Sulfur/Gadolinium-Codoped TiO<sub>2</sub> Nanoparticles for Enhanced Visible-Light Photocatalytic Performance

Agorku, Eric S.; Mamba, Bhekie B.; Pandey, Avinash C.; Mishra, Ajay K.

doi:https://doi.org/10.1155/2014/289150

Journal of Nanomaterials

On this page

Abstract Introduction Results Conclusions Acknowledgments References Copyright Related Articles

Research Article Corrigendum

!

A Corrigendum for this article has been published. To view the article details, please click the ‘Corrigendum’ tab above.

Special Issue

Nanomaterials and the Environment

View this Special Issue

Research Article | Open Access

Volume 2014 | Article ID 289150 | https://doi.org/10.1155/2014/289150

Sulfur/Gadolinium-Codoped TiO₂ Nanoparticles for Enhanced Visible-Light Photocatalytic Performance

Eric S. Agorku,¹Bhekie B. Mamba,¹Avinash C. Pandey,²and Ajay K. Mishra¹

Academic Editor: Godwin Ayoko

Received04 Oct 2013

Revised20 Nov 2013

Accepted04 Dec 2013

Published06 Apr 2014

Abstract

A series of S/Gd³⁺-codoped TiO₂ photocatalysts were synthesized by a modified sol-gel method. The materials were characterized by X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), UV-visible diffuse reflectance spectroscopy, scanning electron microscopy (SEM)/energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM)/energy-dispersive spectroscopy (EDS). Laboratory experiments with Indigo Carmine chosen as a model for organic pollutants were used to evaluate the photocatalytic performance of S/Gd³⁺-codoped TiO₂ under visible-light with varying concentrations of Gd³⁺ ions in the host material. XRD and Raman results confirmed the existence of anatase phase TiO₂ with particle size ranging from 5 to 12 nm. Codoping has exerted a great influence on the optical responses along with red shift in the absorption edge. S/Gd³⁺-codoped TiO₂ showed significant visible-light induced photocatalytic activity towards Indigo Carmine dye compared with S-TiO₂ or commercial TiO₂. TiO₂-S/Gd³⁺ (0.6% Gd³⁺) degraded the dye ( = 5.6 × 10⁻² min⁻¹) completely in 50 min.

1. Introduction

Recent advances in nanotechnology have shown significant interest in the study of semiconductor nanocrystals owing to their unique electronic and optical properties due to quantum confinement effect [1–5]. Semiconductors have attracted much attention in the past few decades due to their unique photocatalytic, magnetic, and optical properties. They have been widely used in solar energy applications, such as photovoltaic, photochemical, and photocatalytic remediation [6, 7]. Photocatalytic activities of semiconducting inorganic solids have attracted passionate research interest in the past few years, where their potential use as catalysts for photodegradation of toxic organic pollutants in water has been fully or partially investigated [8–10]. Semiconductors (such as TiO₂, ZnO, Fe₂O₃, CdS, and ZnS), which are characterized by filled valence band and empty conduction band [11], are proved to be important materials due to the electronic structure of the metal atom in chemical combination.

Nowadays scientific and engineering interest in TiO₂ semiconductor have received much attention owing to its high photocatalytic activity, strong oxidizing power, low cost, chemical and thermal stability, resistance to photocorrosion and nontoxicity, and its favorable optoelectronic property [12]. However, the wide band gap (anatase: 3.2 eV, rutile: 3.0 eV) limits its photocatalytic efficiency. Even though the anatase is known to be the most reactive phase of TiO₂ than the rutile crystalline phase, it has low quantum yield for oxidation steps (~5%) as a result of rapid recombination of photogenerated electron-hole pairs [13]. The high intrinsic band gap of pure TiO₂ operates effectively as a photocatalyst in the UV region of the electromagnetic spectrum. Thus, pure TiO₂ is able to use only around 4% of terrestrial solar spectrum because of its wide band gap [14]. In order to harness the full potential of the sunlight in photocatalysis, various methods, such as sensitization [15, 16], composite semiconductor coupling [17, 18], and doping of TiO₂ [19, 20], have been developed to overcome this challenge.

Nonmetal doping as an alternative for improving the visible light response of TiO₂ has been employed [21–23], and extensive research work has been done on synthesis of N-doped, C-doped, S-doped, and F-doped TiO₂ [24–27]. The doping of nonmetal could narrow the band gap by modifying the electronic structure around the conduction band of TiO₂. Theoretical calculation has shown that band gap narrowing originates from the electronic perturbations caused by the change of lattice parameters and/or by the presence of the trapped states within conduction and valence bands of TiO₂ [28–34].

Many of the recent efforts and strategies revealed that codoping of TiO₂ with a metal and nonmetal can result in the development of a highly efficient visible light active photocatalyst [35–37]. A series of studies reported the characteristic behavior of visible-active metal-doped semiconductor photocatalysts, including noble metals [38], rare earth metals [39], and transition metals [40]. Several rare earth metal ions such as La³⁺, Eu³⁺, Nd³⁺, and Ce³⁺, when doped in TiO₂, showed considerable shift of absorption towards visible region [41–44]. Additionally, lanthanide ions have the aptitude to form complexes with a variety of organic pollutants by the interaction of functional groups with f-orbitals of the lanthanides. This could provide a way to concentrate organic pollutants at the semiconductor surface [45].

Intrigued by these observations, we synthesized highly efficient visible light active S/Gd³⁺-codoped TiO₂ nanoparticles by modified sol-gel method. The preparation of S/Gd³⁺-codoped TiO₂ was optimized by varying the amount of Gd³⁺ to obtain an effective photocatalyst. The catalysts exhibited a higher visible light photocatalytic activity towards the degradation of Indigo Carmine (IC) in aqueous solution.

2. Experimental Details

All chemicals used were of analytical grade and used without further treatment. Titanium (IV) isopropoxide, Ti(OC₃H₇)₄ (97%), Indigo Carmine, gadolinium (III) nitrate hexahydrate (Gd(NO₃)₃·6H₂O), titanium (IV) oxide (product number 634662, 99.5%, <100 nm), and 2-propanol, C₃H₈O (99.8%) were purchased from Sigma Aldrich, Germany. Thiourea, CS(NH₃)₂ (99%) was purchased from Hopkin and Williams Ltd., England.

2.1. Sample Preparation

S/Gd³⁺-codoped TiO₂ was prepared by adding titanium isopropoxide (10 mL) to 2-propanol (50 mL) slowly and the mixture stirred for 30 min. A calculated amount of gadolinium (III) nitrate hexahydrate was dissolved in DI water (2 mL) and added to the mixture to give Gd : Ti of 0.2–1.0% and the mixture was further stirred for 1 h. Then thiourea (3.0 g), dissolved in DI water (5 mL), was added slowly with vigorous stirring for 2 h. The resulting mixture was dried in air in an oven at 100°C for 12 h and calcined at 500°C for 2 h. TiO₂-S/Gd³⁺ (0.0% Gd³⁺) sample was prepared in a similar manner without gadolinium (III) nitrate hexahydrate.

2.2. Evaluation of Photocatalytic Activity

The photocatalytic activity of the materials was evaluated through a suspension of 100 mg of the catalyst in 100 mL of aqueous solution of Indigo Carmine (20 mg/L) that was kept under magnetic stirring and visible light irradiation filtered using dichroic UV filter ( nm). A 150 W tungsten filament (Eurolux), kept at a distance of 11 cm from the reaction vessel, was employed as a source of radiation. The samples were magnetically stirred in the dark for 1 h prior to illumination to allow for adsorption equilibrium. Aliquots of the suspension (5 mL) were withdrawn at periodic time intervals using disposable syringe and filtered through 0.4 μm PVDF membrane filter at 30 min intervals for 4 hrs. The concentration of the Indigo Carmine remaining after illumination in the supernatant solution was determined using a Shimadzu UV-2450 spectrophotometer at nm. The photodegradation performance of the process was assessed in terms of decolorization efficiencies and kinetic studies.

2.3. Characterization

X-ray diffraction (XRD) measurements were performed on X-ray diffractometer (Rigaku Ultima IV) at 40 kV and 30 mA with Cu Kα radiation () and K-beta filter. Measurements were performed using a scintillation counter in the range of 5–90 deg at a speed of 2.0 deg/min. FT-IR spectra of the samples were recorded on PerkinElmer FT-IR spectrometer (Spectrum 100). Raman spectra of the samples were measured on PerkinElmer Raman microscope (Raman Micro 200). Optical properties were investigated using UV-vis absorption and UV-vis diffuse reflectance spectroscopy on a Shimadzu UV-2540 (Japan). BaSO₄ was used as the reflectance standard. Scanning electron microscopy (SEM) studies were obtained on a TESCAN (Vega 3 XMU) to observe the surface morphology of the powders and high resolution transmission electron spectroscopy (HRTEM) analysis was performed on a JEOL field emission electron microscope (JEM-2100F) to observe the surface morphology, structure, and grain size of the nanoparticles. Energy-dispersive X-ray spectroscopy (EDX) attached to the SEM and energy-dispersive spectroscopy (EDS) attached to HRTEM were used to determine the surface elemental composition.

3. Results and Discussions

3.1. FT-IR Analysis

The FT-IR spectra provide information on the surface chemistry of the oxide nanoparticles which are usually affected by the hydration layers or organic species which are characterized by several bands as demonstrated by several studies. Figure 1 shows the FT-IR spectra of S-TiO₂ and S/Gd³⁺-codoped TiO₂ with different Gd³⁺ concentrations calcined at 500°C. The most common feature observed in all the spectra is the appearance of (i) broad bands below 1000 cm⁻¹ assignable to the Ti–O–Ti crystal vibration [46] and (ii) those in the regions between 1620–1635 cm⁻¹ and 3350–3450 cm⁻¹ both due to bending vibrations of adsorbed water molecules and stretching vibrations [47] from the hydroxyl groups, respectively. The Ti–S peaks are the broad intense peaks below 1000 cm⁻¹ [48]. The peak at around 2340 cm⁻¹, which is dominant for the S-doped sample but absent in the commercial TiO₂, may be due to out-of-phase stretching of the −N=C=O bond [49], which was left behind on the surface by incomplete decomposition of thiourea [50]. The shift to the larger wavenumbers (from ~665 to ~722 cm⁻¹) and the sharpening of the Ti–O–Ti bands may be due to gadolinium doping. There is, however, no peak centered at 1389 cm⁻¹ which is due to the bending vibrations of C–H bond in the catalyst [51] and no residual alkoxy peaks were observed indicating the absence of impurities in the samples after calcinations.

3.2. Raman Spectroscopic Analysis

Raman spectroscopy provides additional information about the anatase crystallinity. Factor group analysis shows six Raman active modes () for anatase TiO₂ [52]. In this study, pronounced vibrational modes were observed for all the samples as shown in Figure 2. All the Raman spectra measured confirmed anatase phase of TiO₂. The Raman modes can be assigned to the Raman spectra of the anatase crystal.⁴⁹: ~143 (E_g), 197 (E_g), 398 (), 515 (), and 639 cm⁻¹ (E_g). Almost all the peaks match quite well with those reported in the literature, confirming the formation of pure anatase phase. However, herein, only five pronounced bands appear probably due to overlapping of and bands. At the same time, the blue or red shift, accompanied with some bands, may be explained in terms of reduction in crystallite sizes in the doped TiO₂ samples as noted earlier by others [53]. It is worth noting that reduction in the crystallite sizes has also been confirmed by the XRD measurements mentioned below. The highly intense E_g mode is due to scattering from the (110) face and mode from the (001). There was a shift in the position of the anatase E_g mode as a result of gadolinium doping from 637 cm⁻¹ to 643 cm⁻¹ for gadolinium-doped and -undoped S-TiO₂, respectively. This shift may be ascribed to Gd₂O₃ E_g mode in the samples. There was no intense Raman band at ~333 cm⁻¹ which is as a result of symmetry vibration of the cubic Gd₂O₃ indicating the partial replacement of Ti by Gd in the TiO₂ crystal lattice. The sharp, narrow intense peaks show crystalline state and the crystallinity was not changed as a result of doping.

3.3. X-Ray Diffraction Study

The size and the crystalline phase formation were investigated by X-ray diffraction. The XRD measurements for S-TiO₂ and S/Gd³⁺-codoped TiO₂ are shown in Figure 3. All the samples show anatase phase. The diffraction patterns of the anatase S/Gd³⁺-codoped TiO₂ and S-TiO₂ powders were compared with JCPDS database. The peak positions and their relative intensities are consistent with the standard powder diffraction pattern of anatase TiO₂. XRD patterns (Figure 3) exhibited strong diffraction peaks at 25° and 48°, indicating TiO₂ in the anatase phase. All the peaks are in good agreement with the standard spectrum (JCPDS number 84-1286). The peaks at values of 25.3, 37.8, 48.1, 54.0, 55.1, 62.9, and 75.2 correspond to the (101), (004), (200), (105), (211), (204), and (215) planes, respectively. All these peaks depict the anatase signature peaks. The sharp, intense anatase peaks show an improvement in the degree of crystallinity with fewer lattice defects. The XRD patterns show that there was no second-phase peak and also that the doping was successful. Also, in S-TiO₂ system, the S atoms may be attributed to be replaced some of the oxygen atoms in the TiO₂ crystal lattice. The absence of any residual peak(s) explains the fact that there is no sulphur found on the surface of the nanocrystal. From the XRD results it can be concluded that sulphur is in a high dissolution state in the TiO₂ lattice rather than an isolated species on the surface of TiO₂. The presence of sulphur and gadolinium was, however, confirmed by elemental analysis using EDS and EDX.

The average crystalline size was estimated from Scherrer’s equation on the anatase (, 37.8, and 48.1°) diffraction peaks (the most intense peaks for each sample): where is the crystal size of the catalyst, is the X-ray wavelength (1.54056 Ǻ), is the full width at maximum (FWHM) of the diffraction peak (radian), is a constant (0.9), and is the diffraction angle at the maximum [54]. The average crystalline size of S- (, 0.4, 0.6, 0.8, and 1.0) was calculated to be between 5 and 12 nm.

3.4. TEM and SEM Study

HRTEM and SEM were used to observe the uniformity, morphology, and microstructure of the as-prepared S-TiO₂ and S/Gd³⁺-codoped TiO₂ nanoparticles calcined at 500°C. Figures 4(a) and 4(b) show a typical HRTEM and SEM image of the prepared TiO₂-S/Gd³⁺ (0.6% Gd³⁺) photocatalysts, respectively. The particles are small and nearly spherical in shape. All the samples prepared show regular morphology, regardless of S/Gd ratio. The uniform morphology, with uniform size (5–12 nm), is due to improvement in the sol-gel process which resulted in the mobilization of Ti and O homogeneity in the TiO₂ crystalline structure.

(a)

(b)

The elemental composition of the prepared samples was estimated by EDX and EDS analyses. Figures 5(a) and 5(b) show the EDX and EDS spectra of TiO₂-S/Gd³⁺ (0.6% Gd³⁺), respectively. Both spectra of the codoped TiO₂ confirm the presence of Ti, Gd, O, and S. The spectra indicate that the main components are Ti and O with low contents of Gd and S. This may be due to the formation of S/Gd³⁺-codoped TiO₂.

(a)

(b)

3.5. UV-Visible Study

The light absorption characteristics of TiO₂ usually change after doping with nonmetal doping [21–23] and metal/nonmetal codoping [35–37]. Figures 6 and 7 show a comparison of the UV-vis absorption edge and UV-vis diffuse reflectance of commercial TiO₂, S-TiO₂, and S/Gd³⁺-codoped TiO₂ (with different concentrations of Gd³⁺), respectively. The absorption spectrum of TiO₂ consists of a single broad intense absorption around 400 nm due to the charge transfer from the valence band (mainly formed by 2p orbitals of the oxide anions) to the corresponding conduction band (mainly formed by 3d t₂g orbitals of Ti⁴⁺ cation [55]. The onset of the absorption edge for pure TiO₂ at Ca. 385 nm is consistent with intrinsic band gap absorption of pure TiO₂. However, in comparison with the bulk TiO₂, the TiO₂-S (and N from incomplete decomposition of thiourea, shown in Figure 1) shows two prominent features: (i) the appearance of a new absorption shoulder around 390–500 nm and (ii) the greatly enhanced absorbance in the range of 550–750 nm. The overall visible-light absorbance increased with Gd³⁺ doping. Such red shift in absorbance in the visible-light range is partly due to the yellow characteristic colour of the S-TiO₂ and the synergistic effect of S/Gd³⁺ codoping. In addition, in order to obtain a synergistic effect between S-TiO₂ and S/Gd³⁺-codoped TiO₂, it is important to control the addition ratios of Gd, which lead to an optimum photocatalytic activity. It was obvious that the TiO₂-S/Gd³⁺ (0.6% Gd³⁺) nanoparticles exhibited the best visible-light absorption with improved band gap.

Figure 8 shows a plot of the Kubelka-Munk function, , versus wavelength based on the following Kubelka-Munk equation: where reflectance, . The plot shows a significant red shift in the absorption coefficient of the S/Gd³⁺-codoped photocatalyst. Figure 9 contains Tauc [56] plots constructed from the Kubelka-Munk data (obtained from the UV-visible diffuse reflectance) for the photocatalysts as well as for the commercial benchmark sample. The band gap energies for the various samples were calculated by plotting the values of versus the photon energy (). The band gap values are estimated from a plot of versus . The indirect band gap values are summarized in Table 1. The number depends on the nature of the electronic transition and is 1 for a direct and 1/2 for an indirect band gap for semiconductors with a crystalline structure [56].

Extrapolation of this line to the photon energy axis (Figure 9) gives the semiconductor band gap, which is a key indicator of its visible light efficiency. Commercial TiO₂ also shows an absorption edge that fits well to the energy axis. Comparing the band gap of commercial TiO₂ and the S/Gd³⁺-codoped samples, the latter shows significant reduction in the band gap with gadolinium doping. The increase in the band gap with gadolinium doping may be due to the dominance of the d-f transitions over the sp-d transitions.

3.6. Photocatalytic Activity

The visible-light activity of the as-prepared nanoparticles was evaluated for the degradation of organic pollutants in aqueous solution, using Indigo Carmine (IC) dye as the model pollutant. The optical absorption peak at 610 nm was chosen to monitor the photodegradation process. The UV-visible spectral change of 20 ppm IC as a function of irradiation time during the course of degradation by TiO₂-S/Gd³⁺ (0.6% Gd³⁺) is shown in Figure 10.

With time increasing from 0 to 50 min, the characteristic absorption band at peaks of 610 nm decreased gradually, indicating that the IC was gradually photodegraded by the catalyst. The IC was completely removed from the solution after 50 min. The percentage removal for commercial TiO₂, TiO₂-S, and S/Gd³⁺-codoped TiO₂ with different Gd³⁺ contents is shown in Table 1. The linear relationship of versus time (Figure 11) shows that the photocatalytic degradation of IC follows the pseudo-first-order kinetics: where is the normalized IC concentration, is the reaction time, and is the apparent reaction rate constant.

The value for (Table 1, Figure 12) for the TiO₂-S/Gd³⁺ (0.6% Gd³⁺) (the most efficient photocatalyst) is min⁻¹ which is about nine (9) times that of the commercial TiO₂, min⁻¹, further demonstrating that the S/Gd³⁺-codoped TiO₂ exhibits high photocatalytic efficiency. The high photocatalytic performance of the codoped TiO₂ could be assigned to a number of factors: (i) high visible-light absorption of the catalyst due to reduced band gap, (ii) the delayed electron-hole recombination due to trapping of electrons in the conduction band by Gd³⁺ orbital, (iii) efficient transfer of the charge carriers, and (iv) effective utilization of the charge carries by the reactants, as demonstrated by the UV-visible and UV-visible DRS analyses (Figures 6 and 7).

4. Conclusions

A series of S/Gd³⁺-codoped TiO₂ nanoparticles were synthesized by a modified sol-gel method. The samples were characterized by various spectroscopic and analytical techniques. XRD and Raman analysis confirm the formation of pure crystalline anatase phase TiO₂. The UV-vis and UV-vis DRS spectral analyses indicated that S/Gd³⁺-codoping causes a red shift in the absorption band, resulting in the reduction in band gaps. The synergic effect of codoping with S and Gd³⁺ is evident in the photocatalytic performance of the catalyst. The S/Gd³⁺ systems are very effective visible-light active photocatalysts for the degradation of Indigo Carmine. Highest photocatalytic activity was observed for the TiO₂-S/Gd³⁺ (0.6% Gd³⁺) sample. The enhanced photocatalytic activity was mainly attributed to the small crystallite size, intense light absorption in the visible region, and narrow band gap energy.

Conflict of Interests

The authors declare that they have no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors gratefully acknowledge the financial support from the Faculty of Science, University of Johannesburg and the National Research Fund (NRF) South Africa, and Nanotechnology and Applications Centre, University of Allahabad, Allahabad, India. The authors also wish to thank Dr. H Mittal and Dr. V. Parashar, University of Johannesburg, for their technical support.

References

R. N. Bhargava, D. Gallagher, X. Hong, and A. Nurmikko, “Optical properties of manganese-doped nanocrystals of ZnS,” Physical Review Letters, vol. 72, no. 3, pp. 416–419, 1994.
View at: Publisher Site | Google Scholar
T. Schmidt, G. Müller, L. Spanhel, K. Kerkel, and A. Forchel, “Activation of 1.54 μm Er³⁺ fluorescence in concentrated II–VI semiconductor cluster environments,” Chemistry of Materials, vol. 10, no. 1, pp. 65–71, 1998.
View at: Google Scholar
S. Sapra, A. Prakash, A. Ghangrekar, N. Periasamy, and D. D. Sarma, “Emission properties of manganese-doped ZnS nanocrystals,” The Journal of Physical Chemistry B, vol. 109, no. 5, pp. 1663–1668, 2005.
View at: Publisher Site | Google Scholar
W. Chen, J.-O. Malm, V. Zwiller, R. Wallenberg, and J.-O. Bovin, “Size dependence of Eu²⁺ fluorescence in ZnS:Eu²⁺ nanoparticles,” Journal of Applied Physics, vol. 89, no. 5, pp. 2671–2675, 2001.
View at: Publisher Site | Google Scholar
M. A. Hines and P. Guyot-Sionnest, “Synthesis and characterization of strongly luminescing ZnS-capped CdSe nanocrystals,” The Journal of Physical Chemistry, vol. 100, no. 2, pp. 468–471, 1996.
View at: Google Scholar
K. Rajeshwar, “Hydrogen generation at irradiated oxide semiconductor-solution interfaces,” Journal of Applied Electrochemistry, vol. 37, no. 7, pp. 765–787, 2007.
View at: Publisher Site | Google Scholar
K. Rajeshwar and N. R. De Tacconi, “Solution combustion synthesis of oxide semiconductors for solar energy conversion and environmental remediation,” Chemical Society Reviews, vol. 38, no. 7, pp. 1984–1998, 2009.
View at: Publisher Site | Google Scholar
X. Yang, F. Ma, K. Li et al., “Mixed phase titania nanocomposite codoped with metallic silver and vanadium oxide: New efficient photocatalyst for dye degradation,” Journal of Hazardous Materials, vol. 175, no. 1–3, pp. 429–438, 2010.
View at: Publisher Site | Google Scholar
J. Zhao, C. Chen, and W. Ma, “Photocatalytic degradation of organic pollutants under visible light irradiation,” Topics in Catalysis, vol. 35, no. 3, pp. 269–278, 2005.
View at: Publisher Site | Google Scholar
M. M. Mohamed and M. M. Al-Esaimi, “Characterization, adsorption and photocatalytic activity of vanadium-doped TiO₂ and sulfated TiO₂ (rutile) catalysts: degradation of methylene blue dye,” Journal of Molecular Catalysis A, vol. 255, no. 1-2, pp. 53–61, 2006.
View at: Publisher Site | Google Scholar
S. Chakrabarti and B. K. Dutta, “Photocatalytic degradation of model textile dyes in wastewater using ZnO as semiconductor catalyst,” Journal of Hazardous Materials, vol. 112, no. 3, pp. 269–278, 2004.
View at: Publisher Site | Google Scholar
M. M. Joshi, N. K. Labhsetwar, P. A. Mangrulkar, S. N. Tijare, S. P. Kamble, and S. S. Rayalu, “Visible light induced photoreduction of methyl orange by N-doped mesoporous titania,” Applied Catalysis A, vol. 357, no. 1, pp. 26–33, 2009.
View at: Publisher Site | Google Scholar
E. M. Rockafellow, L. K. Stewart, and W. S. Jenks, “Is sulfur-doped TiO₂ an effective visible light photocatalyst for remediation?” Applied Catalysis B, vol. 91, no. 1-2, pp. 554–562, 2009.
View at: Publisher Site | Google Scholar
N. N. Binitha, Z. Yaakob, and R. Resmi, “Influence of synthesis methods on zirconium doped titania photocatalysts,” Central European Journal of Chemistry, vol. 8, no. 1, pp. 182–187, 2010.
View at: Publisher Site | Google Scholar
J. M. Rehm, G. L. McLendon, Y. Nagasawa, K. Yoshihara, J. Moser, and M. Grätzel, “Femtosecond electron-transfer dynamics at a sensitizing dye-semiconductor (TiO₂) interface,” The Journal of Physical Chemistry, vol. 100, no. 23, pp. 9577–9578, 1996.
View at: Google Scholar
D. Chatterjee and S. Dasgupta, “Visible light induced photocatalytic degradation of organic pollutants,” Journal of Photochemistry and Photobiology C, vol. 6, no. 2-3, pp. 186–205, 2005.
View at: Publisher Site | Google Scholar
J. E. Evans, K. W. Springer, and J. Z. Zhang, “Femtosecond studies of interparticle electron transfer in a coupled CdS-TiO₂ colloidal system,” The Journal of Chemical Physics, vol. 101, no. 7, pp. 6222–6225, 1994.
View at: Google Scholar
L. Wu, J. C. Yu, and X. Fu, “Characterization and photocatalytic mechanism of nanosized CdS coupled TiO₂ nanocrystals under visible light irradiation,” Journal of Molecular Catalysis A, vol. 244, no. 1-2, pp. 25–32, 2006.
View at: Publisher Site | Google Scholar
W. Choi, A. Termin, and M. R. Hoffmann, “The role of metal ion dopants in quantum-sized TiO₂: correlation between photoreactivity and charge carrier recombination dynamics,” The Journal of Physical Chemistry, vol. 98, no. 51, pp. 13669–13679, 1994.
View at: Google Scholar
R. Asahi, T. Morikawa, T. Ohwaki, K. Aoki, and Y. Taga, “Visible-light photocatalysis in nitrogen-doped titanium oxides,” Science, vol. 293, no. 5528, pp. 269–271, 2001.
View at: Publisher Site | Google Scholar
T. Ohno, M. Akiyoshi, T. Umebayashi, K. Asai, T. Mitsui, and M. Matsumura, “Preparation of S-doped TiO₂ photocatalysts and their photocatalytic activities under visible light,” Applied Catalysis A, vol. 265, no. 1, pp. 115–121, 2004.
View at: Publisher Site | Google Scholar
Y. Cong, J. Zhang, F. Chen, and M. Anpo, “Synthesis and characterization of nitrogen-doped TiO₂ nanophotocatalyst with high visible light activity,” The Journal of Physical Chemistry C, vol. 111, no. 19, pp. 6976–6982, 2007.
View at: Publisher Site | Google Scholar
W. Ren, Z. Ai, F. Jia, L. Zhang, X. Fan, and Z. Zou, “Low temperature preparation and visible light photocatalytic activity of mesoporous carbon-doped crystalline TiO₂,” Applied Catalysis B, vol. 69, no. 3-4, pp. 138–144, 2007.
View at: Publisher Site | Google Scholar
H. Irie, Y. Watanabe, and K. Hashimoto, “Nitrogen-concentration dependence on photocatalytic activity of TiO_2−xN_x powders,” The Journal of Physical Chemistry B, vol. 107, no. 23, pp. 5483–5486, 2003.
View at: Google Scholar
T. H. Xu, C. L. Song, Y. Liu, and G. R. Han, “Band structures of TiO₂ doped with N, C and B,” Journal of Zhejiang University Science B, vol. 7, no. 4, pp. 299–306, 2006.
View at: Publisher Site | Google Scholar
D. Li, H. Haneda, N. K. Labhsetwar, S. Hishita, and N. Ohashi, “Visible-light-driven photocatalysis on fluorine-doped TiO₂ powders by the creation of surface oxygen vacancies,” Chemical Physics Letters, vol. 401, no. 4–6, pp. 579–584, 2005.
View at: Publisher Site | Google Scholar
D. Li, H. Haneda, S. Hishita, N. Ohashi, and N. K. Labhsetwar, “Fluorine-doped TiO₂ powders prepared by spray pyrolysis and their improved photocatalytic activity for decomposition of gas-phase acetaldehyde,” Journal of Fluorine Chemistry, vol. 126, no. 1, pp. 69–77, 2005.
View at: Publisher Site | Google Scholar
Y. Cui, H. Du, and L. Wen, “Origin of visible-light-induced photocatalytic properties of S-doped anatase TiO₂ by first-principles investigation,” Solid State Communications, vol. 149, no. 15-16, pp. 634–637, 2009.
View at: Publisher Site | Google Scholar
H. Sun, Y. Bai, Y. Cheng, W. Jin, and N. Xu, “Preparation and characterization of visible-light-driven carbon-sulfur-codoped TiO₂ photocatalysts,” Industrial and Engineering Chemistry Research, vol. 45, no. 14, pp. 4971–4976, 2006.
View at: Publisher Site | Google Scholar
K. Lv, H. Zuo, J. Sun et al., “(Bi, C and N) codoped TiO₂ nanoparticles,” Journal of Hazardous Materials, vol. 161, no. 1, pp. 396–401, 2009.
View at: Publisher Site | Google Scholar
H. Xu and L. Zhang, “Selective nonaqueous synthesis of C-Cl-codoped TiO₂ with visible-light photocatalytic activity,” The Journal of Physical Chemistry C, vol. 114, no. 26, pp. 11534–11541, 2010.
View at: Publisher Site | Google Scholar
Y. Cong, J. Zhang, F. Chen, M. Anpo, and D. He, “Preparation, photocatalytic activity, and mechanism of nano-TiO₂ Co-doped with nitrogen and iron (III),” The Journal of Physical Chemistry C, vol. 111, no. 28, pp. 10618–10623, 2007.
View at: Publisher Site | Google Scholar
Y. Wang, Y. Huang, W. Ho, L. Zhang, Z. Zou, and S. Lee, “Biomolecule-controlled hydrothermal synthesis of C-N-S-tridoped TiO₂ nanocrystalline photocatalysts for NO removal under simulated solar light irradiation,” Journal of Hazardous Materials, vol. 169, no. 1–3, pp. 77–87, 2009.
View at: Publisher Site | Google Scholar
P. Wang, P.-S. Yap, and T.-T. Lim, “C-N-S tridoped TiO₂ for photocatalytic degradation of tetracycline under visible-light irradiation,” Applied Catalysis A, vol. 399, no. 1-2, pp. 252–261, 2011.
View at: Publisher Site | Google Scholar
Y. Sakatani, H. Ando, K. Okusako et al., “Metal ion and N co-doped TiO₂ as a visible-light photocatalyst,” Journal of Materials Research, vol. 19, no. 7, pp. 2100–2108, 2004.
View at: Publisher Site | Google Scholar
Y. Sakatani, J. Nunoshige, H. Ando et al., “Photocatalytic decomposition of acetaldehyde under visible light irradiation over La³⁺ and N Co-doped TiO₂,” Chemistry Letters, vol. 32, no. 12, pp. 1156–1157, 2003.
View at: Google Scholar
W. Zhao, W. Ma, C. Chen, J. Zhao, and Z. Shuai, “Efficient degradation of toxic organic pollutants with Ni₂O₃/TiO_2−xB_x under visible irradiation,” Journal of the American Chemical Society, vol. 126, no. 15, pp. 4782–4783, 2004.
View at: Publisher Site | Google Scholar
U. Siemon, D. Bahnemann, J. J. Testa, D. Rodríguez, M. I. Litter, and N. Bruno, “Heterogeneous photocatalytic reactions comparing TiO₂ and Pt/TiO₂,” Journal of Photochemistry and Photobiology A, vol. 148, no. 1–3, pp. 247–255, 2002.
View at: Publisher Site | Google Scholar
A.-W. Xu, Y. Gao, and H.-Q. Liu, “The preparation, characterization, and their photocatalytic activities of rare-earth-doped TiO₂ nanoparticles,” Journal of Catalysis, vol. 207, no. 2, pp. 151–157, 2002.
View at: Publisher Site | Google Scholar
K. Wilke and H. D. Breuer, “The influence of transition metal doping on the physical and photocatalytic properties of titania,” Journal of Photochemistry and Photobiology A, vol. 121, no. 1, pp. 49–53, 1999.
View at: Google Scholar
F. B. Li, X. Z. Li, and M. F. Hou, “Photocatalytic degradation of 2-mercaptobenzothiazole in aqueous La³⁺-TiO₂ suspension for odor control,” Applied Catalysis B, vol. 48, no. 3, pp. 185–194, 2004.
View at: Publisher Site | Google Scholar
M. Zalas and M. Laniecki, “Photocatalytic hydrogen generation over lanthanides-doped titania,” Solar Energy Materials and Solar Cells, vol. 89, no. 2-3, pp. 287–296, 2005.
View at: Publisher Site | Google Scholar
Y. Wang, H. Cheng, L. Zhang et al., “The preparation, characterization, photoelectrochemical and photocatalytic properties of lanthanide metal-ion-doped TiO₂ nanoparticles,” Journal of Molecular Catalysis A, vol. 151, no. 1-2, pp. 205–216, 2000.
View at: Publisher Site | Google Scholar
Y. Xie and C. Yuan, “Visible-light responsive cerium ion modified titania sol and nanocrystallites for X-3B dye photodegradation,” Applied Catalysis B, vol. 46, no. 2, pp. 251–259, 2003.
View at: Publisher Site | Google Scholar
Y. Zhang, H. Xu, Y. Xu, H. Zhang, and Y. Wang, “The effect of lanthanide on the degradation of RB in nanocrystalline Ln/TiO₂ aqueous solution,” Journal of Photochemistry and Photobiology A, vol. 170, no. 3, pp. 279–285, 2005.
View at: Publisher Site | Google Scholar
F. Boccuzzi, A. Chiorino, S. Tsubota, and M. Haruta, “FTIR study of carbon monoxide oxidation and scrambling at room temperature over gold supported on ZnO and TiO₂,” The Journal of Physical Chemistry, vol. 100, no. 9, pp. 3625–3631, 1996.
View at: Google Scholar
P. Cheng, J. Qiu, M. Gu, Y. Jin, and W. Shangguan, “Synthesis of shape-controlled titania particles from a precursor solution containing urea,” Materials Letters, vol. 58, no. 29, pp. 3751–3755, 2004.
View at: Publisher Site | Google Scholar
H. Sun, Y. Bai, Y. Cheng, W. Jin, and N. Xu, “Preparation and characterization of visible-light-driven carbon-Sulfur-codoped TiO₂ photocatalysts,” Industrial and Engineering Chemistry Research, vol. 45, no. 14, pp. 4971–4976, 2006.
View at: Publisher Site | Google Scholar
A. T. Kuvarega, R. W. M. Krause, and B. B. Mamba, “Nitrogen/palladium-codoped TiO₂ for efficient visible light photocatalytic dye degradation,” The Journal of Physical Chemistry C, vol. 115, no. 45, pp. 22110–22120, 2011.
View at: Publisher Site | Google Scholar
L. Ren, X. Huang, F. Sun, and X. He, “Preparation and characterization of doped TiO₂ nanodandelion,” Materials Letters, vol. 61, no. 2, pp. 427–431, 2007.
View at: Publisher Site | Google Scholar
J. A. Wang, R. Limas-Ballesteros, T. López et al., “Quantitative determination of titanium lattice defects and solid-state reaction mechanism in iron-doped TiO₂ photocatalysts,” The Journal of Physical Chemistry B, vol. 105, no. 40, pp. 9692–9698, 2001.
View at: Publisher Site | Google Scholar
H. C. Choi, Y. M. Jung, and S. B. Kim, “Size effects in the Raman spectra of TiO₂ nanoparticles,” Vibrational Spectroscopy, vol. 37, no. 1, pp. 33–38, 2005.
View at: Publisher Site | Google Scholar
D. B. Hamal and K. J. Klabunde, “Synthesis, characterization, and visible light activity of new nanoparticle photocatalysts based on silver, carbon, and sulfur-doped TiO₂,” Journal of Colloid and Interface Science, vol. 311, no. 2, pp. 514–522, 2007.
View at: Publisher Site | Google Scholar
M. Yan, F. Chen, J. Zhang, and M. Anpo, “Preparation of controllable crystalline titania and study on the photocatalytic properties,” The Journal of Physical Chemistry B, vol. 109, no. 18, pp. 8673–8678, 2005.
View at: Publisher Site | Google Scholar
N. Venkatachalam, M. Palanichamy, and V. Murugesan, “Sol-gel preparation and characterization of alkaline earth metal doped nano TiO₂: efficient photocatalytic degradation of 4-chlorophenol,” Journal of Molecular Catalysis A, vol. 273, no. 1-2, pp. 177–185, 2007.
View at: Publisher Site | Google Scholar
S. Sakthivel and H. Kisch, “Daylight photocatalysis by carbon-modified titanium dioxide,” Angewandte Chemie, vol. 42, no. 40, pp. 4908–4911, 2003.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2014 Eric S. Agorku 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.

PDF Download Citation

Download other formats

Order printed copies

Views

2363

Downloads

1373

Citations