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International Journal of Photoenergy
Volume 2012 (2012), Article ID 913630, 7 pages
Research Article

Enhancing Photocatalytic Performance through Tuning the Interfacial Process between -Assembled and Pt-Loaded Microspheres

1School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China
2State Key Lab of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China
3Key Lab of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China

Received 10 November 2011; Accepted 2 December 2011

Academic Editor: Jiaguo Yu

Copyright © 2012 Jun Zhang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


This work reports on a simple two-step approach to rutile TiO2-assembled microspheres loaded by Pt with an aim to tune semiconductor-metal interfacial processes for enhancing the photocatalytic performance. Systematic sample characterizations and structural analysis indicate that Pt loading did not produce any significant influences on the lattice structure of TiO2-assembled microspheres. Instead, upon Pt loading, Schottky barrier was formed in the interfaces between microspheres and Pt nanoparticles, which inhabited efficiently the recombination of photo-generated electron-hole pairs essential for the photocatalytic activities. In addition, TiO2 microspheres also showed a capacity of electrons storage and releasing as represented by a high dielectric constant, which increased the utility rate of photogenerated electrons. All these structural advantages contribute to the excellent photocatalytic activity under ultraviolet light irradiation. The interfacial process between microspheres and Pt nanoparticles was further tuned through adjusting the loading Pt content of metal Pt. As a consequence, the best photocatalytic activity on TiO2 was obtained at 0.85 wt% Pt loading, above or below which photocatalytic activity was apparently decreased.

1. Introduction

Degradation of organic pollutants by photocatalytic technology has attracted increasing attention [1, 2]. In all kinds of photocatalysts, simple oxide semiconductors (e.g., TiO2, ZnO, and SnO2) have been extensively studied [36], among which TiO2 nanomaterials characterized by the advantages of nontoxicity, stability, cheapness, and high activity have become the basis of promising photocatalysts [7, 8]. However, due to the wide bandgap and low quantum efficiency, the practical applications are always restricted [911]. Therefore, some endeavors (like doping foreign elements [12, 13] and coupled semiconductors or composites [5]) have been implemented, and some gains are obtained. Even so, efficient methods in enhancing photocatalytic activity are still challenging, since the elements introduced into the semiconductors often act as the recombination of photogenerated electrons and holes that would decrease the quantum efficiency.

One has to execute some other routes such as imputing external fields or depositing some noble metals. For example, when H2 [14] and magnetic field [15] are involved into the systems, the photocatalytic activities can be significantly improved, while the reaction systems became complicated, seemly not favorable for comprehension of photocatalytic process. In addition, loading noble metal (e.g., Au, Ag, Pt, Pd) onto semiconductors has been observed to greatly improve the photocatalytic activity [9, 1618], in which the efficient utility of photogenerated electrons in the photo-degradation process is critical but often ignored.

In this work, we synthesized TiO2-assembled microspheres with different Pt loading content through microsphere formation with a subsequent photoreduction deposition of Pt nanoparticles. With tuning the loading quantity of metal Pt, an optimum photocatalytic activity was achieved at a loading of 0.85 wt% Pt. Further, the impacts of Pt loading content were investigated as a measure for the interfacial process between microspheres and Pt nanoparticles responsible for the enhanced photocatalytic activities.

2. Experimental Section

2.1. Sample Preparation

All reagents employed in the experiments were analytical grade and used without further purification. TiO2 microspheres were of fabricated according to the solution chemistry described in our previous work [19]. Briefly, 20.5 mL TiCl4 (Alpha, 99%) was added dropwise into 60 mL distilled water at 0°C in an ice-water bath under vigorously magnetic stirring to form a given concentration aqueous solution. After stirring for about 1 h, the solution was transferred to a Teflon-lined stainless steel autoclave (100 mL). After reaction at 160°C for 2 h, the autoclave was allowed to cool to room temperature naturally, and the final product was washed carefully with distilled water to remove Cl in the residue solution. The resulting product was dried at 80°C for 4 h in air.

Pt-deposited TiO2 microspheres were prepared via a photoreduction process. Generally, 0.5 g of the as-prepared TiO2 microspheres was immersed into 100 mL solution of H2PtCl4 (Sino-Platinum Co., Ltd.) in distilled water. 0.1 M acetic acid (Sinopharm Chemical Reagent Co., Ltd.) was used to adjust the pH of suspension to about 3. Then, high-purity nitrogen passes through the suspension for 15 min to remove the oxygen in suspension. After stirring for 3 h, the mixture solution was irradiated for 3.5 h by a 300 W high-pressure xenon lamp while stirring. Finally, the specimen was centrifuged and washed with distilled water until no Cl was detected in the rinsing water. The quantity of H2PtCl4 needed was set according to the mass ratio of metal Pt to TiO2 as 0.1 wt%, 0.5 wt%, 1.0 wt%, and 3 wt%, and the corresponding samples were named as 0.1-Pt-TiO2, 0.5-Pt-TiO2, 1.0-Pt-TiO2, and 3.0-Pt-TiO2. After being dried in vacuum at 80°C, the resulting products were obtained.

2.2. Sample Characterization

Powder X-ray diffraction (XRD) patterns of the samples were collected on Rigaku MinFlex benchtop X-ray diffractometer with Cu Kα irradiation. The crystallite sizes for the samples were calculated according to Scherrer formula, , where is the X-ray wavelength employed, is the diffraction angle matches along with diffraction peak (110), and is defined as the peak width at half height after the instrumental broadening is subtracted. The lattice parameters of the samples were calculated by a least-squares method using Rietica Rietveld software. Ni powder serves as an internal standard for peak position determination. Morphologies of the samples were observed by field emission scanning electron microscopy (FE-SEM) (JEOL JSM-6700). The specific loading contents of Pt for all samples were measured by Inductively Coupled Plasma OES spectrometer (ICP) (Ultima2). UV-vis diffuse reflectance spectra of the samples were obtained using a Varian Cary 500 UV-vis-NIR spectrometer. Infrared spectra of the samples were measured on a Perkin-Elmer IR spectrophotometer at a resolution of 4 cm−1 using the KBr pellet technique.

2.3. Photocatalytic Activity Evaluation

Photocatalytic activities test of samples was implemented on a UV light photoreactor, which was constructed by a quartz tube (4.6 cm in inner diameter and 17 cm in length) surrounded by four UV lamps ( , 4 W). Methyl orange (MO) was taken as a probe molecule for evaluating the photocatalytic activity. All experiments were performed at room temperature. Namely, 100 mg of the sample was dispersed in 100 mL MO (10 mg/L) solution and magnetically stirred for 5 h to establish adsorption/desorption equilibrium of MO solution on the sample surfaces before illumination. Then, the suspension solution was irradiated by light and collected at a regular time interval. Finally, the collected solution was centrifuged at a rate of 8500 rpm to remove the solid power and UV-vis absorption spectra of the supernatant were measured with a Perkin-Elmer UV lambda 35 spectrophotometer.

3. Results and Discussion

Figure 1 shows the SEM images of pure TiO2 and 1.0-Pt-TiO2 samples. It is explicit to found that pure TiO2 sample exhibits a microsize spherical morphology as constructed by bundles of nanowires, in which nanowires grew from the center of microsphere to the outward surface along with the direction , exposing the outer surface (110) of nanowire and tip (001) of nanowire while keeping a roughly parallel configuration [19]. Upon photoreduction deposition, very small Pt particles are dispersed uniformly onto the microspheres, since there are no obvious changes in the microsphere morphology. Further, Pt deposited onto the microspheres is in metallic state as indicated by XPS and TEM [20].

Figure 1: SEM images of the samples: (a, b) PureTiO2 and (c, d) 1.0-Pt-TiO2.

The exact loading contents of metal Pt for all samples were determined by ICP. For sample 0.1-Pt-TiO2, the Pt content measured was 0.1 wt%, which is close to the initial one. With increasing the initial Pt content, the corresponding measured Pt increased, such as from 0.43 wt% for 0.5-Pt-TiO2 to 0.85 wt% for 1.0-Pt-TiO2 and further to 1.46 wt% for 3.0-Pt-TiO2.

XRD patterns for TiO2 microspheres with and without Pt deposition were shown in Figure 2. Without Pt deposition, TiO2 microspheres were highly crystallized, as indicated by strong diffraction peaks. All diffraction peaks matched well with the standard diffraction data for rutile phase (JCPDS, No. 21-1276), which demonstrated the formation of a pure rutile phase for TiO2 microspheres. After Pt deposition, no significant changes were seen in XRD patterns. Based on the Scherrer formula’ calculation, the primary particle sizes for TiO2 samples with and without Pt modification were all about 6.2 nm. Therefore, Pt modification has no apparent influence on the particle size of TiO2 microspheres. Besides this, no traces of metal Pt were detected from the XRD patterns in the Pt-TiO2 series samples, regardless of Pt content. One of the primary reasons for this phenomenon is that Pt content in Pt-TiO2 samples is too low to be detected.

Figure 2: XRD patterns of the samples: (a) PureTiO2, (b) 0.1-Pt-TiO2, (c) 0.5-Pt-TiO2, (d) 1.0-Pt-TiO2, and (e) 3.0-Pt-TiO2. Vertical bars represent the standard diffraction data for bulk rutile TiO2. *represents the diffraction lines of internal standard nickel.

Further, Pt deposition has no apparent effects on the lattice structure of rutile TiO2. As indicated by structural refinements, the lattice parameters of all samples almost kept the same within the experimental errors. For instance, the lattice parameters for 3.0-Pt-TiO2 were ( ) nm and ( ), respectively, which are closer to that of ( ), ( ) of pure TiO2. Combining the analytic results of SEM and XRD, it can be concluded that the structure of rutile TiO2 microspheres remained unchanged after Pt loading.

It is well known that the premise of photocatalytic reaction is the adsorption of incidence light by catalysts. Therefore, UV-visible diffuse spectrum measurements appear to be particularly important. Figure 3 shows the UV-visible diffuse reflectance spectrum (UV-Vis DRS) of all samples prepared. PureTiO2 microspheres reflect above 90% visible light and all samples showed intense absorbance in the UV region ( ). Differently, as the content of Pt loading increases, strong plasma response was observed in the visible region. Pt deposition is thus playing a critical role in the visible light adsorption because highly dispersed Pt nanoparticles can absorb nearly all the incident light [21]. It is worth emphasizing that this absorbance of visible light does not contribute a lot to the UV-light activity likely because visible light with a low energy does not allow an efficient light excitation.

Figure 3: UV-visible diffusion reflectance spectra of TiO2 microspheres with Pt loaded.

Degradation of MO molecules is employed for the photocatalytic property evaluation of the samples. Specific degradation rate of MO molecule in the solution is monitored by examining the intensity variation of characteristic absorption peak of MO at 464 nm. As shown in Figure 4, all Pt-loaded microspheres exhibited a fast degradation of MO molecules. Particulary in the starting 30 min, all Pt-loaded microspheres showed a high removal of MO molecule beyond 67%, while less than 27% MO molecules were degraded by the pure TiO2 microspheres in this period of irradiation (Figure 4(c)). Moreover, the photocatalytic performance of 1.0-Pt-TiO2 sample is comparable with that of P25. Further, with increasing the Pt loading content, the photocatalytic activities became better, as indicated by the observation that the complete degradation time of MO became shortened from 80 min to 40 min as the loading quantity increased from 0.1 wt% to 0.85 wt%. Loading content to 0.85 wt% led to an optimum photocatalytic activity as indicated by a fast degradation of MO molecule in 40 min. However, higher Pt loading does not always mean high photocatalytic efficiency. For instance, the photocatalytic efficiency of 3.0-Pt-TiO2 was only half of that for 1.0-Pt-TiO2 in the whole photocatalytic process.

Figure 4: (a) Typical time-dependent absorption spectra of MO solution in the presence of 3.0-Pt-TiO2 under ultraviolet light irradiation; (b) as a function of irradiating time of MO solution for different samples in 90 min under UV light irradiation; (c) degradation rate for different Pt loading content of TiO2 after irradiation for 30 min under UV light with a wavelength of 254 nm irradiation. The photocatalytic performances of PureTiO2 and commercial P25-TiO2 were measured in the same conditions for comparison.

The optimized photocatalytic activities with Pt loading described above might be interpreted as follows. Firstly, loading metal Pt onto surfaces of TiO2 microspheres is beneficial for electronic transfer that decreases the recombination of photoinduced electrons and holes and thereby can greatly enhance the photoquantum efficiency. Nevertheless, too much metal Pt loadings may hinder the direct interaction between the incident light and microspheres, which leads to an incomplete excitement of photocatalysts. On the other hand, Pt nanoparticles loaded may attract holes to serve as recombination centers through recombining with electrons, which leads to a decrease in quantum efficiency [22]. As proposed in Scheme 1, metal Pt loaded was mainly deposited onto the face (110) and photogenerated electrons migrated predominantly along the direction [110] to metal Pt [20]. However, too much Pt loading led to the covering of the external surface of TiO2 microsphere with Pt nanoparticles (Scheme 1(b)), which contribute negatively to the photocatalytic activity because of the not enough direct interaction between incident light and semiconductor. Consequently, overfull Pt loading does not help to increase the photocatalytic activity. Also, the above phenomenon indicates that metal Pt loading only favored to the transfer of electrons and does not possess photocatalytic activity inherently or the activity is far less than TiO2 sample prepared in this work.

Scheme 1: Pictures illustrating the loading of Pt onto TiO2 microspheres: (a) <0.85 wt% Pt and (b) >0.85 wt% Pt.

FT-IR spectra of PureTiO2 and 1.0-Pt-TiO2 samples after MO degradation were given in Figure 5. For comparison, the FT-IR spectrum for PureTiO2 microspheres was also shown. The surface chemistry of the microspheres is characterized by a band observed around 1625 cm−1 for the H–O flexural vibration [23] and the bands centered at 1250 and 1155 cm−1 for the vibrations of –C–O– bonds. The lattice nature for the microspheres is represented by the bands observed between 700 and 500 cm−1 for the stretching bending vibrations of TiO2, the band around 500 cm−1 for the stretching vibration of Ti–O–Ti, and that around 600 cm−1 for bending vibration band of Ti–O and O–Ti–O. It is striking that some new weak bands appeared at 1250 and 1155 cm−1 for both PureTiO2 and 1.0-Pt-TiO2 after photocatalytic reaction, which are not observed before the photocatalytic reaction as for PureTiO2. These new bands are probably due to the residual segments of the organic molecules degraded. Moreover, the vibration signals of these new bands for PureTiO2 sample are stronger than those for 1.0-Pt-TiO2 sample, which indicates that the adsorbed residual organic pieces after MO degradation by PureTiO2 are much more. Therefore, Pt loading is in favor of the complete degradation of organic molecules.

Figure 5: FT-IR spectra for given samples: (a) PureTiO2 sample after photocatalytic reaction; (b) 1.0-Pt-TiO2 sample after photocatalytic reaction; (c) PureTiO2 sample before photocatalytic reaction.

Based on the previous experimental results, one can see that loading metal Pt onto TiO2 microspheres greatly improved the photocatalytic efficiency. This finding can be explained in terms of the special assembly structure of TiO2 microspheres and the interfacial interactions between metal Pt and microspheres. As shown in Scheme 2, excitement of microspheres by ultraviolet light leads to the separation of photogenerated electron-hole pairs. Since the work function of metal Pt is  eV, larger than that of 4.2 eV for the face (110) of TiO2 [24], the Femi energy level for microspheres locates above that of metal Pt. Therefore, electrons can easily transfer from the conduction band of TiO2 to metal Pt. Continuous transfer of electrons leads to the formation of Schottky barriers at the interfaces between Pt and TiO2 microspheres. Due to the existence of Schottky barriers [7], reverse process for electrons migration from metal Pt to TiO2 is hard to occur. Therefore, recombination of photogenerated electrons and holes can be efficiently inhibited and photoquantum efficiency increased spontaneously.

Scheme 2: Reaction mechanism proposed for the photocatalytic removal of MO molecules.

It is well known that the separation of light-induced electron-hole pairs is critical in the photocatalytic reaction. However, some photochemical processes except for the enhancement of photoquantum efficiency are hardly discussed. For example, the highly efficient utility of photogenerated electrons and holes in photo-degradation process plays an important role in enhancing the photocatalytic efficiency. In our recent work, self-assembled TiO2 microspheres sample has been found to exhibit a giant dielectric property [25], which is closely related to the cavities structure in between the parallel adjacent nanowires within the microspheres that can be taken as microcapacitors. These microcapacitors possess a giant dielectric constant and therefore might provide a superior electronic storage capacity. Because the production of light-induced electrons is faster than the degradation of MO molecule in photocatalytic reaction, compensating the time difference of photogenerated electrons and degradation reaction participated by electrons is pretty necessary. Due to the existences of microcapacitors, the accumulation and releasing of electrons can enhance the utility of electrons, while avoiding the recombination of electrons and holes. Therefore, dual roles from Pt deposition and special structure of TiO2 microspheres contribute to the efficient separation of light-induced electrons and holes that greatly enhances the utility of electrons in favor of the optimum photocatalytic activities.

4. Conclusions

We have fabricated the Pt-TiO2 microspheres by a solution chemistry with a subsequent Pt loading through a photoreduction. Pt loading led to an efficient separation of photogenerated electron-hole pairs. Meanwhile, electrons stored in the “microcapacitor” of TiO2 microspheres contributed to the enhancement of photocatalytic activity under UV light irradiation. Varying the Pt loading content gives rise to an optimum catalytic efficiency. By monitoring the surface chemistry of Pt-TiO2 microspheres before and after photocatalytic reactions, we found that the degradation of MO molecules was more complete in the presence of Pt loading.


This work was financially supported by NSFC (no. 20773132, 20771101), National Basic Research Program of China (2007CB613306), and Directional program CAS (KJCXZ–YWM05). The authors declare no conflict of interest.


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