Recent Developments in Synthesis and Photocatalytic Applications of Carbon Dots

The tunable photoluminescent and photocatalytic properties of carbon dots (CDs) via chemical surface modification have drawn increased attention to this emerging class of carbon nanomaterials. Herein, we summarize the advances in CD synthesis and modification, with a focus on surface functionalization, element doping, passivation, and nanocomposite formation with metal oxides, transition metal chalcogenides, or graphitic carbon nitrides. The effects of CD size and functionalization on photocatalytic properties are discussed, along with the photocatalytic applications of CDs in energy conversion, water splitting, hydrogen evolution, water treatment, and chemical degradation. In particular, the enzyme-mimetic and photodynamic applications of CDs for bio-related uses are thoroughly reviewed.


Introduction to Carbon Dots (CDs)
Carbon dots (CDs) are discrete quasi-spherical carbon particles with sizes of <10 nm, normally having an sp 2 -conjugated carbon core with oxygenated functional groups, such as -OH, -COOH, and -CHO. The salient feature of CDs is their photoluminescence (PL), specifically, their excitation wavelength-(in)dependent emission [1]. Since 2006, CDs have been extensively researched due to their simple synthesis, low cost, abundance, excellent biocompatibility, and other advantages, and they have found diverse applications in the fields of (photo) catalysis, optoelectronics, energy storage/conversion, nanomedicine, sensing, and bioimaging [2]. More than half of these applications make use of the photoresponsive ability of CDs in a wide wavelength (ultraviolet to infrared) range and their outstanding electron transfer performance. The low toxicity and biocompatibility of CDs make them viable alternatives to heavy metal-based semiconducting quantum dots (QDs). Although the wide application scope of CDs necessitates the development of suitable large-scale synthesis methods, only few works have dealt with the mass production of CDs, as the ease of large-scale synthesis depends strongly on the intrinsic nature of raw materials [3]. This review focuses on scalable bottom-up CD syntheses offering the benefits of precisely controllable morphology and size distribution, as well as convenient surface passivation. The widespread hydrothermal CD synthesis techniques employ various organic molecules as precursors. Ana and Camacho [10] used two different cellulose-based materials, raw cellulose (RC) and nanocrystalline cellulose (NC), which were extracted from the green algae (Cladophora rupestris) as carbon sources to probe the effect of precursor size on the properties of CDs that were intended for application in solar cells. RC comprises compact amorphous fibers with a diameter of 0.53 ± 0.09 µm, while NC has a loose crystalline structure, containing particles with a diameter of 20.0 ± 4.4 nm. Notably, RC afforded smaller CDs (10.0 ± 3.74 nm) than NC (76.9 ± 73.1 nm), even though the former precursor had a larger particle size than the latter. This finding was mainly ascribed to the fact that the synthesis of CDs from NC was performed at a higher concentration, which favored the aggregation or clustering of the hydrophilic-surface CDs. RC-and NC-derived CDs both exhibited This review focuses on scalable bottom-up CD syntheses offering the benefits of precisely controllable morphology and size distribution, as well as convenient surface passivation. The widespread hydrothermal CD synthesis techniques employ various organic molecules as precursors. Ana and Camacho [10] used two different cellulose-based materials, raw cellulose (RC) and nanocrystalline cellulose (NC), which were extracted from the green algae (Cladophora rupestris) as carbon sources to probe the effect of precursor size on the properties of CDs that were intended for application in solar cells. RC comprises compact amorphous fibers with a diameter of 0.53 ± 0.09 µm, while NC has a loose crystalline structure, containing particles with a diameter of 20.0 ± 4.4 nm. Notably, RC afforded smaller CDs (10.0 ± 3.74 nm) than NC (76.9 ± 73.1 nm), even though the former A simple and rapid heating method was used to obtain CDs with QYs of up to 30% [9] from oligoethylenimine and β-cyclodextrin by incubation in a phosphoric acid/water mixture at 90 °C for only 2 h. CDs that were obtained after dialysis had a uniform spherical shape with diameters of 2-4 nm and they exhibited outstanding green fluorescence at 510 nm (excitation at 390 nm) with a QY of 30%. Table 1 summarizes methods of CD synthesis from different precursors as well as CD optical/physical properties and applications.  A simple and rapid heating method was used to obtain CDs with QYs of up to 30% [9] from oligoethylenimine and β-cyclodextrin by incubation in a phosphoric acid/water mixture at 90 • C for only 2 h. CDs that were obtained after dialysis had a uniform spherical shape with diameters of 2-4 nm and they exhibited outstanding green fluorescence at 510 nm (excitation at 390 nm) with a QY of 30%. Table 1 summarizes methods of CD synthesis from different precursors as well as CD optical/physical properties and applications. Catalysts 2020, 10, 320 6 of 23 Patents involving CDs synthesis and applications are few, as most related research deals with the synthesis and applications of metal-containing QDs. The first CD-related patent (filed in 2010) describes a method of producing water-soluble fluorescent carbon dots from carbon soot [24]. CDs with sizes of 2-7 nm were oxidatively treated to introduce hydrophilic surface carboxyl groups in amounts that are sufficient for fluorescence [24]. Another patent disclosed a single-step hydrothermal method of preparing water-soluble biomass-derived fluorescent CDs from cellulose and urea [25]. The prepared CDs were subjected to centrifugation, dialysis, and lyophilization to obtain solid-state CDs, which showed promising water solubility, low toxicity, good biocompatibility, and could be potentially used for cell imaging [25]. The recently described production of nitrogen-doped fluorescent CDs from milk at a moderate temperature (100-120 • C) within a short time (20-40 min.) [26] paves the way to the low-cost large-scale production of fluorescent CDs with a size distribution of 2-10 nm. In 2017, two patents describing the preparation of biomass-derived CDs were filed [27,28]. One of these patents describes a method comprising the consecutive steps of biomass impregnation and hydrothermal carbonization for 1-5 h at 150-350 • C in the presence of one or more activators, such as KOH, NaOH, K 2 CO 3 , KHCO 3 , Na 2 CO 3 , and NaHCO 3 [27], which affords CDs with a uniform size distribution and an average size of 5 nm. Another patent describes the synthesis of biomass tar-derived CDs via a catalytic reaction of a molecular sieve/tar mixture at 300-800 • C, followed by sonication [28], which provides well-dispersed CDs with a high QY. The categories of patents that are related to CDs are illustrated by the overall patent analysis and international patent classification (IPC) groups presented in Figure 3A. The top groups of filed patents and the numbers of filed patents, as demonstrated in Figure 3B, involve chemistry/metallurgy containing carbon, modified nanoparticles utilizing carbon source, co-doped carbon, biomass hydrothermal, and microwave synthesis for sun-light excitable carbon dots, as well as the application of CDs exhibiting luminescence, e.g., electroluminescence, chemiluminescence, photonics, and sensors, as well as CDs that are suitable for bio-related applications, such as imaging, dressing, and photothermal treatment.
In summary, the control of CD size, precursor dimensions, and additional chemicals, as well as their concentration to slow down the isotropic growth of particles, play crucial roles apart from synthesis conditions (e.g., temperature and time). CD photoluminescent properties can be effectively enhanced by reduction/oxidation with proper agents (e.g., NaBH 4 , nitric acid, and phosphoric acid). The size and reduction degree of CDs influence the blue shift of their fluorescence peaks, owing to the effects of surface plasmon resonance and quantum confinement. However, post-treatment and purification are required to obtain CDs with high stability, excellent QY, a narrow size distribution, and, hence, superior photoluminescent, optoelectronic, and photocatalytic properties. In summary, the control of CD size, precursor dimensions, and additional chemicals, as well as their concentration to slow down the isotropic growth of particles, play crucial roles apart from synthesis conditions (e.g., temperature and time). CD photoluminescent properties can be effectively enhanced by reduction/oxidation with proper agents (e.g., NaBH4, nitric acid, and phosphoric acid). The size and reduction degree of CDs influence the blue shift of their fluorescence peaks, owing to the effects of surface plasmon resonance and quantum confinement. However, post-treatment and purification are required to obtain CDs with high stability, excellent QY, a narrow size distribution, and, hence, superior photoluminescent, optoelectronic, and photocatalytic properties.

Modification and Photocatalytic Applications of CDs
The need for green, sustainable, and circular syntheses of chemicals and fuels has drawn much attention to photocatalytic processes, in which solar energy drives redox reactions. The band-gap structure and charge transfer ability of the corresponding photocatalyst is a vital factor influencing

Modification and Photocatalytic Applications of CDs
The need for green, sustainable, and circular syntheses of chemicals and fuels has drawn much attention to photocatalytic processes, in which solar energy drives redox reactions. The band-gap structure and charge transfer ability of the corresponding photocatalyst is a vital factor influencing the efficiency of a given reaction. Thus, the diversity and controllability of CD properties have inspired numerous works on the photocatalytic applications of CDs.
Photocatalytic processes comprise the stages of (i) light absorption and electron-hole pair generation, (ii) charge migration and transfer toward the photocatalyst surface, and (iii) incident reduction and oxidation at the photocatalyst surface due to the carried charges [29]. The spontaneous redox reactions occur at the photocatalyst surface. The rapid recombination of electrons and holes takes place, unless either oxygen or other electron acceptors scavenge the electrons to generate superoxide (O 2 •− ) and perhydroxyl (HOO • ) radicals and, subsequently, H 2 O 2 [30].
Band gap energy is of utmost importance in the design of high-performance photocatalysts, as this parameter needs to be equal to or lower than photon energy for the photocatalyst to be effective. As TiO 2 is a photocatalyst with wide band gap, it can only be excited by short-wavelength UV radiation. One should design photocatalysts absorbing light in a broad range of wavelengths, especially at visible-light or longer ones, to enhance the efficiency of solar light utilization. Visible light corresponds to photons with energies of 2.43-3.2 eV and, thus, the bandgap of visible-light-excitable photocatalysts should be less than the aforementioned photon energy [29]. Moreover, the photocatalyst valence band energy should be more positive than the oxidation potential, while the conduction band energy should be more negative than the reduction potential. The inherent electron-hole pair generation and migration toward the photocatalyst surface, as well as the photocatalyst surface states that facilitate charge trapping and transport, can substantially enhance photocatalytic performance. Consequently, the surface passivation and functionalization of photocatalysts are essential not only for increasing their efficiency, but also for enhancing their resistance to corrosion and dissociation that are caused by photogenerated intermediates [31].

Modification of CDs for Photocatalysis
The photocatalytic properties of CDs were first discovered in 2010 [32]: CDs that were synthesized by an alkali-assisted electrochemical method and featuring diameters of 1.2-3.8 nm showed outstanding size-dependent photoluminescent properties [32]. However, CD surface modification, the grafting of CDs onto other semiconductor photocatalysts, and/or composite formation are required to make CDs suitable for use as photocatalysts or photosensitizers.
Based on literature studies, the methods of modifying CDs for photocatalytic applications can be categorized into surface functionalization, passivation, element doping, and composite synthesis. Figure 4 illustrates the difference between CD surface functionalization and passivation. The surface functionalization of photocatalysts or photosensitizers can facilitate the separation of electrons and holes, prevent their recombination, and promote charge migration by trapping the photogenerated electrons at a variety of surface sites, which allows for one to control the kinetics of redox reactions. Various methods have been introduced to manipulate the surface functionalization of CDs, as exemplified by coordination/complexation techniques [33], sol-gel techniques [34], covalent bonding strategies, such as amide coupling [35], and π-π interactions [36]. Among the functionalization techniques, acyl chloride ligand exchange replaces carboxyl groups on the CD surface with amine groups. Typically, carboxyl-capped CDs that were hydrothermally synthesized from organic acids [37,38] are reacted with thionyl chloride under reflux to selectively convert surface carboxyl groups into acyl chloride groups and, thus, make CDs soluble in polar organic solvents, such as acetone, tetrahydrofuran, and acetonitrile. Thus, this functionalization facilitates the simple purification of CDs by solvent extraction [39], and the highly reactive acyl chloride groups can be additionally replaced with amine groups. In turn, the amino groups can be reacted with N,N-dimethylethylenediamine to afford tertiary amine-capped CDs, which are stable without any cross-linking between particles or adjacent surface groups and are, consequently, used as highly photostable and water-soluble photosensitizers in photocatalytic redox processes [40].  Surface passivation allows one to increase the durability and photostability of CDs by hindering their photocorrosion and minimizing their direct contact with pollutants or reactants. Several nonemissive polymers and organic molecules without chromophores absorbing UV, visible, or nearinfrared light are often used as passivation agents, as exemplified by poly(ethylene glycol) diamine with an average molecular weight of 1500 (PEG1500N), poly(propionylethyleneimine-co-ethyleneimine (PPEI-EI) [41], polyethyleneimine (PEI) [42], and branched polyethyleneimine (BPEI) [43]. A survey of recent research indicates that oligomeric PEG1500N, PPEI-EI, PEI, and BPEI are among the most effective cationic polymer-based passivation agents [44][45][46], allowing for one to improve fluorescent properties and photostability as well as achieve low toxicity [47]. CDs-PEG1500N, CDs-EI, and CDs-PEI have been used as non-toxic probes for in vitro fluorescent bioimaging and drug delivery in zebrafish [46,48]; however, CDs-BPEI proved to be highly toxic to fish embryos [47]. In the case of surface passivation with PEG1500N, thionyl chloride is widely used as a coupling agent for CD modification [49] ( Figure 5A). Moreover, bis(3-aminopropyl)-terminated oligomeric PEG1500N and 2,2′-(ethylenedioxy)bis(ethylamine) (EDA) were efficiently used to passivate the CD surface [50] for fluorescent cell labeling ( Figure 5B). The thus synthesized CDs-PEG1500N and CDs-EDA featured relatively high QYs and good stability over a wide pH range [51].  Surface passivation allows one to increase the durability and photostability of CDs by hindering their photocorrosion and minimizing their direct contact with pollutants or reactants.
Several non-emissive polymers and organic molecules without chromophores absorbing UV, visible, or near-infrared light are often used as passivation agents, as exemplified by poly(ethylene glycol) diamine with an average molecular weight of 1500 (PEG 1500N ), poly(propionylethyleneimine-co-ethyleneimine (PPEI-EI) [41], polyethyleneimine (PEI) [42], and branched polyethyleneimine (BPEI) [43]. A survey of recent research indicates that oligomeric PEG 1500N , PPEI-EI, PEI, and BPEI are among the most effective cationic polymer-based passivation agents [44][45][46], allowing for one to improve fluorescent properties and photostability as well as achieve low toxicity [47]. CDs-PEG 1500N , CDs-EI, and CDs-PEI have been used as non-toxic probes for in vitro fluorescent bioimaging and drug delivery in zebrafish [46,48]; however, CDs-BPEI proved to be highly toxic to fish embryos [47]. In the case of surface passivation with PEG 1500N , thionyl chloride is widely used as a coupling agent for CD modification [49] ( Figure 5A). Moreover, bis(3-aminopropyl)-terminated oligomeric PEG 1500N and 2,2 -(ethylenedioxy)bis(ethylamine) (EDA) were efficiently used to passivate the CD surface [50] for fluorescent cell labeling ( Figure 5B). The thus synthesized CDs-PEG 1500N and CDs-EDA featured relatively high QYs and good stability over a wide pH range [51].  Surface passivation allows one to increase the durability and photostability of CDs by hindering their photocorrosion and minimizing their direct contact with pollutants or reactants. Several nonemissive polymers and organic molecules without chromophores absorbing UV, visible, or nearinfrared light are often used as passivation agents, as exemplified by poly(ethylene glycol) diamine with an average molecular weight of 1500 (PEG1500N), poly(propionylethyleneimine-co-ethyleneimine (PPEI-EI) [41], polyethyleneimine (PEI) [42], and branched polyethyleneimine (BPEI) [43]. A survey of recent research indicates that oligomeric PEG1500N, PPEI-EI, PEI, and BPEI are among the most effective cationic polymer-based passivation agents [44][45][46], allowing for one to improve fluorescent properties and photostability as well as achieve low toxicity [47]. CDs-PEG1500N, CDs-EI, and CDs-PEI have been used as non-toxic probes for in vitro fluorescent bioimaging and drug delivery in zebrafish [46,48]; however, CDs-BPEI proved to be highly toxic to fish embryos [47]. In the case of surface passivation with PEG1500N, thionyl chloride is widely used as a coupling agent for CD modification [49] ( Figure 5A). Moreover, bis(3-aminopropyl)-terminated oligomeric PEG1500N and 2,2′-(ethylenedioxy)bis(ethylamine) (EDA) were efficiently used to passivate the CD surface [50] for fluorescent cell labeling ( Figure 5B). The thus synthesized CDs-PEG1500N and CDs-EDA featured relatively high QYs and good stability over a wide pH range [51].  Element doping, e.g., N-doping or dual element doping, can enhance the photocatalytic and luminescent properties of CDs. Nitrogen-doped CDs (N-CDs) exhibit improved photocatalytic activity, as the nitrogen atom has a size that is similar to that of the carbon atom and effectively binds with the latter atoms via five valence electrons [52,53]. Among the photocatalytic applications of N-CDs, one should note those that are related to water treatment and the degradation of organic acids and synthetic dyes [54,55]. N-CDs that are produced via one-pot hydrothermal treatment of cellulose in urea solution [41] exhibit blue-green fluorescence and excitation-dependent emission with QYs of up to 21%. Moreover, the presence of auxochromic nitrogen atoms within the CD architecture results in high QY and promising fluorescent properties. Another work reported the synthesis of sulfurand nitrogen-co-doped CDs (N,S-CDs), and probed their emission performance under visible-light excitation at 420-520 nm [56]. CDs, N-CDs, S-CDs, and N,S-CDs were prepared by carbonization of citric acid, ethylenediaminetetraacetic acid (EDTA), a mixture of mercaptoacetic and citric acids, and l-cysteine, respectively. Among these CDs, N,S-CDs featured the broadest visible absorption range and the highest absorption intensity in aqueous solution [56].
For CD composite-based photocatalysts, upconverted photoluminescence characteristics for the simultaneous absorption of photons with visible-to-infrared wavelengths (500-1000 nm) and strong emission in the UV-to-visible range (325-425 nm) were observed ( Figure 6A). The complexation of CDs with TiO 2 and SiO 2 semiconductors was proposed to extend absorption into the UV range, and TiO 2 /CD and SiO 2 /CD composites were produced by sol-gel methods [32]. Figure 6B shows scanning electron microscope (SEM) and HR-TEM images of as-synthesized TiO 2 /CD and SiO 2 /CD photocatalysts, revealing that CDs were attached to the surfaces of TiO 2 or SiO 2 nanoparticles. Regarding the upconverted photoluminescence characteristics of CDs, Figure 6C [58]. N-CDs were synthesized from aspartic acid and mixed with graphene oxide solution to form the aerogel composite that was used for the photocatalytic degradation of Cr(VI) under visible light. Later, a 0D/2D CD/g-C 3 N 4 composite was investigated as a photocatalyst for sulfamethazine degradation. The 0D/2D heterojunctions of CDs/g-C 3 N 4 were synthesized by homogeneous thermal pyrolysis of urea and citric acid as the precursors of g-C 3 N 4 and CDs, respectively [59]. A similar one-step homogeneous thermal pyrolysis process that was induced by melting a mixture of citric acid and urea in water was used to synthesize g-C 3 N 4 -CD photocatalysis for water splitting [60]. Graphitic CDs are commonly produced from citric acid [13,61], while urea typically acts as a crosslinking agent for the polymerization of the g-C 3 N 4 network [62,63]. The multiple absorption bands of chemically bonded N-doped CDs were attributed to the π→π* and n→π* transitions of C = C and C = O bonds [64], as well as those of conjugated aromatic C = N bonds [65]. Importantly, the produced CDs featured a good size distribution (1.6-3.0 nm), and the CDs/g-C 3 N 4 composite displayed strong photoluminescence at~540 nm with excitation wavelength-independent emission [60]. wavelengths and then relax by emitting short-wavelength UV photons to induce the photoexcitation of TiO2 and SiO2, which results in the generation of electron-hole pairs and liberation of reactive oxygen species (ROS), such as OH • and O2 •− , causing subsequent pollutant degradation. Second, CDs with a proper band gap facilitate electron transfer from the TiO2 surface after photoexcitation, thus promoting the separation of charges and enhancing the charge transfer for photocatalytic reactions at the photocatalyst surface. Thus, TiO2/CD and SiO2/CD photocatalysts facilitate the effective utilization of the full sunlight spectrum. Metal oxide-decorated CDs have been reported as promising photocatalysts. A facile two-step approach has been used to synthesize CDs that are anchored on TiO 2 nanotube arrays (TiO 2 NTAs). Electrochemical anodization was performed to prepare TiO 2 NTAs, and CDs that were produced by electrolysis of graphite rods were subsequently anchored by electrochemical deposition. The synthesized CDs/TiO 2 NTAs acted as a sensitizer to extend the range of light absorption toward the full solar spectrum and, thus, enhance the photocatalytic degradation of pollutants and the efficiency of H 2 production via water splitting [66]. CDs that were anchored on an octahedral CoO under hydrothermal conditions also exhibited outstanding performance for photocatalytic water splitting [67]. Moreover, CDs could be fabricated by electrochemical etching of graphite rods, and CD-Fe 2 O 3 nanocomposites that were constructed by facile heat treatment in a tube furnace were found to efficiently catalyze the overall water splitting under visible light in the absence of any external biases or scavengers [68].
The use of composites of transition metal dichalcogenide and CDs in photocatalysis remains underexplored. Zhao et al. [69] hydrothermally synthesized a CDs/MoS 2 composite as a catalyst for the hydrogen evolution reaction. CDs that were prepared by electrochemical etching were mixed with MoS 2 precursors (Na 2 MoO 4 and l-cysteine) under hydrothermal conditions, and centrifugation then isolated the solid precipitate of CDs/MoS 2 containing thin nanosheets (lateral dimension = 50-100 nm). CDs/MoS 2 exhibited good catalytic activity for the hydrogen evolution reaction with high cathodic current density and a positive onset over-potential of~0.109 V. Surprisingly, even better performance was observed when the CD/MoS 2 catalyst was exposed to visible light for 30 min. Recently, hybrid CDs/tungsten disulfide quantum dots (CDs/WS 2 QDs) have been prepared from sodium tungstate dihydrate and l-cysteine by a bottom-up hydrothermal method and were used as a luminescent probe for the detection of H 2 O 2 and the enzymatic sensing of glucose [70].
Moreover, CDs/WS 2 nanorods were found to be suitable for microscopic cell imaging and photothermal therapy. NH 2 -functionalized WS 2 nanorods were mixed with glucose surfactant suspension, followed by thermal treatment to give carbonization CDs that were covalently bound to the WS 2 nanorods [71]. Notably, the CDs/WS 2 nanorods featured excitation-dependent photoluminescence with a maximum at 430 nm (cf. 450 nm for CDs), which was ascribed to the covalent conjugation of CDs and WS 2 nanorods. Similar photoluminescence phenomena were observed for the covalent binding of CDs with other molecules [72].
The photocatalytic applications of CDs have been investigated in a variety of fields, including water treatment, chemical degradation, water splitting, hydrogen evolution, and bio-related applications. The experimental and mechanistic studies on the photocatalytic role of CDs are discussed below.

Water Treatment and Chemical Degradation
CDs play an important role in photocatalytic water treatment and chemical degradation. During photocatalytic process, electrons (e − ) in the photocatalyst are excited by the photon energy and they are promoted from the valence band (VB) to the conduction band (CB). At the same time, the holes (h + ) generated in the VB migrates to the surface of photocatalysts, specifically, to the attached CDs as an acceptor of photogenerated holes to prevent electron-hole recombination during photocatalytic processes [29]. Li et al. [32] investigated the photoreduction of methylene blue under visible light that is catalyzed by CD-and nanoparticle-based materials, such as SiO 2 /CDs, TiO 2 /CDs, SiO 2 nanoparticles, TiO 2 nanoparticles, and CDs. The complete degradation of methylene blue was achieved in the presence of SiO 2 /CDs and TiO 2 /CDs, while SiO 2 nanoparticles, TiO 2 nanoparticles, and CDs had no effect on methylene blue degradation. Therefore, CDs were concluded to be essential for visible-light photodegradation, as pure SiO 2 and TiO 2 were completely inactive. Figure 6C explains the mechanistic role of CDs in photodegradation [32]. When the TiO 2 /CDs or SiO 2 /CDs photocatalyst is photoilluminated, the CDs absorb visible light, and then emit shorter wavelength light (325 to 425 nm), which in turn excites TiO 2 or SiO 2 to form electron/hole (e − /h + ) pairs. The electron/hole pairs then react with the adsorbed oxidants/reducers (usually O 2 /OH − ) to produce active oxygen radicals (e.g., ·O 2 − , ·OH), which subsequently cause the degradation of the methylene blue dyes, as illustrated in Figure 6D [57]. Promising photocatalytic activity for rhodamine B degradation was achieved by sulfur and nitrogen co-doped CDs(N,S-CDs)/TiO 2 composites under excitation at 420-520 nm [54]. N,S-CDs also achieved the rapid mineralization of nitrophenols under visible light [56]. A CD model consisting of 42 carbon atoms, 18 hydrogen atoms, and 1 oxygen atom (C 42 H 18 O) was used to study the electronic structure of the undoped CDs. The doping of CDs with one sulfur atom (C 40 H 16 OS) decreased the band gap from 3.440 to 3.247 eV, while doping with two nitrogen atoms (C 39 H 16 ON 2 ) decreased the band gap to 3.234 eV. Interestingly, the band gap of N,S-CDs was further reduced to 3.103 eV, which indicates that nitrogen and sulfur co-doping was most effective in reducing the band gap, mainly because heteroatom doping results in the charge redistribution of doped CDs [73]. The achieved Cr(VI) degradation efficiency (90.6%) exceeded those that were obtained for CD/GA composite without N-doping and N-CDs without the graphene aerogel when visible light (λ > 420 nm)-driven water remediation was catalyzed by 3D N-CD/graphene aerogel (N-CD/GA) composites [57]. During the catalytic degradation of Cr(VI), potassium dichromate (K 2 Cr 2 O 7 ) was used as a model compound and, due to the presence of triethanolamine as a sacrificial agent, CrO 4 2− anion is the main chemical form of Cr (VI) in alkaline solutions. The photocatalytic reduction of Cr(VI) can be expressed as CrO 4 2− + 8H + + 3e − = Cr 3+ + 4H 2 O. Under visible-light irradiation, the electrons in the HOMO of N-CDs are excited to the LUMO, which leaves the former orbital with holes that can oxidize triethanolamine as an electron donor. The photogenerated electrons on N-CDs migrate to the surface of the graphene aerogel and then reduce toxic Cr(VI) to nontoxic Cr(III). Despite its promising photophysical and electronic properties, graphitic carbon nitride (g-C 3 N 4 ) only exhibits moderate photocatalytic performance [74,75]. Most recently, a 0D/2D CD/g-C 3 N 4 composite has been investigated in terms of photocatalytic activity for the degradation of sulfamethazine (SMZ) under irradiation with LED light (380-780 nm) [59]. CDs/g-C 3 N 4 (CDCNs) were denoted as CDCN-n, where n is the initial mass of citric acid as a precursor for the synthesis of CDs [59]. CDCN-10 presented the highest photocatalytic performance, achieving an approximately 90% degradation under irradiation with LED (420-500 nm) light or Xe lamp (380-780 nm). Specifically, to completely degrade SMZ, the energy consumption of LED (ca. 50 Wh) was estimated to be ca. 15 times less than that of Xe lamp (ca. 750 Wh). Therefore, LED was more effective than Xe lamps in terms of decomposing SMZ and energy consumption. The Mott-Schottky plots were applied and considered as the conduction-band energy (ECB) to further clarify the effects of CDs on the band structure of CDs/g-C 3 N 4 . Figure 7A shows that the conduction-band energy from the Mott-Schottky plots of g-C 3 N 4 and CDCN-10 at −1.42 and −1.28 eV, respectively. Moreover, electrochemical impedance spectroscopy was used to elucidate the photosemiconductor charge generation, migration, and separation behaviors, and the curvature radius of the corresponding Nyquist plot was indicative of electron transfer resistance [76]. The results revealed that the charge transfer resistance of g-C 3 N 4 substantially exceeded that of CDs/g-C 3 N 4 ( Figure 7B), which implied that CDs accelerated charge transfer during photocatalysis. The generated electrons also partially reacted with dissolved oxygen to form O 2 •− , as the standard redox potential of is less negative than the conduction-band potential of CDs/g-C 3 N 4 (−1.28 eV). Other ROS, such as OH • , 1 O 2 , and H 2 O 2 , could also be generated to assist the degradation of sulfamethazine due to the O 2 •− transformation [59] ( Figure 7C).
impedance spectroscopy was used to elucidate the photosemiconductor charge generation, migration, and separation behaviors, and the curvature radius of the corresponding Nyquist plot was indicative of electron transfer resistance [76]. The results revealed that the charge transfer resistance of g-C3N4 substantially exceeded that of CDs/g-C3N4 ( Figure 7B), which implied that CDs accelerated charge transfer during photocatalysis. The generated electrons also partially reacted with dissolved oxygen to form O2 •− , as the standard redox potential of O2/O2 •− (−0.33 eV) is less negative than the conduction-band potential of CDs/g-C3N4 (−1.28 eV). Other ROS, such as OH • , 1 O2, and H2O2, could also be generated to assist the degradation of sulfamethazine due to the O2 •− transformation [59] ( Figure 7C). Most recently, a study revealed the effect of precursors and synthesis methods on CDs characteristics and their photoinduced electron transfer (PET) reactivity for single electron photoreduction of methyl viologen MV 2+ (−0.45 V vs. NHE) to its mono-reduced species (MV •+ ). The synthesis of CDs from all glucose, fructose, and citric acid using hydrothermal synthesis yielded low density and amorphous CDs, while that using pyrolysis rendered graphitic structures. Citric acidderived CDs were the most photoactive nano-systems, followed by fructose and glucose analogues. Graphitic CDs from citric acid and glucose facilitated higher performance on photoreduction of MV 2+ when compared with amorphous CDs. However, the contradict results of amorphous CDs were found for fructose precursor. The reason for this inversion was possibly due to the formation of the supramolecular aggregates from large graphitic materials, which affects the PET efficiency [77]. Another work additionally disclosed that the hydrothermal syntheses yielded amorphous CDs from citric acid, which were either nondoped (a-CDs) or nitrogen-doped (a-N-CDs), whereas the pyrolytic treatment afforded graphitic CDs, either non-doped (g-CDs) or nitrogen-doped (g-N-CDs) [78]. For non-nitrogen-doped CDs, graphitic CDs works utmost in the photoreduction of MV 2+ relative to amorphous CDs, nevertheless amorphous nitrogen-doped CDs are greater active when compared to their graphitic N-CDs.  Most recently, a study revealed the effect of precursors and synthesis methods on CDs characteristics and their photoinduced electron transfer (PET) reactivity for single electron photoreduction of methyl viologen MV 2+ (−0.45 V vs. NHE) to its mono-reduced species (MV •+ ). The synthesis of CDs from all glucose, fructose, and citric acid using hydrothermal synthesis yielded low density and amorphous CDs, while that using pyrolysis rendered graphitic structures. Citric acid-derived CDs were the most photoactive nano-systems, followed by fructose and glucose analogues. Graphitic CDs from citric acid and glucose facilitated higher performance on photoreduction of MV 2+ when compared with amorphous CDs. However, the contradict results of amorphous CDs were found for fructose precursor. The reason for this inversion was possibly due to the formation of the supramolecular aggregates from large graphitic materials, which affects the PET efficiency [77]. Another work additionally disclosed that the hydrothermal syntheses yielded amorphous CDs from citric acid, which were either nondoped (a-CDs) or nitrogen-doped (a-N-CDs), whereas the pyrolytic treatment afforded graphitic CDs, either non-doped (g-CDs) or nitrogen-doped (g-N-CDs) [78]. For non-nitrogen-doped CDs, graphitic CDs works utmost in the photoreduction of MV 2+ relative to amorphous CDs, nevertheless amorphous nitrogen-doped CDs are greater active when compared to their graphitic N-CDs.
Briefly, CDs can significantly improve the efficiency of photocatalytic water treatment and chemical degradation in view of their upconversion properties and the promotional effect on charge transfer to suppress electron-hole recombination. However, the role of surface chemistry of CDs in the induction of charge photogeneration needs to be further clarified.

Water Splitting and Hydrogen Evolution
Hydrogen production by solar-energy-driven water splitting has been extensively studied as a means of green mass production of hydrogen to cover future energy demand. During photocatalytic water splitting, water is decomposed into hydrogen and oxygen according to eq. (1) (Figure 8). Wang et al. [81] designed a hybrid photocatalyst containing inner CDs that were attached to outer layer of single-layer carbon nitride (C3N) to control the reduction and oxidation sites during water splitting. C3N is a graphene-like planar hexagonal structure with the nitrogen being uniformly distributed. The geometric and electronic structures of C3N were studied with density functional theory (DFT) prior to combination with CDs. The simulations suggested that this hybrid material can harvest the entire visible and infrared light for water splitting. Upon irradiation with visible light, Recent reviews have summarized the influence of CDs on the efficiency of photocatalytic water splitting for hydrogen production [79,80]. A recent work on the role of graphitic CDs that are anchored on TiO 2 nanotube arrays (TiO 2 NTAs) in photocatalytic water splitting [66] showed that CDs in CDs/TiO 2 NTAs act as a sensitizer for extending the light absorption range toward the full solar spectrum. Electrochemical impedance spectroscopy was used to analyze electron-hole pair separation and transfer under light irradiation, revealing that CDs strongly reduced charge transfer resistance. Photoelectrochemical tests that were performed at various deposition times showed that the photoelectron density generated by CDs/TiO 2 NTAs exceeded that generated by pristine TiO 2 NTAs. The former composite additionally featured an extended absorption spectrum spanning both visible and near-infrared (NIR) ranges [66]. Optimal photocatalytic water splitting under visible-light irradiation (λ > 400 nm) was achieved while using a CD/CoO composite as a photocatalyst, with the observed hydrogen and oxygen evolution rates (1.67 and 0.91 µmol h −1 , respectively) corresponding to the expected 2:1 stoichiometry. These production rates were up to six-fold higher than those of pristine CoO. The photogenerated electrons in the conduction band of CoO spontaneously migrated to CDs for hydrogen evolution, owing to the effect of CDs on electron transfer, as illustrated in Figure 8A. This migration suppressed the recombination of electron-hole pairs and, thus, increased the photocatalytic activity of CoO. In addition, CDs can act as a heat conductor for dissipating the heat accumulated because of the photothermal effect at the surface of CoO and, thus, prevent its deactivation [67]. The CDs/Fe 2 O 3 composite can be also used for a water splitting catalyst. CDs were found to decrease the separation between the hematite (Fe 2 O 3 ) conduction band and H + /H 2 potential. The ionization potential that was equivalent to the valence band energy (E V ) of CDs/Fe 2 O 3 was measured by ultraviolet photoelectron spectroscopy (UPS). The E V value is determined to be 6.29 eV by subtracting the width of the He I UPS spectrum from the exciting energy (21.22 eV). The Ev value from UPS measurement is consistent with that from electrochemistry while using cyclic voltammetry of CDs/Fe 2 O 3 , which can be used to investigate the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of CDs/Fe 2 O 3 using the ferrocene redox system as the external standard. E HOMO and E LUMO were calculated from E HOMO = −(Eox onset − E ferrocene + 4.8) eV and E LUMO = −(E red onset − E ferrocene + 4.8) eV, respectively, where E ox onset , E red onset , and E ferrocene are the onset of oxidation and reduction potential of CDs/Fe 2 O 3 and the oxidation potential of ferrocene, respectively. The calculated HOMO/LUMO energy levels are −6.255/−4.233 eV for CDs/Fe 2 O 3 corresponding to the bandgap of 2.02 eV for CDs/Fe 2 O 3 , while the bandgap of Fe 2 O 3 was reported to be 2.1 eV [68]. CDs/Fe 2 O 3 nanocomposites with 5 wt% CDs effectively promoted photocatalytic water splitting under visible-light irradiation in the absence of scavengers or external bias, affording hydrogen and oxygen at rates of 0.390 and 0.225 µmol h −1 , respectively. Figure 8B illustrates the visible-light absorption of Fe 2 O 3 (λ ≥ 420 nm) and the generation of electron-hole pairs upon visible-light irradiation. The holes directly reacted with water to produce O 2 , while the photogenerated electrons were transferred from the conduction band of Fe 2 O 3 to CDs for hydrogen evolution. Finally, CDs additionally improved the light absorption of Fe 2 O 3 and enhanced the charge separation ability, as evidenced by the reduced resistance [68] (Figure 8C).
Wang et al. [81] designed a hybrid photocatalyst containing inner CDs that were attached to outer layer of single-layer carbon nitride (C 3 N) to control the reduction and oxidation sites during water splitting. C 3 N is a graphene-like planar hexagonal structure with the nitrogen being uniformly distributed. The geometric and electronic structures of C 3 N were studied with density functional theory (DFT) prior to combination with CDs. The simulations suggested that this hybrid material can harvest the entire visible and infrared light for water splitting. Upon irradiation with visible light, free electrons and holes are formed in the hybrid CD-C 3 N composite, with electrons accumulating in the inner CDs and the holes accumulating on the outer C 3 N layer. Holes at the C 3 N oxidation sites attack the adsorbed water molecules and promote their splitting to generate protons, which penetrate C 3 N due to the low barrier of 2.30 eV based on the concentration gradient and electrostatic attraction. In contrast, oxygen-containing products cannot penetrate the above layer because of the high penetration barrier of 6.28 eV. After migration, protons combine with electrons on CD reduction sites to generate H 2 . As only protons and H atoms penetrate C 3 N, the produced H 2 is stored in the C 3 N layer and separated from oxygen species [81]. Thus, the above hybrid is a promising material for photocatalytic water splitting.
The difficulty of overall water splitting for hydrogen and oxygen production lies in the control of the reduction and oxidation sites, which should be located within a close distance in the same photocatalyst. Therefore, the reverse reaction and even explosion can occur when the hydrogen and oxygen that are produced in/on a photocatalyst are combined. Metal-free hybrid materials are attractive photocatalysts for the practical conversion of solar energy and the generation/utilization of hydrogen in view of their well-separated reduction-oxidation characteristics. However, experimental evidence is needed to confirm the theoretical assumption that is based on molecular simulations.

Enzyme-Mimetic and Photodynamic Applications
CDs exhibit outstanding electrochemiluminescent properties, similar to semiconductor QDs, which, together with their high biocompatibility, low toxicity, easy synthesis, high chemical inertness, excitation-dependent multicolor emission, and photobleaching resistance, make CDs attractive for bio-related applications. Herein, we focus on the nanozyme and photodynamic applications of CDs.
Natural photosynthesis has inspired the use of synthetic enzymes in photocatalysis. In particular, the remarkable water dispersibility of CDs, attributed to their abundant hydrophilic groups introduced by surface engineering, makes them promising nanomaterials for nanozyme applications. Recent research has uncovered the important role of peroxidases (POD) as drivers of angiogenesis, which is related to tumor growth [82]. CDs were shown to exhibit POD-like activity in the presence of H 2 O 2 , as evaluated by the color of oxidized chromogenic substrates [83], e.g., o-phenylenediamine (OPD), hydroquinone, 1,2,3-trihydroxybenzene (THB), and 3,3 ,5,5 -tetramethylbenzidine (TMB). Among them, TMB is the most widely used substrate for investigating POD-and horseradish peroxidase (HRP)-mimetic activity of nanozymes due to its low carcinogenicity and strong absorbance [84][85][86]. Shi et al. [87] discovered that candle soot-derived CDs exhibit POD-like catalytic activity for THB, OPD, and TMB oxidation in the presence of H 2 O 2 . The developed color indicates the quantity of oxidized TMB, as illustrated in Figure 9. In contrast to HRP, CDs exhibit very stable catalytic activity over a broad temperature range (0-90 • C) and a wide pH range (pH 2-12). Moreover, the catalytic mechanism of CDs, which is based on a ping-pong model, is similar to that of HRP, with CDs having a higher affinity to POD substrates and H 2 O 2 [87]. The combination of POD-mimetic CDs with glucose oxidase (GOx) was shown to provide a cheap, simple, selective, and sensitive assay for colorimetric glucose sensing in serum [87].
Catalysts 2020, 10, x FOR PEER REVIEW 15 of 22 hydrogen in view of their well-separated reduction-oxidation characteristics. However, experimental evidence is needed to confirm the theoretical assumption that is based on molecular simulations.

Enzyme-Mimetic and Photodynamic Applications
CDs exhibit outstanding electrochemiluminescent properties, similar to semiconductor QDs, which, together with their high biocompatibility, low toxicity, easy synthesis, high chemical inertness, excitation-dependent multicolor emission, and photobleaching resistance, make CDs attractive for bio-related applications. Herein, we focus on the nanozyme and photodynamic applications of CDs.
Natural photosynthesis has inspired the use of synthetic enzymes in photocatalysis. In particular, the remarkable water dispersibility of CDs, attributed to their abundant hydrophilic groups introduced by surface engineering, makes them promising nanomaterials for nanozyme applications. Recent research has uncovered the important role of peroxidases (POD) as drivers of angiogenesis, which is related to tumor growth [82]. CDs were shown to exhibit POD-like activity in the presence of H2O2, as evaluated by the color of oxidized chromogenic substrates [83], e.g., ophenylenediamine (OPD), hydroquinone, 1,2,3-trihydroxybenzene (THB), and 3,3′,5,5′tetramethylbenzidine (TMB). Among them, TMB is the most widely used substrate for investigating POD-and horseradish peroxidase (HRP)-mimetic activity of nanozymes due to its low carcinogenicity and strong absorbance [84][85][86]. Shi et al. [87] discovered that candle soot-derived CDs exhibit POD-like catalytic activity for THB, OPD, and TMB oxidation in the presence of H2O2. The developed color indicates the quantity of oxidized TMB, as illustrated in Figure 9. In contrast to HRP, CDs exhibit very stable catalytic activity over a broad temperature range (0-90 °C) and a wide pH range (pH 2-12). Moreover, the catalytic mechanism of CDs, which is based on a ping-pong model, is similar to that of HRP, with CDs having a higher affinity to POD substrates and H2O2 [87]. The combination of POD-mimetic CDs with glucose oxidase (GOx) was shown to provide a cheap, simple, selective, and sensitive assay for colorimetric glucose sensing in serum [87]. Recent years have witnessed significant progress in the application of CDs as photosensitizers and photodriven nanozymes [40,88,89]. Hutton et al. [40] reported light-driven enzymatic catalysis by CDs for a system of simultaneous hydrogenation and hydrogen production. Positively charged ammonium-doped CDs (CD-NHMe2 + ) allowed for the photoexcited electrons to be transferred to negatively charged fumarate reductase (FccA) for the reduction of fumarate to succinate via hydrogenation with a turnover number of 6,000 mol succinate per mol FccA within 24 h, as demonstrated for system A in Figure 10A. Simultaneously, CD-NHMe2 + could enhance solar Recent years have witnessed significant progress in the application of CDs as photosensitizers and photodriven nanozymes [40,88,89]. Hutton et al. [40] reported light-driven enzymatic catalysis by CDs for a system of simultaneous hydrogenation and hydrogen production. Positively charged ammonium-doped CDs (CD-NHMe 2 + ) allowed for the photoexcited electrons to be transferred to negatively charged fumarate reductase (FccA) for the reduction of fumarate to succinate via hydrogenation with a turnover number of 6,000 mol succinate per mol FccA within 24 h, as demonstrated for system A in Figure 10A. Simultaneously, CD-NHMe 2 + could enhance solar hydrogen generation by transferring photogenerated electrons to [NiFeSe]-hydrogenase (H 2 ase) for hydrogen production via proton reduction with turnover numbers of 43,000 mol H 2 per mol H 2 ase in 24 h, as demonstrated for system B in Figure 10A. In contrast, negatively charged CDs with carboxyl groups (CD-COO − ) exhibited little or no effect on both of the reactions [40]. Lin et al. [88] designed a CD-based dual optical and photoelectrochemical immunosensing system for monitoring aflatoxin B1 (AFB 1 ) in food, which achieved highly selective AFB 1 detection in a magneto-controlled immunoreaction system ( Figure 10B). GOx delivered on the tag oxidized glucose to gluconic acid and H 2 O 2 once the immunocomplexes of GOx-labeled bovine serum albumin-AFB 1 were formed. Subsequently, MnO 2 nanosheets on the MnO 2 -CD-coated electrode reacted with H 2 O 2 to induce the dissociation of CDs and photocurrent decline. The detection of AFB 1 was achieved in the range of 0.01-20 ng mL −1 , with a detection limit of 2.1 pg mL −1 (ppt) [88]. The established immunoassay demonstrated satisfactory accuracy and good reproducibility. Zhang et al. [89] used phosphorescent CDs as a photo-oxidative nanozyme for antimicrobial photodynamic inactivation, achieving 92 and 86% growth inhibition efficiencies against Escherichia coli and Salmonella under light irradiation, respectively. In contrast, phloxine B, which is a commercial photosensitizer, displayed inhibition efficiencies of only 40 and 55%, respectively. Figure 10C(a) illustrates the photodriven activation of oxygen on the photosensitizer to produce singlet oxygen from triplet O 2 , which is the cheapest, most abundant, and environmentally friendly oxidant. Promising photosensitizers facilitate the transition of fluorescence to phosphorescence with a high yield of the triple state, and the photosensitization efficiency is proportional to phosphorescence ( Figure 10C(b)). CDs exhibited the activity of an oxidase-mimicking nanozyme, as confirmed by the strong absorbance at~652 nm, due to the photo-oxidation of TMB ( Figure 10C(c)). Similarly, a CD/polydimethylsiloxane composite was reported to exhibit photodynamic antibacterial activity against E. coli, Staphylococcus aureus, and Klebsiella pneumonia under blue-light irradiation for only 15 min. [90].
Catalysts 2020, 10, x FOR PEER REVIEW 16 of 22 CD-based dual optical and photoelectrochemical immunosensing system for monitoring aflatoxin B1 (AFB1) in food, which achieved highly selective AFB1 detection in a magneto-controlled immunoreaction system ( Figure 10B). GOx delivered on the tag oxidized glucose to gluconic acid and H2O2 once the immunocomplexes of GOx-labeled bovine serum albumin-AFB1 were formed. Subsequently, MnO2 nanosheets on the MnO2-CD-coated electrode reacted with H2O2 to induce the dissociation of CDs and photocurrent decline. The detection of AFB1 was achieved in the range of 0.01-20 ng mL −1 , with a detection limit of 2.1 pg mL −1 (ppt) [88]. The established immunoassay demonstrated satisfactory accuracy and good reproducibility. Zhang et al. [89] used phosphorescent CDs as a photo-oxidative nanozyme for antimicrobial photodynamic inactivation, achieving 92 and 86% growth inhibition efficiencies against Escherichia coli and Salmonella under light irradiation, respectively. In contrast, phloxine B, which is a commercial photosensitizer, displayed inhibition efficiencies of only 40 and 55%, respectively. Figure 10C(a) illustrates the photodriven activation of oxygen on the photosensitizer to produce singlet oxygen from triplet O2, which is the cheapest, most abundant, and environmentally friendly oxidant. Promising photosensitizers facilitate the transition of fluorescence to phosphorescence with a high yield of the triple state, and the photosensitization efficiency is proportional to phosphorescence ( Figure 10C(b)). CDs exhibited the activity of an oxidase-mimicking nanozyme, as confirmed by the strong absorbance at ~652 nm, due to the photooxidation of TMB ( Figure 10C(c)). Similarly, a CD/polydimethylsiloxane composite was reported to exhibit photodynamic antibacterial activity against E. coli, Staphylococcus aureus, and Klebsiella pneumonia under blue-light irradiation for only 15 min. [90]. To sum up, the photoresponsive characteristics and efficient endorsement of redox enzyme activity of CDs allow for them to be used in numerous enzyme-driven reactions (e.g., hydrogenation and hydrogen evolution). Moreover, the exceptional photosensitization behavior of CDs for singlet oxygen generation can be used in photodynamic therapy, which broadens the research scope for CD utilization in photobiocatalysis. Nevertheless, to more precisely realize controllable reactions, one To sum up, the photoresponsive characteristics and efficient endorsement of redox enzyme activity of CDs allow for them to be used in numerous enzyme-driven reactions (e.g., hydrogenation and hydrogen evolution). Moreover, the exceptional photosensitization behavior of CDs for singlet oxygen generation can be used in photodynamic therapy, which broadens the research scope for CD utilization in photobiocatalysis. Nevertheless, to more precisely realize controllable reactions, one should further investigate suitable chemical modifications of the CD surface, allowing for resistance toward photodegradation and increased stability during photodriven reactions.

Summary and Future Prospects
CD research, development, and applications have recently drawn significant attention. The ability of functionalized CDs to absorb in the entire solar spectrum range, from ultraviolet to NIR, makes them outstanding materials for multi-disciplinary research in the fields of photocatalysis, photoelectrocatalysis, and optoelectronics. Photoluminescence is another fascinating optical feature of CDs regarding their emission ability due to their tunable, photoresponsive characteristics. Besides, the upconverted photoluminescent behavior of CDs, which can efficiently absorb at multiple wavelengths and emit relatively short-wavelength light, potentially expands their benefits to the advanced progress of fabricating various remarkable photodevices. When combined with low toxicity and biocompatibility, the photoresponsive behavior of CDs expands their application scope to the area of bio-related research, including enzyme-mimetic and photodynamic applications. However, we do not deal with other bio-applications, such as biosensing, bioimaging, and phototheranostics, in this review because they are not related to catalysis.
Currently, the main challenges of CD research and development are the limited potential for commercialization and the determination of the most suitable modification for target applications. Conventionally, top-down methods of CDs synthesis, such as laser ablation, ultrasonication, and electrochemical etching of graphite or carbon materials, have been used. Recently, scalable bottom-up methods of CD synthesis from carbon-containing molecules, including carbohydrates, organic acids, and natural products, have been developed to accurately control CD morphology and size for large-scale production. Moreover, in the case of bottom-up approaches, the synthesis and surface modification of CDs can be performed in a single step. Most CD synthesis techniques feature hydrothermal treatment, chemical treatment, microwave synthesis, solvothermal treatment, and plasma treatment, and are, therefore, challenging to integrate with the thermochemical conversion of biomass to fuels and bio-crudes, which are carbon-rich materials.
To obtain CDs with tunable and distinctive optical and photoluminescent characteristics, one should control their size and surface modification. After synthesis, downstream processing and purification of CDs are crucial, as the low density and surface charge of CDs make them difficult to separate by normal centrifugation. Most of the researchers applied dialysis and gel chromatography techniques to isolate CDs with a particular size. Recent works have additionally paid attention to the surface modification of CDs by functionalization with amine, carboxyl, hydroxyl, and carbonyl groups or specific molecules, passivation with polymers or organic molecules, non-metal or metal doping, and composite formation with one-dimensional/two-dimensional (1D/2D) materials.
In the case of photocatalytic applications, pure CDs cannot be used as photocatalysts or photosensitizers. However, CD composites with other photocatalysts or semiconductors can absorb photons with energy that is equal to or greater than the band gap. CDs can enhance the photocatalytic activity of these materials in two ways. First, CDs absorb long-wavelength visible light and then relax by emitting photons in the short-wavelength UV range to photoexcite semiconductor photocatalysts. Second, CDs with a proper band gap further assist photogenerated electron transfer from the surface of semiconductor photocatalysts after photoexcitation, which promotes the separation of charges and enhances charge migration efficiency by increasing the number of charge carriers that are available for photocatalytic reactions. In view of the upconverted photoluminescent properties of CDs, composites of CDs with other photocatalysts/semiconductors facilitate the effective exploitation of the whole sunlight spectrum. Consequently, the applications of CDs for light-induced catalysis, including energy conversion and storage, water splitting, hydrogen evolution, water treatment, chemical degradation, and their bio-related applications have significantly expanded in recent years. In particular, the surface modification of bio-derived CDs for enzyme-mimetic reactions, bioimaging, targeted drug delivery, and phototheranostics is a promising trend for CD applications. The surface modification of CDs to attain high solubility in aqueous media and good photostability affords versatile photosensitizers for promoting redox enzyme activity, which additionally broadens the research scope for CD utilization in photobiocatalysis.