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Catalysts 2013, 3(3), 625-645; doi:10.3390/catal3030625
Published: 31 July 2013
Abstract: The Ag-nanoparticles (Ag-NP)/TiO2 composite thin films with various amounts of Ag (10 mol% ≤ n ≤ 80 mol%) were examined as a potential photocatalyst by decoloration reaction of methylene blue (MB) in an aqueous solution. These composite thin films of ca. 100 nm thickness were fabricated by the MPM at 600 °C in air. The decoloration rates monitored by the absorption intensity of the MB solution indicated that the composite thin films of Ag with an amount less than 40 mol% are not effective under vis-irradiation, though they can work as a photocatalyst under UV-irradiation. Further, the UV-sensitivity of the composite thin films gradually decreased to almost half the level of that of the TiO2 thin film fabricated under the identical conditions when the Ag amount increased from 10 to 40 mol%. Contrarily, the composite thin films of Ag content larger than 50 mol% showed the vis-responsive activity, whose level was slightly lower than the decreased UV-sensitivity. Diffuse reflectance spectra suggested that the vis-responsive activity of the composite thin films is due to the conductivity, localized surface plasmon resonance and surface plasmon resonance of Ag-NP. It was also elucidated that the vis-responsive level of the composite thin films corresponds to their electrical conductivity that depends on the Ag content.
Metal oxide photocatalytic degradation of organic pollutants has attracted significant attention by researchers because of its usefulness in tackling environmental contaminants . Whereas titanium dioxide as a metal oxide seems to be one of the most promising semiconductors for many photocatalytic applications due to its low cost, chemical stability and non-toxicity. Its utilization remains typically confined to UV light because of its wide band gap (3.2 eV for anatase and 3.0 eV for rutile) . This limits the efficient utilization of solar energy for TiO2 because TiO2 cannot efficiently utilize solar light since UV light accounts for only 4–6% of solar radiation. Therefore, many attempts have been undertaken in recent decades to shift the threshold of the photo-response of TiO2 into the visible region, which would enhance its potential for chemical solar energy conversion and open possibilities for further applications [3,4,5,6,7].
One of the alternative approaches for achieving the threshold of the photo-response of TiO2 into the visible region is to make a composite semiconductor by modifying TiO2 with noble metals. These noble metals act separately or simultaneously depending on the photoreaction conditions, experimental methods used and they may (i) enhance the electron-hole separation by acting as electron traps [8,9,10,11], (ii) extend the light absorption into the visible range and enhance surface electron excitation by size- and shape-dependent plasmon resonances excited by visible light [7,12,13,14] and/or (iii) modify the surface properties of TiO2 [15,16]. The early methods [17,18,19], to produce noble-metal nanoparticles are still used today and continue to be the standard by which other synthesis methods are compared [20,21,22]. In particular, silver as a noble metal has attracted considerable attention, as a result of its remarkable role in the improvement of the photo-activity of semiconductors [9,13,23]. They could be reused, and handled more easily and economically if impregnated on substrates. Therefore, many researchers have focused on modifying TiO2 with Ag by synthesis Ag/TiO2 heterostructures [8,9,10,11,12,13,14,23,24].
Although the synthesis of Ag/TiO2 heterostructures was intensively reported in large quantities [8,9,10,11,12,13,14,23,24], there are few reports about Ag/TiO2 composite thin films with amounts of Ag > 18 mol%, prepared by chemical methods such as sol-gel, so far in the literatures. It is well reported that incorporating larger amount of Ag particles was limited by the sol-gel dip-coating method of up to 18 mol% due to Ag particles coalescing with each other into huge particles during sintering . Moreover, Ag/TiO2 electrodes were short-lived because Ag NPs on TiO2 are easily oxidized and dissolved in an electrolytic solution under vis-light irradiation [26,27]. Ag NPs must be coated with a SiO2 shell or Al2O3 mask to prevent foremost their oxidation by TiO2 [26,27]. By incorporating silver ions and Cu ions into clay minerals/TiO2 mixtures with different ratio, it obtained composites capable of degrading ethanol in the visible wavelength range about twice as fast as the reference photocatalyst type P25 [28,29]. Using molecular precursor method (MPM), a coating precursor solution can be prepared by a reaction of Ti(OiPr)4 with ethylenediamine-N,N,N′,N'-tetraacetic acid (EDTA) under the presence of dibutylamine and hydrogen peroxide [30,31,32]. Consecutively, the Ag acetate ethanol solution can be easily prepared, simply by dissolving the silver salt in ethanol [32,33]. The two precursor solutions can be then mixed at different molar concentration to form a composite solution [32,33]. By spin coating the composite precursor solution on quartz glass substrates, the potential of producing metallic Ag-nanoparticles/titania (Ag NP/TiO2) composite thin films with various and unprecedentedly high Ag particles, up to 80 mol% of Ag homogeneously distributed in a titania matrix can be fabricated by heat treated at 600 °C [32,33]. It was concluded that the MPM offers excellent miscibility of the silver and titania precursor solutions, and is effective for overcoming the limitations in miscibility of the conventional sol-gel method and is necessary for fabricating Ag/TiO2 composite thin films with amounts of Ag ≤ 80 mol% .
In this study, we report the photocatalytic activity of Ag-NP/TiO2 composite thin films with various amounts of Ag (10≤ Ag mol% ≤ 80) in titania and compare them with pure TiO2 thin film, both fabricated by the MPM. The relationship between the unprecedentedly high amounts of metallic silver in TiO2 and photocatalytic decoloration rate of methylene blue was examined. Homogeneous distribution and growth of Ag-NP in the composite thin films were clarified by the FE-SEM and TEM observations. The absorption spectra of Ag-NP/TiO2 composite thin films were analyzed by using Kubelk-Munk equation for diffuse reflectance spectra (DRS), in order to study the plasmonic effect of Ag-nanoparticles (Ag NP) in dielectric TiO2 matrix. The findings demonstrated that a positive relationship exists between Ag NP surface plasmon absorption and the rate enhancements of decoloration and prove the hypothesis that the metallic plasmonic enhances rates of photocatalytic reactions .
The TiO2 thin film and eight Ag-NP/TiO2 composite thin films (COMP-Agn; n = 10, 20, 30, 40, 50, 60, 70, and 80) were fabricated. The XRD and electrical conductivity results of these Ag-NP/TiO2 composite thin films are presented in our recent paper [32,33].
2.1. Chemical Characterization of Thin Films by XPS
Figure 1 shows the XPS high resolution wide scans for COMP-Ag70. The major XPS peaks include Ag 3d, Ti 2p, and O 1s. The XPS peak for C1s (284.8 eV) is due to the adventitious hydrocarbon from the XPS instrument itself. The depth profile for COMP-Ag40, 50 and 70 were scanned as shown in Figure 2; including the spectra obtained after performing Gaussian curve-fitting. The Ag 3d peaks (Figure 2a) for all thin films are located at 368.0 eV (3d5/2) and 374.0 eV (3d3/2), with a spin-orbit splitting of 6.0 eV. This is attributed to metallic Ag , consistent with the XRD result reported previously . By increasing the amount of Ag in the composite thin films, the Ag 3d peak shifts slightly to a lower binding energy position by only 0.1 eV (within experimental uncertainty).
The Ti 2p3/2 and 2p1/2 peaks (Figure 2b) are found at 458.1 and 463.5 eV, respectively, attributed to Ti4+ for pure crystalline TiO2 [34,35]. The peak position shows no critical change compared to that of pure TiO2. This indicates that there is no significant interfacial interaction between Ag and TiO2. The O 1s peaks (Figure 2c) found at 531.0 eV is due to O2− of TiO2 [34,36]. The Ti 2p and O 1s peaks are reduced in intensity. The O:Ti ratio obtained from XPS for TiO2, COMP-Agn (n =40, 50 and 70) are 2.003, 1.997, 2.007 and 2.130, respectively. Further, any peak around 457.4 eV attributable to the Ti3+ ion could not be observed .
2.2. The Distribution of Ag NP in the Ag-NP/TiO2 Composite Thin Films
The TEM images of all the composite thin films and Ag NP film are shown in Figure 3. As presented in Figure 3a, the presence and distribution of the Ag NP can be observed clearly as dark spots. Hence, the dark spots within the composite films micrographs (Figure 3b–j) represent the Ag NP. The high-resolution TEM image (Figure 3b) confirmed that the composite samples was comprised of crystalline titania and silver nanoparticles with the lattice spacing of a-axis agreeing well with the anatase phase (0.352 nm) and metallic silver (0.240 nm), respectively.
All the TEM micrographs (Figure 3a–j) exhibited small Ag-nanoparticles: 5 ± 2 nm. Three other populations of Ag NP are obtained; small spherical nanoparticles: 11 ± 7 nm, larger spherical: 29 ± 8 nm, and rod-like: 45 ± 25 nm, or agglomerated ones depending on the amount of silver in a given thin film. Therefore, COMP-Agn can be categorized into three types, as categorized by their UV/vis absorption spectra we indicated in recent work; low-Ag-level (10 ≤ n ≤ 40), middle-Ag-level (40 < n < 70), and high-Ag-level (70 ≤ n) composite thin films. The low-Ag-level thin films show spherical Ag NP homogeneously distributed in the titania with diameter 11 ± 7 nm. Most of Ag NP by the high-Ag-level thin films are more agglomerated, which is in contrast to the behaviors of the low- and middle-Ag-level thin films.
2.3. Particle Morphology and the Dispersion of Silver Nanoparticles
The surface morphology observed by FE-SEM of Ag-NP/TiO2 composite thin films is illustrated in Figure 4. The amounts of Ag grains (white dots) on the surface of low-Ag-level thin films (Figure 4a–d) were fewer and scattered compared to middle- and high-Ag-level thin films (Figure 4e–h), respectively. Figure 4e–f images for middle-Ag-level composite thin films illustrated that the surface morphology of three composite thin films, COMP-Ag50 and 60 respectively, are quite identical and Ag particles are homogeneously distributed with some spherical/rod-like and partially agglomerated Ag NP on the surface of the composite thin films. Figure 4g–h image shows high-Ag-level thin film, COMP-Ag 70 and 80, having a rough surface structure, with some spherical, rod-like and highly agglomerated Ag particles on the surface.
2.4. Optical Properties of TiO2 Thin Film, Ag-NPs and Ag-NP/TiO2 Composite Thin Films
Figure 5 represents the UV-vis absorption spectra for TiO2 and Ag NP. The TiO2 thin film showed a low-intensity absorption band in the vis-region; however, its absorption intensity increased steeply at shorter wavelengths with the band edge at around 355. In contrast, the Ag NP film showed a weak and broad absorption band at around 410 nm. The absorption band in this region corresponds to the characteristic SPR of Ag NPs . This absorption band was also observed for the COMP-Agn thin films, though the peak position in this region gradually increased in intensity upon increasing the Ag content .
The DRS of the composite thin films are presented in Figure 5(a−g). The DRS measured in the range of 200–800 nm were converted to the absorbance spectra using Kubelka-Munk equation (Equations 1 and 2) [37,38].
Where R is the reflectance recorded and RTiO2 is the reference recorded for a reference (titania in this case). The Origin9 software (OriginLaB Co., Northampton, MA, USA) was used to obtained individual Gaussian peaks, which are theoretically fitted peaks by assuming Gaussian distribution.
The peak positions and peak areas obtained by analysis with curve-fitting procedure are listed in Table 1. All the composites show two main peaks, labeled peak 2 and 3. Peak 2, which is at 365 nm on average, may represent a typical semiconductor optical absorption since the lambda maximum of pure TiO2 is at around 365 nm, corresponding to a band gap of around 3.4 eV. As shown in Figure 5, the band edge of TiO2 is around 365 nm and according to our recent paper , there was no band gap shift observed for TiO2 in all the composite thin films; therefore, we assign peak 2 in all the composites to be related to the TiO2 absorption spectrum. Peak 3, which is located at around 390 nm, can be regarded as the main Gaussian peak since it has the largest peak area ratio per volume compared to the other peaks.
|Table 1. The DRS peak positions and peak area ratios of Ag-NP/TiO2 composite thin films. These data were obtained by Gaussian curve-fitting using ORIGIN9 software (OriginLaB Co., Northampton, USA).|
|Notation||Peak position (λ nm)||Peak area ratio (%)|
Although the average lambda maximum peak position for peak 3 is at 390 nm, as shown in Figure 6a–h, more than one-third of its area cover, the visible region ≥400 nm. In addition, peak 1 is also exhibited in COMP-Ag10 as well as in the middle- and high-Ag-level composite thin films. Moreover, with exception to COMPAg60, overlapped Gaussians peaks with smaller peak areas than those of peak 2 and 3 are appearing in the visible light regions. These peaks 4, 5 and 6 have lambda maximum at around 500 nm, 600 nm and 550 nm, respectively.
2.5. Photo-Responsive Activity of Ag-NP/TiO2 Composite Thin Films
The photocatalytic activity of MB decoloration was investigated quantitatively by monitoring the changes between the initial MB absorption spectra and the final MB absorption spectra intensity positions, as well as qualitatively by determining the decoloration rate of MB (nM min−1). The absorption spectra of decoloration of 1 × 10−2 mM of MB aqueous solution tested under dark, UV light and vis-light irradiation for 18 h are shown in Figure 7a–c, respectively, by employing the pure TiO2 thin film, pure Ag NP, COMP-Agn thin films, where 10 ≤ n ≤ 80 and the blank.
Under dark (Figure 7a), the MB absorption spectra change for pure TiO2, pure Ag (Ag100) and COMP-Ag10 are at the identical intensity position to that of the blank. This illustrated that there was no catalytic activity taking place in these two samples under dark condition. The absorption spectra for COMP-Ag20, 30 and 40 show small changes compared to those of COMP-Ag50, 60 and 70. COMP-Ag80’s absorption spectral change is smaller than those of COMP-Ag 50, 60 and 70 composite thin films but larger than for low-Ag-level composite thin films. The influence of the amount of the Ag in titatia on self-decoloration of MB could be thus evaluated.
In Figure 7b, the absorption spectral changes is getting smaller with the increase in the Ag amount in COMP-Agn; whereby COMP-Ag80 and pure Ag NP (high-Ag-level) show the smallest changes and TiO2 shows the biggest change under UV-light irradiation. The pure Ag NP exhibited a very poor photocatalytic activity under UV and dark almost equal to that of the blank, which reflected that Ag did not act as catalytic on itself. Almost 100% decoloration of MB solution has been attained when UV-light was irradiated for 18 hours on pure TiO2 and on low-Ag-level composite thin films. Middle-Ag-level shows the moderated change between the initial MB absorption spectra and the final MB absorption spectra intensity positions. In Figure 7c, the absorption spectral change was larger with an increase in the amount of Ag in COMP-Agn thin film under visible-light irradiation. Pure TiO2 shows the smallest change, while COMP-Ag70 shows the largest change. Kőrösi et al. showed that the rate of photooxidation of organic compounds was significantly enhanced by silver-modification of titania .
In order to obtain qualitative data, an index of photocatalytic activity (IPCA, nM min−1) of decoloration rate of 1 × 10−2 mM MB solution permitted us to directly compare the performance of pure TiO2 and composite thin films under light irradiation to the dark condition. Each experimental set was repeated three times. The results were reproduced within narrow limits and the mean value was selected. The IPCA values extracted from a decoloration rate of 1 × 10−2 mM MB solution by photoreaction with each thin film and a blank are shown in Table 2.
Under UV-light irradiation, none of the composite samples exhibit more photoactivity than pure TiO2, while all of the composite samples are more photoactive than pure TiO2 under both dark and visible-light irradiation. The different results reveal that the photoactive enhancement mechanisms under UV and visible-light irradiation are different.
|Table 2. The index of photocatalytic activity (IPCA) of decoloration rate of 1.0 × 10−2 mM MB solution by photoreaction with each thin film and a blank.|
|Pure Ag NP||4.6(5)||3.3(3)||4.2(1)|
a The standard deviations are presented in parentheses.
2.6. Influence of Electrical Resistivity on Photocatalytic Decoloration Rate of the Composite Thin Films
In Figure 8, electrical resistivity and dependency of net photocatalytic decoloration rate (ΔIPCA) of each thin film as a function of Ag mol% in the Ag-NP/TiO2 composite thin films are presented. The electrical resistivity values are extracted from the paper we reported recently . The ΔIPCA value of each thin film is calculated as the difference between the IPCA under UV- or vis-light irradiation and the corresponding value measured for each thin film under dark conditions.
The low-Ag-level thin films show electrical resistivity higher than 106 Ω cm, the ΔIPCA values show a decrease trend under UV-light irradiation, and very lower ΔIPCA values slightly increasing under vis-light irradiation with the increase of Ag mol % in the composites. Middle-Ag-level composite thin films show low electrical resistivity in the range 10−1–10−4 Ω cm and their ΔIPCA values increases again toward the two-third level of the original TiO2 ΔIPCA value under UV-light irradiation. In contrary, the middle-Ag-level composite under vis-light irradiation shows the vis-response, whose level is slightly lower than the decreased UV-sensitivity of the identical thin film samples. A net photocatalytic activity local maximum appears between 60 and 70 mol% for vis-sensitivity. The electrical resistivity of high-Ag-level thin films is increasing from 10−5 Ω cm for COMP-Ag70 to higher than 106 Ω cm for COMP-Ag80, hence the acute decrease of the ΔIPCA value under both UV- and vis-light irradiation can be observed between 70 and 80 mol% of the Ag amount.
The photocatalytic activity of the Ag-NP/TiO2 composite thin films including those of unprecedentedly high Ag amounts was quantitatively examined by the decoloration reaction of MB in an aqueous solution. In Figure 8, the dependency of net photoreactivity (∆IPCA) of each thin film as a function of Ag mol% in the Ag NP/TiO2 composite thin films are presented, along with that of electrical resistivity. Each ΔIPCA value was calculated as the difference between the IPCA under UV- and vis-light irradiations and the corresponding value measured for each thin film under dark conditions (Table 1) [40,41]. The IPCA under dark condition can be representing both adsorption and self-decoloration of MB [42,43], and they are dependent on the Ag amount in the thin films. The IPCA of pure Ag NP is slightly high under visible light compare to those under UV-light and dark; this could be due to the plasmonic photocatalyst associated with Ag nanoparticles .
3.1. Photocatalytic Activity under UV-Light Irradiation
As shown in Figure 8, the ΔIPCA of the composites under UV irradiation has two points of inflection depending on the Ag amount in the composites. One appears at 40 mol% as a local minimum and another at 60 mol% as a local maximum.
The high ∆IPCA values of the composites whose Ag amounts to up to 30 mol% indicates UV-sensitivity almost identical to anatase thin films . The decreasing tendency of the activity in this region is due to both the decreases of anatase in TiO2  and the TiO2 amount in the composites by increasing the Ag amount in the composites. The photocatalytic activity of TiO2 under UV-light irradiation should be due to the anatase form of TiO2 in the thin films and not to the rutile form , because it was indicated that the photocatalytic activity of these composite thin films is not owing to the oxygen deficiency by the present XPS analysis (Figure 1).
The acute decrease of the activity occurs between 30 and 40 mol% of the Ag amount which critically corresponds to the percolation threshold of electrical conductivity of the composites . The ΔIPCA decrease of the composite thin films due to TiO2 components under UV-light irradiation is thus inevitable by the decrease of anatase with the increase of Ag NP. This tendency should be accelerated by increasing the Ag amount in the composites, because the covering of the TiO2 surfaces by the deposited Ag particles occurs significantly even if the Ag NP distribute homogeneously (Figure 3, Figure 4).
It can be therefore accepted that the decrease of the photocatalytic activity by anatase under UV-irradiation should be consecutive with the increasing amount of Ag NP. However, the ΔIPCA value increases again toward the local maximum whose position deviates slightly from that of the lowest electrically resistivity of the composite thin films, at 60 mol% of Ag amount in the composite. Consequently, the activity recovery to a two-third level of the original TiO2 may be assisted by the enhanced electrical conductivity of the composite. The slight difference between the local-minimum position of the photocatalytic activity and that of the electrical resistivity suggests that the anatase amount in the composites is more effective than the electrical resistivity.
3.2. Photocatalytic Activity under Vis-Light Irradiation
We have shown in Figure 7c that the increase in the amount of Ag in the composite consistently increased the vis-sensitivity of the composite thin films. This increase in vis-sensitivity of the composite was not only significant, but relatively large in magnitude (Figure 8). The synergistic effect can be interpreted as the result of the excellent adsorption capabilities of the Ag NP combined with the advantageous effect of silver nanoparticles on light absorption in the visible range [28,29]. While there were general positive effects on photocatalytic activity with the increase in the amount of Ag in the composite of up to 70 mol% of Ag amount in the composite, an acute decrease of the ΔIPCA value can be observed between 70 and 80 mol% of the Ag amount. Collectively, these results suggest that the ultimate impact of Ag NP on composite thin films’ photocatalytic activity may be quite predictable. However, the mechanistic basis for vis-sensitivity could be difficult to understand and predict without a good deal of optical absorption spectra [26,27]. Therefore, the optical absorption of AgNP/TiO2 composite thin films were characterized by UV/vis DRS (Figure 4) in order to study the apparition of different resonant absorption peaks caused by the difference in amounts of Ag in the composite.
3.2.1. Contribution of SPR and LSPR in Photocatalytic Activity under Vis-Light Irradiation
In Figure 6, when the composite has less than or equal to 70 Ag mol% it is possible to appreciate only a DRS peak 3 (black dotted line). This first well-defined DRS peak was found centered at around ca. 390 nm (peak 3), and it is attributed to the natural optical resonance of spherical Ag NP [12,14]. Although this peak is centered around 390 nm, about one-third of its area in all the composite thin films belongs to visible light region (≥400 nm). The lamp used to study the decoloration of MB aqueous solution employed in this study doe emit 0.8 mWcm−2 at a wide range of 400 nm–800 nm, which is sufficient to stimulate visible light photocatalytic activity even for the area that cover by the SPR peak 3. All the composites exhibit this SPR peak 3, and are therefore reflecting their capability to respond to visible light. Whereby, peak 3 takes the potential advantage of being present in the same visible spectra widow of the natural optical SPR of spherical Ag NP.
In addition, all the composite thin films showed a typical semiconductor optical absorption band with a lambda maximum peak at around ca. 365 nm (peak 2), which corresponded to the band gap of pure TiO2, and that is only responsible for UV-sensitivity  and hence not important for vis-sensitivity. Titanium dioxide displays photocatalytic behavior under UV illumination. However, other DRS peaks (peak 1, 4, 5 and 6) are assignable to localized surface plasmon resonance (LSPR). Size-shape-dependent LSPR occur when metallic Ag NP with a different size, shape and separation distance are irradiated by light, whereby large oscillating electric fields are produced between the metal nanoparticles . Therefore, these plasmonic properties of the Ag NP/TiO2 composite thin films can help us in elucidating the mechanism behind photocurrent generation by Ag NP/TiO2 composite thin films. (1) Due to LSPR, electrons from Ag NPs are promoted to higher states in the band. (2) These electrons are then injected into the conduction band of TiO2 and defuse to catalytically active sites at the semiconductor/liguid interface where they drive chemical transformations [9,41]. The proposed mechanism is already confirmed by the experiments of transient photocurrent response [12,33].
TEM and SEM micrographs (Figure 3, Figure 4) corroborate that the composites have Ag NPs with different size and shapes. XPS results show that Ag NPs are metallic. The metallic property of the Ag NP in our composite thin film is consistent with the XRD we reported recently . Usually, Ag/TiO2 thin films are short-lived because Ag NPs on TiO2 are easily oxidized under vis-light irradiation; therefore, no plasmonic photocatalyst was observed unless the Ag core is covered with a silica (SiO2) shell  or masked with an Al2O3 nanomask  to prevent oxidation of Ag by direct contact with TiO2. Molecular precursor method enables plasmonic photocatalysis without covering the metallic Ag core in the composite.
3.2.2. Contribution of Electrical Conductivity on the Photocatalytic Activity
Something to be noted is that the dependency of net photocatalytic decoloration rate ∆IPCA of middle-Ag-level composite thin films was significantly higher than that for low- and high-Ag-level composite thin films (Figure 8). It is interesting that the net photocatalytic decoloration rates of the composite thin films are strongly correlated to their electrical resistivity rather than to the number of LSPR peaks that appeared in the visible region. The low-Ag-level thin films show resistivity higher than 106 Ω cm and exhibit the poorest photocatalytic activity under visible light irradiation. These films could still easily absorb photons to produce photoexcited electrons under vis light due to SPR and LSPR DRS peaks in visible light region. However, the movement of these photoexcited electrons is difficult because of very high electrical resistivity associated with low-Ag-level composite thin films . Hence, this is leading to an increase in extinction probability, which is unfavorable to the photoresponsive activity of the thin film.
On the other hand, the middle-Ag-level thin films show low electrical resistivity in the range 10−1–10−5 Ω cm  and high photocatalytic activity, which gradually increases with an increase in the amount of Ag NP on the surface of titania. The increase of Ag NP on the surface of titania may result in a lower electron density of the Ti atoms in the Ag/TiO2 samples. However, it is widely accepted that the Ag NPs in TiO2 will benefit the separation of photogenerated electron-hole pairs due to electrical conductivity, thus enhancing the photocatalytic activity .
The electrical resistivity of the high-Ag-level thin films increases again from 10−5 Ω cm–10−2 Ω cm  with an increase in the amount of Ag in titania from 70 mol%–80 mol%, respectively. At the same time, the photocatalytic activity of the high-Ag-level thin films has acute decreases with an increase in the amount of Ag from 70 mol%–80 mol%, respectively. This reveals that the electrical conductivity of Ag-NP/TiO2 composite thin film is important for the higher photocatalytic decoloration rate observed under both UV and vis-light irradiation. Thus, the electrical conductivity property of the thin film facilitates the transportation of extra electrons to the conduction band, which in turn are able to produce more reactive species at the titania surface , blocking electron–hole recombination which stops the production of radicals at the surface .
4. Experimental Section
Ethylenediamine-N,N,N′,N′-tetraacetic acid (EDTA) and titanium tetraisopropoxide (Ti(OiPr)4) were purchase from Kanto Chemical Co., Inc. Tokyo, Japan. 30% H2O2 were purchased from Santoku Chemical Industries Co., Ltd. Tokyo, Japan, respectively. Silver acetate, methylene blue (MB) and dibutylamine were purchased from Wako Pure Chemical industries, Ltd. Methanol and 2-propanol were purchased from Taisei Chemical Co., Ltd., Tokyo, Japan while ethanol was purchased from Ueno Chemical Industries, Ltd., Tokyo, Japan and dried on 4A molecular sieves prior to use. Other materials were used without further purification. Polished quartz glass was purchased from Akishima Glass Co., Ltd. (Tokyo, Japan). The quartz glass substrates of 20 × 20 × 1.1 mm3 were prepared and cleaned in 2-propanol with an ultrasonic bath to remove physisorbed organic molecules from the surfaces, followed by rinsing several times with de-ionized water. Then the substrates were dried in a drying oven at 70 °C. NaCl single crystals were purchased from MANAC Incorporated (Tokyo, Japan). Cu grid plates were purchased from NISSHIN EM Co. (Tokyo, Japan).
4.2. Preparation of Coating Precursor Solutions, STi, SAg and Scomposite
As shown in Scheme 1(a), the precursor solution STi contains a Ti4+ complex of EDTA was prepared in accordance with the molecular precursor method (MPM) reported in our previous studies [30,31,32,33]. The ethanol solution of Ag-nanoparticle, SAg for fabrication of Ag-nanoparticles titania thin film was also prepared separately based on the method that we reported recently  and Scheme 1b shows how the silver precursor solution SAg was synthesized. For Ag nanoparticle suspensions, a common method is the Lee-Meisel method, which is a variation of the Turkevich method in that Ag nitrate is used as the metal source [22,46]. The application of acetate in the reaction allowed synthesizing metallic nanoparticles without any additional reducer. It makes that kind of synthesis simple, fast, and relatively cheap, and makes it possible to obtain pure composites without any impurities, which is a big advantage when compared to the reduction of silver nitrate [23,34]. The Scomposite, with different compositions, was achieved by mixing a certain amount of SAg with STi. Then, the Scomposite was sonicated with stirring for 5 min to increase the homogeneity.
4.3. Fabrication of Ag-Nano Particle-Titania Thin Films on Quartz Glass
Before the deposition of Scomposite, quartz glass substrates (volume: 20 × 20 × 1.1 mm3) was cleaned using the procedure reported in our recent paper . Then, the wafers were dried in a drying oven at 70 °C. The Ag-nanoparticle/titania composite (COMP-Agn) films were fabricated by heat treating the spin-coated precursor films, while applying the solution Scomposite. The number n in the notation of the composite films indicates the silver molar percentage (Ag mol%) to TiO2; for example, the name COMP-Ag50 indicates that the silver molar percentage in the Scomposite solution was 50 mol%. The Ag-NP/TiO2 composite thin films were deposited by spin coating of the Scomposite onto the substrates with a double step mode: first at 500 rpm for 5 s and then at 2000 rpm for 30 s in all the cases. Thin films were fabricated by heat-treatment at 600 °C for 0.5 h to remove residual organic compounds. Ag-NP/TiO2 composite ultra-thin films used to measure the TEM images of the composite was also prepared using the same procedure, except that the thin film was fabricated on NaCl single crystals as a supportive substrate and the ultra-thin films were transfer on Cu grid upon.
4.4. Characterization of Ag-NP/TiO2 Composite Thin Films
A Phi Quantum 2000 Scanning ESCA Microprobe (Shimadzu, Tokyo, Japan) with a focused monochromatic Al-Kα X-ray (1486.6 eV) source was employed in order to evaluate the elemental states and quantities―Ti, O, C and Ag―in the thin films. No critical surface charging during the XPS measurements was observed; thereby, no correction of binding energy was performed. The depth profiles were obtained with the identical instrument. The stepwise etching was performed by bombarding the Ar+ ions with 2 kV for 3 min before measuring each layer.
4.5. Surface morphology and Measurement of Optical Properties of Ag-NP/TiO2 Composite Thin Films
The surface morphology of the all resulting composite thin films was observed with a field-emission scanning electron microscope (FE-SEM S-4200, Hitachi, Tokyo, Japan) at an accelerating voltage of 0.5 kV. The nanostructure images for Ag-NP/TiO2 composite thin films were observed with a transmission electron microscope (TEM H8100, Hitachi, Tokyo, Japan) at an accelerating voltage of 120 kV using the ultra-thin films applied on Cu grid. The reflectance spectra of pure TiO2 as well as for those of the Ag-NP/TiO2 composite thin film samples were performed with a Perkin-Elmer Lambda 35 spectrometer provided with a diffuse reflectance accessory
4.6. Photocatalytic Measurement of TiO2 Thin Film and Various Ag-NP/TiO2 Composite Thin Films
The study of the decoration of methylene blue aqueous solution was done using the method adapted in our laboratory [40,47]. Here, the photocatalytic activity of pure TiO2 and composite thin films was estimated by measuring the decoloration rate of methylene blue (0.01 mM) in an aqueous solution (10 mL) containing 20 × 20 mm2 thin film photocatalyst. Various Ag-NP/TiO2 composite thin films with different Ag molar concentration or pure TiO2 thin film was used as the photocatalyst. The photocatalysts were immersed in the 0.02 mM MB aqueous solutions overnight in the dark to allow equilibrate adsorption on the film surfaces.
For UV measurements, the suspension was irradiated using a black light, National FL10BL-B, which emits UV light. The distances of the black light sources from sample surfaces were adjusted to maintain UV intensities at 365 nm of 1.2 mW cm−2 which was measured by an UV meter, UVR-400, Iuchi Co., Ltd. (Tokyo, Japan). Vis-light was obtained from a fluorescent light, Duro-Test Vita-Lite, by removing light of wavelengths shorter than 400 nm using a cut-off filter, Ishihara Window Paint. The vis-light intensity after removing UV components from the fluorescent light, which was estimated by an illuminometer, LX-105, CUSTOM Co., Ltd. (Tokyo, Japan) was 0.8 m W cm−2. In order to examine the degree of adsorption on the glass substrate and self-decomposition of MB, same measurement was performed on the same samples without irradiation (dark) as a reference.
The MB concentration was determined by measuring the absorption spectra of the aqueous solution with the U-2800 spectrophotometer. For the decoloration test, ca. 3 mL of the 0.01 mM MB aqueous solution was transferred into a quartz cell of dimensions 1 W × 1 L × 4.5 H cm3 at 20-min intervals. After spectral measurement in the range of 600–700 nm, the solution was immediately returned to the vessel and mixed with the aliquot. The mixed solution continued to be used until the test for each film was completed. The mixed solution was further used until the test for each film was done again after 18 h. The absorption peak value at 664 nm were used in order to determine the concentration of MB after t minutes, C(t), using Equation 3:
The decoloration rate of MB was examined three times for each film, and the initial decoloration rate (k) values of concentration after t minutes of 0.01 µM MB aqueous solution by photoreaction with each potential photocatalytic thin film and a blank were measured by an approximate line for the function of C(t) versus t obtained in the range from 0 ≤ t ≤ 180 min by a least-square method. The index of photocatalytic activity (IPCA) of the film was estimated from the averaged value of k, using equation 4 adapted from [40,48].
In this work, the photocatalytic activity of the Ag-NP/TiO2 composite thin films including those of unprecedentedly high Ag amounts (10–80 molar%) was quantitatively examined by the decoloration reaction of methylene blue (MB) in an aqueous solution. Different attenuation DRS absorption sharp peaks have been obtained in the 310 nm−710 nm spectra range. Two of these peaks is inherent to the natural optical SPR of spherical Ag NP (the peak around 390 nm) and to the typical pure TiO2 optical absorption (the peak around 365 nm), respectively. All the composites exhibit these two peaks, reflecting the capability to respond to both UV and visible light. On the other hand the size- and shape-dependent LSPR peaks appear at different lambda maximum. An analysis of DRS spectra of the obtained composites proved that Ag NP absorption visible light, facilitated by surface plasmon absorption of the composite thin films. Hence, the findings demonstrated that a positive relationship exists between Ag NP surface plasmon absorption and the rate enhancements, and proves the hypothesis that the metallic plasmon enhances rates of photocatalytic reaction, as enhanced by the electrical conductivity of the thin film.
This work was supported by the “Energy Conversion Ecomaterials Center” project: Matching fund subsidy from MEXT (Ministry of Education, Culture, Sports, Science and Technology), Japan.
Conflict of Interest
The authors declare no conflict of interest.
- Fujishima, A.; Rao, T.N.; Truk, D.A. Titanium dioxide photocatalysis. J. Photochem. Photobiol. C 2000, 1, 1–21, doi:10.1016/S1389-5567(00)00002-2.
- Fujishima, A.; Honda, K. Electrochemical photolysis of water at a semiconductor electrode. Nature 1972, 238, 37–38, doi:10.1038/238037a0.
- Rehman, S.; Ullah, R.; Butt, A.M.; Gohar, N.D. Strategies of making TiO2 and ZnO visible light active. J. Hazard. Mater. 2009, 170, 560–569, doi:10.1016/j.jhazmat.2009.05.064.
- Hamal, D.B.; Klabunde, K.J. Synthesis, characterization, and visible light activity of new nanoparticle photocatalysts based on silver, carbon, and sulfur-doped TiO2. J. Colloid Interface Sci. 2007, 311, 514–522, doi:10.1016/j.jcis.2007.03.001.
- Kőrösi, L.; Bertóti, S.P.I.; Dékány, I. Surface and bulk composition, structure and photocatalytic activity of phosphate modified TiO2. Chem. Mater. 2007, 19, 4811–4819, doi:10.1021/cm070692r.
- Körösi, L.; Oszkó, A.; Galbács, G.; Richardt, A.; Zöllmer, V.; Dékány, I. Structural properties and photocatalytic behaviour of phosphate-modified nanocrystalline titania films. J. Appl. Catal. B 2007, 77, 175–183, doi:10.1016/j.apcatb.2007.07.019.
- Janovák, L.; Veres, Á.; Bujdosó, T.; Rica, T.; Fodor, E.; Tallósy, S.; Buzás, N.; Nagy, E.; Dékány, I. Silver and phosphate functionalized reactive TiO2/polymer nanocomposite films for destructions resistant bacteria using visible light. J. Adv. Oxid. Technol. 2011, 15, 205–216.
- Loganathan, K.; Bommusamy, P.; Muthaiahpillai, P.; Velayutham, M. The syntheses, characterizations, and photocatalytic activities of silver, platinum, and gold doped TiO2 nanoparticles. Environ. Eng. Res. 2012, 16, 81–90.
- Liu, S.X.; Qu, Z.P.; Han, X.W.; Sun, C.L. A mechanism for enhanced photocatalytic activity of silver-loaded titanium dioxide. Catal. Today 2004, 93–95, 877–884.
- Jakob, M.; Levanon, H.; Dame, N. Charge distribution between UV-irradiated TiO2 and gold nanoparticles: Determination of shift in the fermi level. Nano Lett. 2003, 3, 353–358, doi:10.1021/nl0340071.
- Hirakawa, T.; Kamat, P.V. Charge Separation and Catalytic Activity of Ag@TiO2 Core-Shell Composite Clusters under UV-Irradiation. J. Am. Chem. Soc. 2005, 127, 3928–3934, doi:10.1021/ja042925a.
- Yu, J.; Dai, G.; Huang, B. Fabrication and characterization of visible-light-driven plasmonic photocatalyst Ag/AgCl/TiO2 nanotube arrays. J. Phys. Chem. C 2009, 113, 16394–16401, doi:10.1021/jp905247j.
- Dahmen, C.; Sprafke, A.N.; Dieker, H.; Wuttig, M.; von Plessen, G. Opticaland structural changes of silver nanoparticles during photochromic transformation. Appl. Phys. Lett. 2006, 88, 11923, doi:10.1063/1.2163268.
- Standridge, S.D.; Schatz, G.C.; Hupp, J.T. Toward Plasmonic Solar Cells: Protection of Silver Nanoparticles via Atomic Layer Deposition of TiO2. Langmuir 2009, 25, 2596–600, doi:10.1021/la900113e.
- Wodka, D.; Bielańska, E.; Socha, R.P.; Elzbieciak-Wodka, M.; Gurgul, J.; Nowak, P.; Warszyński, P. Photocatalytic activity of titanium dioxide modified by silver nanoparticles. ACS Appl. Mater. Interfaces 2010, 2, 1945–1953, doi:10.1021/am1002684.
- Rad, B. Enhancement of photocatalytic activity of TiO2 nanoparticles by silver doping: photodeposition versus liquid impregnation methods. Global NEST J. 2008, 10, 1–7.
- Turkevich, J.; Stevenson, P.C.; Hillier, J. A study of the nucleation and growth processes in the synthesis of colloidal gold. Discuss. Faraday Soc. 1951, 11, 55, doi:10.1039/df9511100055.
- Enustun, B.V.; Turkevich, J. Coagulation of colloidal gold. J. Am. Chem. Soc. 1963, 85, 3317, doi:10.1021/ja00904a001.
- Frens, G. Controlled nucleation for the regulation of the particle size in monodisperse gold suspensions. Nat. Phys. Sci. 1973, 20, 241.
- Kumar, K.P.; Paul, W.; Sharma, C.P. Green synthesis of silver nanoparticles with zingiber officinale extract and study of its blood compatibility. BioNanoScience 2012, 2, 144–152, doi:10.1007/s12668-012-0044-7.
- Kuntyi, O.; Okhremchuk, Y.; Bilan’, O.; Hapke, J.; Saldan, I. Silver particles growth by pulse electrolysis in acetonitrile solutions. Central Eur. J. Chem. 2013, 11, 514–518, doi:10.2478/s11532-012-0189-9.
- Patakfalvi, R.; Papp, S.; Dékány, I. The kinetics of homogeneous nucleation of silver nanoparticles stabilized by polymers. J. Nanopart. Res. 2007, 9, 353–364, doi:10.1007/s11051-006-9139-9.
- Seery, M.K.; George, R.; Floris, P.; Pillai, S.C. Silver doped titanium dioxide nanomaterials for enhanced visible light photocatalysis. J. Photochem. Photobiol. 2007, 189, 258–263, doi:10.1016/j.jphotochem.2007.02.010.
- Grabowska, E.; Zaleska, A.; Sorgues, S.; Kunst, M.; Etcheberry, A.; Colbeau-Justin, C.; Remita, H. Modification of titanium(IV) dioxide with small silver nanoparticles: application in photocatalysis. J. Phys. Chem. C 2013, 117, 2013.
- Li, H.; Zhao, G.; Song, B.; Han, G. Effect of incorporation of silver on the electrical properties of sol-gel-derived titania film. J. Cluster Sci. 2008, 19, 667–673, doi:10.1007/s10876-008-0207-4.
- Takahashi, Y.; Tatsuma, T. Electrodeposition of thermally stable gold and silver nanoparticle ensembles through a thin alumina nanomask. Nanoscale 2010, 2, 1494–1499, doi:10.1039/c0nr00230e.
- Awazu, K.; Fujimaki, M.; Rockstuhl, C.; Tominaga, J.; Murakami, H.; Ohki, Y.; Yoshida, N.; Watanabe, T. A plasmonic photocatalyst consisting of silver nanoparticles embedded in titanium dioxide. J. Am. Chem. Soc. 2008, 130, 1676–1680, doi:10.1021/ja076503n.
- Ménesi, J.; Kékesi, R.; Oszkó, A.; Zöllmer, V.; Seemann, T.; Richardt, A.; Dékány, I. Photocatalysis on silver-layer silicate/titanium dioxide composite thin films at solid/vapour interface. Catal. Today 2009, 144, 160–165, doi:10.1016/j.cattod.2009.02.030.
- Ménesi, J.; Kékesi, R.; Zöllmer, V.; Seemann, T.; Richardt, A.; Dékány, I. Photooxidation of ethanol on Cu-layer silicate/TiO2 composite thin films. React. Kinet. Calal. Lett. 2009, 96, 367–377, doi:10.1007/s11144-009-5532-6.
- Sato, M.; Hara, H.; Niside, T.; Sawada, Y. A Water-resistant precursor in a wet process for TiO2 thin film formation. J. Mater. Chem. 2006, 6, 1767–1770.
- Nagai, H.; Aoyama, S.; Hara, H.; Mochizuki, C.; Takano, I.; Honda, T.; Sato, M. Photoluminescence and photoreactivity affected by oxygen defects in crystal-oriented rutile thin film fabricated by molecular precursor method. J. Mater. Sci. 2010, 45, 5704–5710, doi:10.1007/s10853-010-4640-z.
- Likius, D.S.; Nagai, H.; Aoyama, S.; Mochizuki, C.; Hara, H.; Baba, N.; Sato, M. Percolation threshold for electrical resistivity of Ag-nanoparticle/titania composite thin films fabricated using molecular precursor method. J. Mater. Sci. 2012, 47, 3890–3899, doi:10.1007/s10853-011-6245-6.
- Daniel, L.S.; Nagai, H.; Sato, M. Photoelectrochemical property and the mechanism of plasmonic Ag-NP/TiO2 composite thin films with high silver content fabricated using molecular precursor method. J. Mater. Sci. 2013, doi:10.1007/s10853–013–7533–0.
- Kang, J.-G.; Sohn, Y. Interfacial nature of Ag nanoparticles supported on TiO2 photocatalysts. J. Mater. Sci. 2012, 47, 824–832, doi:10.1007/s10853-011-5860-6.
- Wan, L.; Li, J.F.; Feng, J.Y.; Sun, W.; Mao, Z.Q. Improved optical response and photocatalysis for N-doped titanium oxide (TiO2) films prepared by oxidation of TiN. Appl. Surface Sci. 2007, 253, 4764–4767, doi:10.1016/j.apsusc.2006.10.047.
- He, W.F.Z.Y.L.; Zhang, M.S.; Yin, Z.; Chen, Q. Raman scattering study on anatase TiO2 nanocrystals. J. Phys. D 2000, 33, 912, doi:10.1088/0022-3727/33/8/305.
- Li, J.; Xu, J.; Dai, W.; Fan, K. Dependence of Ag Deposition Methods on the Photocatalytic Activity and Surface State of TiO2 with Twistlike Helix Structure. J. Phys. Chem. C 2009, 113, 8343–8349.
- Kortum, G. Reflectance Spectroscopy; Springer-Verlag: Berlin, Germany, 1969; p. 180.
- Kőrösi, L.; Papp, S.; Ménesi, J.; Illés, E.; Zöllmer, V.; Richardt, A.; Dékány, I. Photocatalytic activity of silver-modified titanium dioxide at solid-liquid and solid-gas interfaces. Colloids Surfaces A 2008, 319, 136–142, doi:10.1016/j.colsurfa.2007.11.030.
- Nagai, H.; Mochizuki, C.; Hara, H.; Takano, I.; Sato, M. Enhanced UV-sensitivity of Vis-responsive Anatase Thin Films Fabricated by Using Precursor Solutions Involving Ti Complexes. Solar Energy Mater. Solar Cell. 2008, 92, 1136–1144, doi:10.1016/j.solmat.2008.04.005.
- Christopher, P.; Xin, H.; Linic, S. Visible-light-enhanced catalytic oxidation reactions on plasmonic silver nanostructures. Nat. Chem. 2011, 3, 467–472.
- Li, H.; Bian, Z.; Zhu, J.; Huo, Y.; Li, H.; Lu, Y. Mesoporous Au/TiO2 nano-composites with enhanced photocatalytic activity. J. Am. Chem. Soc. 2007, 129, 4538, doi:10.1021/ja069113u.
- Kosanic, M.M. Photocatalytic degradation of oxalic acid over TiO2 power. J. Photochem. Photobiol. A 1998, 119, 119–122, doi:10.1016/S1010-6030(98)00407-9.
- Kiyonaga, T.; Mitsui, T.; Torikoshi, T.M.; Takekawa, M.; Soejima, T.; Tada, H. Ultrafast photosynthetic reduction of elemental sulfur by Au nanoparticle-loaded TiO2. J. Phys. Chem. B 2006, 110, 10771, doi:10.1021/jp061528e.
- Yang, X.; Wang, Y.; Xu, L.; Yu, X.; Guo, Y. Silver and indium oxide codoped TiO2 nanocomposites with enhanced photocatalytic activity. J. Phys. Chem. C 2008, 112, 11481–11489, doi:10.1021/jp803559g.
- Lee, P.C.; Meisel, D.J. Adsorption and surface-enhanced Raman of dyes on silver and gold sols. Phys. Chem. 1982, 86, 3391–3395, doi:10.1021/j100214a025.
- Nagai, H.; Hasegawa, M.; Hara, H.; Mochizuki, C.; Takano, I.; Sato, M. An important factor controlling the photoreactivity of titania: O-deficiency of anatase thin film. J. Mater. Sci. 2008, 43, 6902–6911, doi:10.1007/s10853-008-2993-3.
- Nagai, H.; Aoyama, S.; Hara, H.; Mochizuki, C.; Takano, I.; Baba, N.; Sato, M. Rutile thin film responsive to visible light and with high UV light sensitivity. J. Mater. Sci. 2009, 44, 861–868, doi:10.1007/s10853-008-3185-x.
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