Systems, Melbourne, Australia, 9–11 December 2013. [Google Scholar]
  47. Sibanda, D.; Oyinbo, S.T.; Jen, T.C. A review of atomic layer deposition modelling and simulation methodologies: Density functional theory and molecular dynamics. Nanotechnol. Rev. 2022, 11, 1332–1363. [Google Scholar] [CrossRef]
  48. Pantaroto, H.N.; Ricomini-Filho, A.P.; Bertolini, M.M.; Dias da Silva, J.H.; Azevedo Neto, N.F.; Sukotjo, C.; Rangel, E.C.; Barao, V.A.R. Antibacterial photocatalytic activity of different crystalline TiO2 phases in oral multispecies biofilm. Dent. Mater. 2018, 34, E182–E195. [Google Scholar] [CrossRef]
  49. Moongraksathum, B.; Chien, M.-Y.; Chen, Y.-W. Antiviral and Antibacterial Effects of Silver-Doped TiO2 Prepared by the Peroxo Sol-Gel Method. J. Nanosci. Nanotechnol. 2019, 19, 7356–7362. [Google Scholar] [CrossRef]
  50. Chen, Y.; Tang, X.; Gao, X.; Zhang, B.; Luo, Y.; Yao, X. Antimicrobial property and photocatalytic antibacterial mechanism of the TiO2-doped SiO2 hybrid materials under ultraviolet-light irradiation and visible-light irradiation. Ceram. Int. 2019, 45, 15505–15513. [Google Scholar] [CrossRef]
  51. Hayashi, K.; Nozaki, K.; Tan, Z.; Fujita, K.; Nemoto, R.; Yamashita, K.; Miura, H.; Itaka, K.; Ohara, S. Enhanced Antibacterial Property of Facet-Engineered TiO2 Nanosheet in Presence and Absence of Ultraviolet Irradiation. Materials 2020, 13, 78. [Google Scholar] [CrossRef]
  52. Moon, E.W.; Lee, H.-W.; Rok, J.H.; Ha, J.-H. Photocatalytic inactivation of viral particles of human norovirus by Cu-doped TiO2 non-woven fabric under UVA-LED wavelengths. Sci. Total Environ. 2020, 749, 141574. [Google Scholar] [CrossRef]
  53. Li, X.Y.; Xie, J.G.; Liao, L.Y.; Jiang, X.; Fu, H.Q. UV-curable polyurethane acrylate-Ag/TiO2 nanocomposites with superior UV light antibacterial activity. Int. J. Polym. Mater. Polym. Biomater. 2017, 66, 835–843. [Google Scholar] [CrossRef]
  54. Stoyanova, A.M.; Hitkova, H.Y.; Ivanova, N.K.; Bachvarova-Nedelcheva, A.D.; Iordanova, R.S.; Sredkova, M.P. Photocatalytic and antibacterial activity of Fe-doped TiO2 nanoparticles prepared by nonhydrolytic sol-gel method. Bulg. Chem. Commun. 2013, 45, 497–504. [Google Scholar]
  55. Koe, W.S.; Lee, J.W.; Chong, W.C.; Pang, Y.L.; Sim, L.C. An overview of photocatalytic degradation: Photocatalysts, mechanisms, and development of photocatalytic membrane. Environ. Sci. Pollut. Res. 2020, 27, 2522–2565. [Google Scholar] [CrossRef] [PubMed]
  56. Etacheri, V.; Di Valentin, C.; Schneider, J.; Bahnemann, D.; Pillai, S.C. Visible-light activation of TiO2 photocatalysts: Advances in theory and experiments. J. Photochem. Photobiol. C-Photochem. Rev. 2015, 25, 1–29. [Google Scholar] [CrossRef]
  57. Chakhtouna, H.; Benzeid, H.; Zari, N.; Qaiss, A.e.K.; Bouhfid, R. Recent progress on Ag/TiO2 photocatalysts: Photocatalytic and bactericidal behaviors. Environ. Sci. Pollut. Res. 2021, 28, 44638–44666. [Google Scholar] [CrossRef] [PubMed]
  58. Wysocka, I.; Kowalska, E.; Ryl, J.; Nowaczyk, G.; Zielinska-Jurek, A. Morphology, Photocatalytic and Antimicrobial Properties of TiO2 Modified with Mono- and Bimetallic Copper, Platinum and Silver Nanoparticles. Nanomaterials 2019, 9, 1129. [Google Scholar] [CrossRef] [PubMed]
  59. Moon, K.-S.; Choi, E.-J.; Bae, J.-M.; Park, Y.-B.; Oh, S. Visible Light-Enhanced Antibacterial and Osteogenic Functionality of Au and Pt Nanoparticles Deposited on TiO2 Nanotubes. Materials 2020, 13, 3721. [Google Scholar] [CrossRef]
  60. Lee, H.; Jang, H.S.; Kim, N.Y.; Joo, J.B. Cu-doped TiO2 hollow nanostructures for the enhanced photocatalysis under visible light conditions. J. Ind. Eng. Chem. 2021, 99, 352–363. [Google Scholar] [CrossRef]
  61. Meng, D.; Liu, X.; Xie, Y.; Du, Y.; Yang, Y.; Xiao, C. Antibacterial Activity of Visible Light-Activated TiO2 Thin Films with Low Level of Fe Doping. Adv. Mater. Sci. Eng. 2019, 2019, 5819805. [Google Scholar] [CrossRef]
  62. Gomez-Polo, C.; Larumbe, S.; Gil, A.; Munoz, D.; Fernandez, L.R.; Barquin, L.F.; Garcia-Prieto, A.; Fdez-Gubieda, M.L.; Muela, A. Improved photocatalytic and antibacterial performance of Cr doped TiO2 nanoparticles. Surf. Interfaces 2021, 22, 100867. [Google Scholar] [CrossRef]
  63. Yoo, S.M.; Rawal, S.B.; Lee, J.E.; Kim, J.; Ryu, H.-Y.; Park, D.-W.; Lee, W.I. Size-dependence of plasmonic Au nanoparticles in photocatalytic behavior of Au/TiO2 and Au@SiO2/TiO2. Appl. Catal. A-Gen. 2015, 499, 47–54. [Google Scholar] [CrossRef]
  64. Lin, Z.; Wang, X.; Liu, J.; Tian, Z.; Dai, L.; He, B.; Han, C.; Wu, Y.; Zeng, Z.; Hu, Z. On the role of localized surface plasmon resonance in UV-Vis light irradiated Au/TiO2 photocatalysis systems: Pros and cons. Nanoscale 2015, 7, 4114–4123. [Google Scholar] [CrossRef] [PubMed]
  65. Mukherjee, K.; Acharya, K.; Biswas, A.; Jana, N.R. TiO2 Nanoparticles Co-doped with Nitrogen and Fluorine as Visible-Light-Activated Antifungal Agents. ACS Appl. Nano Mater. 2020, 3, 2016–2025. [Google Scholar] [CrossRef]
  66. Wong, M.-S.; Sun, M.-T.; Sun, D.-S.; Chang, H.-H. Visible-Light-Responsive Antibacterial Property of Boron-Doped Titania Films. Catalysts 2020, 10, 1349. [Google Scholar] [CrossRef]
  67. Sun, D.-S.; Kau, J.-H.; Huang, H.-H.; Tseng, Y.-H.; Wu, W.-S.; Chang, H.-H. Antibacterial Properties of Visible-Light-Responsive Carbon-Containing Titanium Dioxide Photocatalytic Nanoparticles against Anthrax. Nanomaterials 2016, 6, 237. [Google Scholar] [CrossRef]
  68. Islam, S.Z.; Nagpure, S.; Kim, D.Y.; Rankin, S.E. Synthesis and Catalytic Applications of Non-Metal Doped Mesoporous Titania. Inorganics 2017, 5, 15. [Google Scholar] [CrossRef]
  69. Koli, V.B.; Ke, S.-C.; Dodamani, A.G.; Deshmukh, S.P.; Kim, J.-S. Boron-Doped TiO2-CNT Nanocomposites with Improved Photocatalytic Efficiency toward Photodegradation of Toluene Gas and Photo-Inactivation of Escherichia coli. Catalysts 2020, 10, 632. [Google Scholar] [CrossRef]
  70. Kilic, A.; Beyazsakal, L.; Findik, B.T.; Incebay, H. Synthesis and electrochemical investigation of chiral amine bis(phenolate)- boron complexes: In vitro antibacterial activity screening of boron compounds. Inorg. Chim. Acta 2020, 510, 119777. [Google Scholar] [CrossRef]
  71. Wang, Y.Z.; Wu, Y.S.; Yang, H.; Wang, M.; Shi, X.G.; Wang, C.; Zhang, S.W. Effect of calcination temperature on the microstructure and antimicrobial activity of boron and cerium co-doped titania nanomaterials. Mater. Technol. 2018, 33, 48–56. [Google Scholar] [CrossRef]
  72. Raja, A.; Selvakumar, K.; Rajasekaran, P.; Arunpandian, M.; Ashokkumar, S.; Kaviyarasu, K.; Bahadur, S.A.; Swaminathan, M. Visible active reduced graphene oxide loaded titania for photodecomposition of ciprofloxacin and its antibacterial activity. Colloids Surf. A-Physicochem. Eng. Asp. 2019, 564, 23–30. [Google Scholar] [CrossRef]
  73. Nasr, M.; Balme, S.; Eid, C.; Habchi, R.; Miele, P.; Bechelany, M. Enhanced Visible-Light Photocatalytic Performance of Electrospun rGO/TiO2 Composite Nanofibers. J. Phys. Chem. C 2017, 121, 261–269. [Google Scholar] [CrossRef]
  74. Li, H.; Wu, J.; Gao, X.; Li, T.; Zhang, M.; Niu, X.; Zhang, D.; Wang, Y.; Fan, H.; Wang, K. Preparation and Performance Study of Antibacterial Materials Based on GO-TiO2. Chemistryselect 2021, 6, 7880–7886. [Google Scholar] [CrossRef]
  75. Wu, Y.; Zang, Y.; Xu, L.; Wang, J.; Jia, H.; Miao, F. Synthesis of high-performance conjugated microporous polymer/TiO2 photocatalytic antibacterial nanocomposites. Mater. Sci. Eng. C-Mater. Biol. Appl. 2021, 126, 112121. [Google Scholar] [CrossRef] [PubMed]
  76. Kubiak, A.; Kubacka, M.; Gabala, E.; Dobrowolska, A.; Synoradzki, K.; Siwinska-Ciesielczyk, K.; Czaczyk, K.; Jesionowski, T. Hydrothermally Assisted Fabrication of TiO2-Fe3O4 Composite Materials and Their Antibacterial Activity. Materials 2020, 13, 4715. [Google Scholar] [CrossRef] [PubMed]
  77. Tekin, D.; Birhan, D.; Kiziltas, H. Thermal, photocatalytic, and antibacterial properties of calcinated nano-TiO2/polymer composites. Mater. Chem. Phys. 2020, 251, 123067. [Google Scholar] [CrossRef]
  78. Yuan, C.; Hung, C.-H.; Yuan, C.-S.; Li, H.-W. Preparation and Application of Immobilized Surfactant-Modified PANi-CNT/TiO2 under Visible-Light Irradiation. Materials 2017, 10, 877. [Google Scholar] [CrossRef]
  79. Saravanan, R.; Aviles, J.; Gracia, F.; Mosquera, E.; Gupta, V.K. Crystallinity and lowering band gap induced visible light photocatalytic activity of TiO2/CS (Chitosan) nanocomposites. Int. J. Biol. Macromol. 2018, 109, 1239–1245. [Google Scholar] [CrossRef]
  80. Wang, Q.; Ji, S.; Li, S.; Zhou, X.; Yin, J.; Liu, P.; Shi, W.; Wu, M.; Shen, L. Electrospinning visible light response Bi2MoO6/Ag3PO4 composite photocatalytic nanofibers with enhanced photocatalytic and antibacterial activity. Appl. Surf. Sci. 2021, 569, 150955. [Google Scholar] [CrossRef]
  81. Velempini, T.; Prabakaran, E.; Pillay, K. Recent developments in the use of metal oxides for photocatalytic degradation of pharmaceutical pollutants in water—A review. Mater. Today Chem. 2021, 19, 100380. [Google Scholar] [CrossRef]
  82. Yan, Y.; Li, C.Q.; Wu, Y.H.; Gao, J.K.; Zhang, Q.C. From isolated Ti-oxo clusters to infinite Ti-oxo chains and sheets: Recent advances in photoactive Ti-based MOFs. J. Mater. Chem. A 2020, 8, 15245–15270. [Google Scholar] [CrossRef]
  83. Du, Y.; Tang, D.; Zhang, G.; Wu, X. Facile synthesis of Ag2O-TiO2/sepiolite composites with enhanced visible-light photocatalytic properties. Chin. J. Catal. 2015, 36, 2219–2228. [Google Scholar] [CrossRef]
  84. Ton, N.Q.T.; Le, T.N.T.; Kim, S.; Dao, V.A.; Yi, J.; Vu, T.H.T. High-Efficiency Photo-Generated Charges of ZnO/TiO2 Heterojunction Thin Films for Photocatalytic and Antibacterial Performance. J. Nanosci. Nanotechnol. 2020, 20, 2214–2222. [Google Scholar] [CrossRef] [PubMed]
  85. Liu, B.; Mu, L.; Han, B.; Zhang, J.; Shi, H. Fabrication of TiO2/Ag2O heterostructure with enhanced photocatalytic and antibacterial activities under visible light irradiation. Appl. Surf. Sci. 2017, 396, 1596–1603. [Google Scholar] [CrossRef]
  86. Kiwi, J.; Rtimi, S. Mechanisms of the Antibacterial Effects of TiO2-FeOx under Solar or Visible Light: Schottky Barriers versus Surface Plasmon Resonance. Coatings 2018, 8, 391. [Google Scholar] [CrossRef]
  87. Janczarek, M.; Endo, M.; Zhang, D.; Wang, K.; Kowalska, E. Enhanced Photocatalytic and Antimicrobial Performance of Cuprous Oxide/Titania: The Effect of Titania Matrix. Materials 2018, 11, 2069. [Google Scholar] [CrossRef] [PubMed]
  88. Yao, X.Y.; Zhang, B.; Cui, S.; Yang, S.; Tang, X.N. Fabrication of SnSO4-modified TiO2 for enhance degradation performance of methyl orange (MO) and antibacterial activity. Appl. Surf. Sci. 2021, 551, 149419. [Google Scholar] [CrossRef]
  89. Endo, M.; Wei, Z.; Wang, K.; Karabiyik, B.; Yoshiiri, K.; Rokicka, P.; Ohtani, B.; Markowska-Szczupak, A.; Kowalska, E. Noble metal-modified titania with visible-light activity for the decomposition of microorganisms. Beilstein J. Nanotechnol. 2018, 9, 829–841. [Google Scholar] [CrossRef] [PubMed]
  90. Hajipour, P.; Eslami, A.; Bahrami, A.; Hosseini-Abari, A.; Saber, F.Y.; Mohammadi, R.; Mehr, M.Y. Surface modification of TiO2 nanoparticles with CuO for visible-light antibacterial applications and photocatalytic degradation of antibiotics. Ceram. Int. 2021, 47, 33875–33885. [Google Scholar] [CrossRef]
  91. Gapusan, R.B.; Balela, M.D.L. Visible light-induced photocatalytic and antibacterial activity of TiO2/polyaniline-kapok fiber nanocomposite. Polym. Bull. 2021, 47, 33875–33885. [Google Scholar] [CrossRef]
  92. Liang, Y.; Li, W.; Wang, X.; Zhou, R.; Ding, H. TiO2-ZnO/Au ternary heterojunction nanocomposite: Excellent antibacterial property and visible-light photocatalytic hydrogen production efficiency. Ceram. Int. 2022, 48, 2826–2832. [Google Scholar] [CrossRef]
  93. Collin, F. Chemical Basis of Reactive Oxygen Species Reactivity and Involvement in Neurodegenerative Diseases. Int. J. Mol. Sci. 2019, 20, 2407. [Google Scholar] [CrossRef]
  94. Selvam, S.; Sundrarajan, M. Functionalization of cotton fabric with PVP/ZnO nanoparticles for improved reactive dyeability and antibacterial activity. Carbohydr. Polym. 2012, 87, 1419–1424. [Google Scholar] [CrossRef]
  95. Guo, M.Y.; Ng, A.M.C.; Liu, F.Z.; Djurisic, A.B.; Chan, W.K. Photocatalytic activity of metal oxides-The role of holes and OH center dot radicals. Appl. Catal. B -Environ. 2011, 107, 150–157. [Google Scholar] [CrossRef]
  96. Guo, M.Y.; Ng, A.M.C.; Liu, F.Z.; Djurisic, A.B.; Chan, W.K.; Su, H.M.; Wong, K.S. Effect of Native Defects on Photocatalytic Properties of ZnO. J. Phys. Chem. C 2011, 115, 11095–11101. [Google Scholar] [CrossRef]
  97. Yu, J.L.; Tahmasebi, A.; Han, Y.; Yin, F.; Li, X. A review on water in low rank coals: The existence, interaction with coal structure and effects on coal utilization. Fuel Processing Technol. 2013, 106, 9–20. [Google Scholar] [CrossRef]
  98. Yougbare, S.; Mutalik, C.; Okoro, G.; Lin, I.H.; Krisnawati, D.I.; Jazidie, A.; Nuh, M.; Chang, C.C.; Kuo, T.R. Emerging Trends in Nanomaterials for Antibacterial Applications. Int. J. Nanomed. 2021, 16, 5831–5867. [Google Scholar] [CrossRef]
  99. Aruoja, V.; Dubourguier, H.-C.; Kasemets, K.; Kahru, A. Toxicity of nanoparticles of CuO, ZnO and TiO2 to microalgae Pseudokirchneriella subcapitata. Sci. Total Environ. 2009, 407, 1461–1468. [Google Scholar] [CrossRef]
  100. Li, K.; Chen, Y.; Zhang, W.; Pu, Z.; Jiang, L.; Chen, Y. Surface Interactions Affect the Toxicity of Engineered Metal Oxide Nanoparticles toward Paramecium. Chem. Res. Toxicol. 2012, 25, 1675–1681. [Google Scholar] [CrossRef]
  101. Agmon, E.; Solon, J.; Bassereau, P.; Stockwell, B.R. Modeling the effects of lipid peroxidation during ferroptosis on membrane properties. Sci. Rep. 2018, 8, 5515. [Google Scholar] [CrossRef]
  102. Hossein, M.M.; Potash, S.A.; Takikawa, M.; Shubhra, R.D.; Saha, T.; Islam, Z.; Hossein, S.; Hasan, M.A.; Takeoka, S.; Sarker, S.R. Investigation of the Antibacterial Activity and in vivo Cytotoxicity of Biogenic Silver Nanoparticles as Potent Therapeutics. Front. Bioeng. Biotechnol. 2019, 7, 239. [Google Scholar] [CrossRef]
  103. Niloy, M.S.; Hossain, M.M.; Takikawa, M.; Shakil, M.S.; Polash, S.A.; Mahmud, K.M.; Uddin, M.F.; Alam, M.; Shubhra, R.D.; Shawan, M.; et al. Synthesis of Biogenic Silver Nanoparticles Using Caesalpinia digyna and Investigation of Their Antimicrobial Activity and In Vivo Biocompatibility. ACS Appl. Bio Mater. 2020, 3, 7722–7733. [Google Scholar] [CrossRef]
  104. Yan, B.; Ai, Y.W.; Sun, Q.; Ma, Y.; Cao, Y.; Wang, J.W.; Zhang, Z.Y.; Wang, X.D. Membrane Damage during Ferroptosis Is Caused by Oxidation of Phospholipids Catalyzed by the Oxidoreductases POR and CYB5R1. Mol. Cell 2021, 81, 355–369.e10. [Google Scholar] [CrossRef] [PubMed]
  105. Shi, L.-E.; Li, Z.-H.; Zheng, W.; Zhao, Y.-F.; Jin, Y.-F.; Tang, Z.-X. Synthesis, antibacterial activity, antibacterial mechanism and food applications of ZnO nanoparticles: A review. Food Addit. Contam. Part A -Chem. Anal. Control Expo. Risk Assess. 2014, 31, 173–186. [Google Scholar] [CrossRef] [PubMed]
  106. Xu, X.; Yi, Z.; Chen, D.; Duan, X.; Zhou, Z.; Fan, X.; Jiang, M. Evaluation of photocatalytic production of active oxygen and decomposition of phenol in ZnO suspensions. Rare Met. 2011, 30, 188–191. [Google Scholar] [CrossRef]
  107. Yang, C.; Li, Q.; Tang, L.; Xin, K.; Bai, A.; Yu, Y. Synthesis, photocatalytic activity, and photogenerated hydroxyl radicals of monodisperse colloidal ZnO nanospheres. Appl. Surf. Sci. 2015, 357, 1928–1938. [Google Scholar] [CrossRef]
  108. Zhao, Y.; Li, J.; Wang, L.; Hao, Y.; Yang, L.; He, P.; Xue, J. Preparation and Characterization of Sulfated TiO2/zeolite Composite Catalysts with Enhanced Photocatalytic Activity. Nano 2018, 13, 49–59. [Google Scholar] [CrossRef]
  109. Gao, X.D.; Fei, G.T.; Xu, S.H.; Zhong, B.N.; Ouyang, H.M.; Li, X.H.; Zhang, L.D. Porous Ag/TiO2-Schottky-diode based plasmonic hot-electron photodetector with high detectivity and fast response. Nanophotonics 2019, 8, 1247–1254. [Google Scholar] [CrossRef]
  110. Mandal, S.S.; Bhattacharyya, A.J. Electrochemical sensing and photocatalysis using Ag-TiO2 microwires. J. Chem. Sci. 2012, 124, 969–978. [Google Scholar] [CrossRef]
  111. Hajjaji, A.; Elabidi, M.; Trabelsi, K.; Assadi, A.A.; Bessais, B.; Rtimi, S. Bacterial adhesion and inactivation on Ag decorated TiO2-nanotubes under visible light: Effect of the nanotubes geometry on the photocatalytic activity. Colloids Surf. B -Biointerfaces 2018, 170, 92–98. [Google Scholar] [CrossRef]
  112. Liu, J.; Wang, Y.; Ma, J.; Peng, Y.; Wang, A. A review on bidirectional analogies between the photocatalysis and antibacterial properties of ZnO. J. Alloys Compd. 2019, 783, 898–918. [Google Scholar] [CrossRef]
  113. Cadet, J.; Teoule, R. Comparative study of oxidation of nucleic acid components by hydroxyl radicals, singlet oxygen and superoxide anion radicals. Photochem. Photobiol. 1978, 28, 661–667. [Google Scholar] [CrossRef]
  114. Chen, B.B.; Pan, N.L.; Liao, J.X.; Huang, M.Y.; Jiang, D.C.; Wang, J.J.; Qiu, H.J.; Chen, J.X.; Li, L.; Sun, J. Cyclometalated iridium(III) complexes as mitochondria-targeted anticancer and antibacterial agents to induce both autophagy and apoptosis. J. Inorg. Biochem. 2021, 219, 111450. [Google Scholar] [CrossRef] [PubMed]
  115. Rajendran, R.; Mani, A. Photocatalytic, antibacterial and anticancer activity of silver-doped zinc oxide nanoparticles. J. Saudi Chem. Soc. 2020, 24, 1010–1024. [Google Scholar] [CrossRef]
  116. Zhang, X.; Xiao, G.; Wang, Y.; Zhao, Y.; Su, H.; Tan, T. Preparation of chitosan-TiO2 composite film with efficient antimicrobial activities under visible light for food packaging applications. Carbohydr. Polym. 2017, 169, 101–107. [Google Scholar] [CrossRef] [PubMed]
  117. Tong, T.Z.; Binh, C.T.T.; Kelly, J.J.; Gaillard, J.F.; Gray, K.A. Cytotoxicity of commercial nano-TiO2 to Escherichia coli assessed by high-throughput screening: Effects of environmental factors. Water Res. 2013, 47, 2352–2362. [Google Scholar] [CrossRef]
  118. Li, H.Y.; Gao, Y.C.; Li, C.X.; Ma, G.; Shang, Y.L.; Sun, Y. A comparative study of the antibacterial mechanisms of silver ion and silver nanoparticles by Fourier transform infrared spectroscopy. Vib. Spectrosc. 2016, 85, 112–121. [Google Scholar] [CrossRef]
  119. Shaligram, S.; Campbell, A. Toxicity of copper salts is dependent on solubility profile and cell type tested. Toxicol. Vitr. 2013, 27, 844–851. [Google Scholar] [CrossRef]
  120. Chang, L.; Duan, W.J.; Chen, A.G.; Li, J.J.; Huang, S.Q.; Tang, H.J.; Pan, G.; Deng, Y.; Zhao, L.N.; Li, D.F.; et al. Preparation of polyacrylonitrile-based fibres with chelated Ag ions for antibacterial applications. R. Soc. Open Sci. 2020, 7, 200324. [Google Scholar] [CrossRef]
  121. Saidin, S.; Jumat, M.A.; Amin, N.; Al-Hammadi, A.S.S. Organic and inorganic antibacterial approaches in combating bacterial infection for biomedical application. Mat. Sci. Eng. C-Mater. 2021, 118, 111382. [Google Scholar] [CrossRef]
  122. Shi, A.Q.; Zhu, C.S.; Fu, S.; Wang, R.X.; Qin, G.W.; Chen, D.F.; Zhang, E.L. What controls the antibacterial activity of Ti-Ag alloy, Ag ion or Ti2Ag particles? Mater. Sci. Eng. C-Mater. Biol. Appl. 2020, 109, 110548. [Google Scholar] [CrossRef]
  123. Hou, J.; Wang, L.; Wang, C.; Zhang, S.; Liu, H.; Li, S.; Wang, X. Toxicity and mechanisms of action of titanium dioxide nanoparticles in living organisms. J. Environ. Sci. 2019, 75, 40–53. [Google Scholar] [CrossRef]
  124. Fenno, L.; Yizhar, O.; Deisseroth, K. The development and application of optogenetics. Annu. Rev. Neurosci. 2010, 34, 389–412. [Google Scholar] [CrossRef]
  125. Jones, N.; Ray, B.; Ranjit, K.T.; Manna, A.C. Antibacterial activity of ZnO nanoparticle suspensions on a broad spectrum of microorganisms. Fems Microbiol. Lett. 2008, 279, 71–76. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  126. Applerot, G.; Lipovsky, A.; Dror, R.; Perkas, N.; Nitzan, Y.; Lubart, R.; Gedanken, A. Enhanced Antibacterial Activity of Nanocrystalline ZnO Due to Increased ROS-Mediated Cell Injury. Adv. Funct. Mater. 2009, 19, 842–852. [Google Scholar] [CrossRef]
  127. Wahab, R.; Siddiqui, M.A.; Saquib, Q.; Dwivedi, S.; Ahmad, J.; Musarrat, J.; Al-Khedhairy, A.A.; Shin, H.-S. ZnO nanoparticles induced oxidative stress and apoptosis in HepG2 and MCF-7 cancer cells and their antibacterial activity. Colloids Surf. B -Biointerfaces 2014, 117, 267–276. [Google Scholar] [CrossRef]
  128. Engineering, F. Antimicrobial materials, coatings and biomimetic surfaces with modified microtography to control microbial fouling of product contact surfaces within food processing equipment: Legislation, requirements, effectiveness and challenges. J. Hyg. Eng. Des. 2014, 7, 8–29. [Google Scholar]
  129. Liao, C.; Li, Y.; Tjong, S.C. Visible-Light Active Titanium Dioxide Nanomaterials with Bactericidal Properties. Nanomaterials 2020, 10, 124. [Google Scholar] [CrossRef]
  130. Yuan, X.; Wei, Q.; Ke, H.; Huang, Z.; Chen, D. Structural color and photocatalytic property of polyester fabrics coated with Ag/ZnO composite films. Int. J. Cloth. Sci. Technol. 2019, 31, 487–494. [Google Scholar] [CrossRef]
  131. Akyildiz, H.I.; Diler, S.; Islam, S. Evaluation of TiO2 and ZnO atomic layer deposition coated polyamide 66 fabrics for photocatalytic activity and antibacterial applications. J. Vac. Sci. Technol. A 2021, 39, 022405. [Google Scholar] [CrossRef]
  132. Schneider, J.; Matsuoka, M.; Takeuchi, M.; Zhang, J.L.; Horiuchi, Y.; Anpo, M.; Bahnemann, D.W. Understanding TiO2 Photocatalysis: Mechanisms and Materials. Chem. Rev. 2014, 114, 9919–9986. [Google Scholar] [CrossRef]
  133. Lim, E.S.; Kim, J.J.; Sul, W.J.; Kim, J.S.; Kim, B.; Kim, H.; Koo, O.K. Metagenomic Analysis of Microbial Composition Revealed Cross-Contamination Pathway of Bacteria at a Foodservice Facility. Front. Microbiol. 2021, 12, 636329. [Google Scholar] [CrossRef]
  134. Olatunde, O.O.; Benjakul, S. Nonthermal Processes for Shelf-Life Extension of Seafoods: A Revisit. Compr. Rev. Food Sci. Food Saf. 2018, 17, 892–904. [Google Scholar] [CrossRef] [PubMed]
  135. Wu, D.; Forghani, F.; Daliri, E.B.-M.; Li, J.; Liao, X.; Liu, D.; Ye, X.; Chen, S.; Ding, T. Microbial response to some nonthermal physical technologies. Trends Food Sci. Technol. 2020, 95, 107–117. [Google Scholar] [CrossRef]
  136. Ekezie, F.-G.C.; Cheng, J.-H.; Sun, D.-W. Effects of nonthermal food processing technologies on food allergens: A review of recent research advances. Trends Food Sci. Technol. 2018, 74, 12–25. [Google Scholar] [CrossRef]
  137. Goudarzi, V.; Shahabi-Ghahfarrokhi, I.; Babaei-Ghazvini, A. Preparation of ecofriendly UV-protective food packaging material by starch/TiO2 bio-nanocomposite: Characterization. Int. J. Biol. Macromol. 2017, 95, 306–313. [Google Scholar] [CrossRef]
  138. Duan, N.; Li, Q.; Meng, X.; Wang, Z.; Wu, S. Preparation and characterization of k-carrageenan/konjac glucomannan/TiO2 nanocomposite film with efficient anti-fungal activity and its application in strawberry preservation. Food Chem. 2021, 364, 130441. [Google Scholar] [CrossRef]
  139. Roman, L.E.; Huachani, J.; Uribe, C.; Solis, J.L.; Gomez, M.M.; Costa, S.; Costa, S. Blocking erythemally weighted UV radiation using cotton fabrics functionalized with ZnO nanoparticles in situ. Appl. Surf. Sci. 2019, 469, 204–212. [Google Scholar] [CrossRef]
  140. Tian, H.; Zhai, Y.; Xu, C.; Liang, J. Durable Antibacterial Cotton Fabrics Containing Stable Acyclic N-Halamine Groups. Ind. Eng. Chem. Res. 2017, 56, 7902–7909. [Google Scholar] [CrossRef]
  141. Xu, J.; Jiang, S.X.; Peng, L.; Wang, Y.; Shang, S.; Miao, D.; Guo, R. AgNps-PVA-coated woven cotton fabric: Preparation, water repellency, shielding properties and antibacterial activity. J. Ind. Text. 2019, 48, 1545–1565. [Google Scholar] [CrossRef]
  142. Ranjbar-Mohammadi, M. Production of cotton fabrics with durable antibacterial property by using gum tragacanth and silver. Int. J. Biol. Macromol. 2018, 109, 476–482. [Google Scholar] [CrossRef]
  143. Zhu, Y.; Mao, K.L.; Rong, J.; Zheng, Y.H.; Yang, D.Y.; Zhang, T.; Qiu, F.X. Fabrication of titanium incorporation into zeolitic imidazolate framework-L on fabric carrier for visible-light driven photocatalytic antibacterial activity. Opt. Mater. 2022, 125, 112085. [Google Scholar] [CrossRef]
  144. Biswas, A.; Jana, N.R. Cotton Modified with Silica Nanoparticles, N,F Codoped TiO2 Nanoparticles, and Octadecyltrimethoxysilane for Textiles with Self-Cleaning and Visible Light-Based Cleaning Properties. ACS Appl. Nano Mater. 2021, 4, 877–885. [Google Scholar] [CrossRef]
  145. Yuzer, B.; Aydin, M.I.; Con, A.H.; Inan, H.; Can, S.; Selcuk, H.; Kadmi, Y. Photocatalytic, self-cleaning and antibacterial properties of Cu(II) doped TiO2. J. Environ. Manag. 2022, 302, 114023. [Google Scholar] [CrossRef] [PubMed]
  146. Verdier, T.; Bertron, A.; Erable, B.; Roques, C. Bacterial Biofilm Characterization and Microscopic Evaluation of the Antibacterial Properties of a Photocatalytic Coating Protecting Building Material. Coatings 2018, 8, 93. [Google Scholar] [CrossRef] [Green Version]
  147. Janus, M.; Kusiak-Nejman, E.; Rokicka-Konieczna, P.; Markowska-Szczupak, A.; Zajac, K.; Morawski, A.W. Bacterial Inactivation on Concrete Plates Loaded with Modified TiO2 Photocatalysts under Visible Light Irradiation. Molecules 2019, 24, 3026. [Google Scholar] [CrossRef] [PubMed]
  148. He, J.; Cheng, J.; Lo, I.M.C. Green photocatalytic disinfection of real sewage: Efficiency evaluation and toxicity assessment of eco-friendly TiO2-based magnetic photocatalyst under solar light. Water Res. 2021, 190, 116705. [Google Scholar] [CrossRef]
  149. Tshangana, C.; Chabalala, M.; Muleja, A.; Nxumalo, E.; Mamba, B. Shape-dependant photocatalytic and antimicrobial activity of ZnO nanostructures when conjugated to graphene quantum dots. J. Environ. Chem. Eng. 2020, 8, 103930. [Google Scholar] [CrossRef]
  150. Sen Chang, J.; Chong, M.N.; Poh, P.E.; Ocon, J.D.; Zoqratt, M.Z.H.M.; Lee, S.M. Impacts of morphological-controlled ZnO nanoarchitectures on aerobic microbial communities during real wastewater treatment in an aerobic-photocatalytic system. Environ. Pollut. 2020, 259, 113867. [Google Scholar] [CrossRef]
  151. Melinte, V.; Buruiana, T.; Rosca, I.; Chibac, A.L. TiO2-Based Photopolymerized Hybrid Catalysts with Visible Light Catalytic Activity Induced by In Situ Generated Ag/Au NPs. Chemistryselect 2019, 4, 5138–5149. [Google Scholar] [CrossRef]
  152. Si, Y.; Liu, H.; Yu, H.; Jiang, X.; Sun, D. A heterogeneous TiO2/SrTiO3 coating on titanium alloy with excellent photocatalytic antibacterial, osteogenesis and tribocorrosion properties. Surf. Coat. Technol. 2022, 431, 128008. [Google Scholar] [CrossRef]
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Figure 1. Statistical analysis of the number of related papers published in Web of Science with the keywords: (A) ‘Photocatalyst’ and (B) ‘Photocatalytic antimicrobial’.
Figure 1. Statistical analysis of the number of related papers published in Web of Science with the keywords: (A) ‘Photocatalyst’ and (B) ‘Photocatalytic antimicrobial’.
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Figure 3. (A) SEM (a) and AFM (b) analyses of different samples; (B) SEM micrographs of biofilms formed on different samples; (C) Colony-forming units (CFUs) on surfaces of different sample after 1 h of UVA light irradiation [48].
Figure 3. (A) SEM (a) and AFM (b) analyses of different samples; (B) SEM micrographs of biofilms formed on different samples; (C) Colony-forming units (CFUs) on surfaces of different sample after 1 h of UVA light irradiation [48].
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Figure 4. (A) SEM images of E. coli before (a,b) and after (c,d) TiO2@SiO2 treatment; (B) image of the antibacterial effect of TiO2@SiO2 hybrid materials with different TiO2 contents on E. coli under UVA irradiation; (C) effect of the antimicrobial property of TiO2@SiO2 hybrid materials under UVA irradiation [50].
Figure 4. (A) SEM images of E. coli before (a,b) and after (c,d) TiO2@SiO2 treatment; (B) image of the antibacterial effect of TiO2@SiO2 hybrid materials with different TiO2 contents on E. coli under UVA irradiation; (C) effect of the antimicrobial property of TiO2@SiO2 hybrid materials under UVA irradiation [50].
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Figure 5. (A) antimicrobial activity in the dark (a) and under visible light (b) (λ > 450 nm) [58]; (B) TEM images of Au–TiO2 NTs (a) and Pt–TiO2 NTs (b); (C) photographs of antibacterial S. aureus agar diffusion tests (a) and the results of CFUs per unit volume of S. aureus cultured on different letters with or without 470 nm and 600 nm visible irradiation (b) [59].
Figure 5. (A) antimicrobial activity in the dark (a) and under visible light (b) (λ > 450 nm) [58]; (B) TEM images of Au–TiO2 NTs (a) and Pt–TiO2 NTs (b); (C) photographs of antibacterial S. aureus agar diffusion tests (a) and the results of CFUs per unit volume of S. aureus cultured on different letters with or without 470 nm and 600 nm visible irradiation (b) [59].
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Figure 6. (A) TEM image of N, F doped TiO2 nanoparticles (a); UV−vis absorption spectrum of colloidal nanoparticles (b); evidence of reactive oxygen species (ROS) generation by nanoparticles under visible-light exposure (c); tert-butyl alcohol (TBA) as a ·OH scavenger to prove that ·OH is the dominant ROS component (d); (B) microscopic imaging of Fusarium oxysporum spore germination under different conditions. Red arrows indicate fungal spores. (C) Images of fungal colonies [65].
Figure 6. (A) TEM image of N, F doped TiO2 nanoparticles (a); UV−vis absorption spectrum of colloidal nanoparticles (b); evidence of reactive oxygen species (ROS) generation by nanoparticles under visible-light exposure (c); tert-butyl alcohol (TBA) as a ·OH scavenger to prove that ·OH is the dominant ROS component (d); (B) microscopic imaging of Fusarium oxysporum spore germination under different conditions. Red arrows indicate fungal spores. (C) Images of fungal colonies [65].
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Figure 7. (A) SEM image of TiO2 (B) films with various thicknesses before (a–d) and after (e–h) annealing; (B) visible light-induced photolytic killing of pathogenic bacteria [66]; (C) antibacterial properties of C200 NPs against vegetative bacteria of Bacillus species; (D) antibacterial properties of C200 NPs against spores of Bacillus species [67]; (E) % survival of E. coli with TiO2TiO2TiO2different samples as a function of time under visible light; ## p < 0.01, ** p < 0.01, * p < 0.05. (F) photographs of the photoinactivation of E. coli under visible light exposure [69].
Figure 7. (A) SEM image of TiO2 (B) films with various thicknesses before (a–d) and after (e–h) annealing; (B) visible light-induced photolytic killing of pathogenic bacteria [66]; (C) antibacterial properties of C200 NPs against vegetative bacteria of Bacillus species; (D) antibacterial properties of C200 NPs against spores of Bacillus species [67]; (E) % survival of E. coli with TiO2TiO2TiO2different samples as a function of time under visible light; ## p < 0.01, ** p < 0.01, * p < 0.05. (F) photographs of the photoinactivation of E. coli under visible light exposure [69].
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Materials 15 05820 g008 550
Figure 8. (A) Photocatalytic inactivation of E. coli (a) and S. aureus using 13 wt% CMP/TiO2-I nanocomposites. Growth images of E. coli (b) and S. aureus on agar plates; (B) SEM images of bacteria (incubated with 13 wt% CMP/TiO2-I nanocomposites under light irradiation and in the dark); (C) DRS of samples [75].
Figure 8. (A) Photocatalytic inactivation of E. coli (a) and S. aureus using 13 wt% CMP/TiO2-I nanocomposites. Growth images of E. coli (b) and S. aureus on agar plates; (B) SEM images of bacteria (incubated with 13 wt% CMP/TiO2-I nanocomposites under light irradiation and in the dark); (C) DRS of samples [75].
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Materials 15 05820 g010 550
Figure 10. Schematic of photocatalytic antimicrobial mechanism of TiO2@SiO2 hybrid materials and bacterial inactivation on Ag decorated TiO2-NTs [50,111].
Figure 10. Schematic of photocatalytic antimicrobial mechanism of TiO2@SiO2 hybrid materials and bacterial inactivation on Ag decorated TiO2-NTs [50,111].
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Materials 15 05820 g011 550
Figure 11. (A) Proposed mechanism of the antifungal activity of N, F doped TiO2 nanoparticles [65]; (B) schematic diagram displaying the antibacterial mechanism of SnSO4-TiO2 [88].
Figure 11. (A) Proposed mechanism of the antifungal activity of N, F doped TiO2 nanoparticles [65]; (B) schematic diagram displaying the antibacterial mechanism of SnSO4-TiO2 [88].
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Materials 15 05820 g012 550
Figure 12. Schematic diagrams of the effect of metal ions (A [121]) and TiO2 (B [123]) particles on cells.
Figure 12. Schematic diagrams of the effect of metal ions (A [121]) and TiO2 (B [123]) particles on cells.
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Materials 15 05820 g013 550
Figure 13. (A) Effect of the prepared composite films on the growth of P. viridicatum after 0 h and 6 h of irradiation; (B) effects of TiO2 content on the inhibition efficiency of KC/KGM/TiO2 nanocomposite films against P. viridicatum [138]; (C) preservation of red grapes packed in different materials at 37 °C for 6 days [116]; (D) (a) in vivo fungitoxicity and infection control by nanoparticles. (b) Evidence of intact immunity of nanoparticle and visible-light-treated tomato fruit via nitric oxide imaging. Green fluorescence indicates the presence of nitric oxide [65].
Figure 13. (A) Effect of the prepared composite films on the growth of P. viridicatum after 0 h and 6 h of irradiation; (B) effects of TiO2 content on the inhibition efficiency of KC/KGM/TiO2 nanocomposite films against P. viridicatum [138]; (C) preservation of red grapes packed in different materials at 37 °C for 6 days [116]; (D) (a) in vivo fungitoxicity and infection control by nanoparticles. (b) Evidence of intact immunity of nanoparticle and visible-light-treated tomato fruit via nitric oxide imaging. Green fluorescence indicates the presence of nitric oxide [65].
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Materials 15 05820 g014 550
Figure 14. (A) Photographs of the antibacterial activity of Zn2+, H-MeIM and ZIF-L@TiO2/fabrics against E. coli; (B) photographs of bacterial growth on blank nontextile fabric and ZIF-L@TiO2/fabric under natural light for 1–5 days at 37 °C [143]; (C) nonwetting behavior of modified cotton (a) and paper (b) surface [144] paper; (D) self-cleaning performance of 1% Cu (II)-doped TiO2 calcined at 25 °C [145].
Figure 14. (A) Photographs of the antibacterial activity of Zn2+, H-MeIM and ZIF-L@TiO2/fabrics against E. coli; (B) photographs of bacterial growth on blank nontextile fabric and ZIF-L@TiO2/fabric under natural light for 1–5 days at 37 °C [143]; (C) nonwetting behavior of modified cotton (a) and paper (b) surface [144] paper; (D) self-cleaning performance of 1% Cu (II)-doped TiO2 calcined at 25 °C [145].
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Materials 15 05820 g015 550
Figure 15. (A) Epifluorescence images of surface samples after 24 h of the experiment (blue color represent the coating and red to highlight the bacteria) [146]; (B) photocatalytic disinfection performance of sewage samples and the light control tests of (c) HB and (d) HC under simulated solar light at 25 °C; and regrowth test of inactivated bacteria (24 h and 48 h after reaction) in (e) LT and (f) LB [148]; (C) schematic diagram of TiO2/SrTiO3 function; (D) bacteriostatic circles of different samples after 24 h [152].
Figure 15. (A) Epifluorescence images of surface samples after 24 h of the experiment (blue color represent the coating and red to highlight the bacteria) [146]; (B) photocatalytic disinfection performance of sewage samples and the light control tests of (c) HB and (d) HC under simulated solar light at 25 °C; and regrowth test of inactivated bacteria (24 h and 48 h after reaction) in (e) LT and (f) LB [148]; (C) schematic diagram of TiO2/SrTiO3 function; (D) bacteriostatic circles of different samples after 24 h [152].
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Shang, C.; Bu, J.; Song, C. Preparation, Antimicrobial Properties under Different Light Sources, Mechanisms and Applications of TiO2: A Review. Materials 2022, 15, 5820. https://doi.org/10.3390/ma15175820

AMA Style

Shang C, Bu J, Song C. Preparation, Antimicrobial Properties under Different Light Sources, Mechanisms and Applications of TiO2: A Review. Materials. 2022; 15(17):5820. https://doi.org/10.3390/ma15175820

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Shang, Changyu, Junyu Bu, and Cui Song. 2022. "Preparation, Antimicrobial Properties under Different Light Sources, Mechanisms and Applications of TiO2: A Review" Materials 15, no. 17: 5820. https://doi.org/10.3390/ma15175820

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