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Electrolyte Concentration Effect of a Photoelectrochemical Cell Consisting of Nanotube Anode

DOI: 10.1155/2013/682516

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Abstract:

The photoelectrochemical responses of a TiO2 nanotube anode in ethylene glycol (EG), glycerol, ammonia, ethanol, urea, and Na2S electrolytes with different concentrations were investigated. The TiO2 nanotube anode was highly efficient in photoelectrocatalysis in these solutions under UV light illumination. The photocurrent density is obviously affected by the concentration change. Na2S generated the highest photocurrent density at 0, 1, and 2?V bias voltages, but its concentration does not significantly affect the photocurrent density. Urea shows high open circuit voltage at proper concentration and low photocurrent at different concentrations. Externally applied bias voltage is also an important factor that changes the photoelectrochemical reaction process. In view of the open circuit voltage, EG, ammonia, and ethanol fuel cells show the trend that the open circuit voltage (OCV) increases with the increase of the concentration of the solutions. Glycerol has the highest OCV compared with others, and it deceases with the increase in the concentration because of the high viscosity. The OCV of the urea and Na2S solutions did not show obvious concentration effect. 1. Introduction Titanium dioxide (TiO2) has been widely studied because it has good photovoltaic property. Photoelectrochemical cell (PEC) is a device that could degrade pollutants, splitting water by utilizing photon energy while electric energy is generated. Clean energy generation by environmentally friend method is a very important issue. Hydrogen is used in fuel cells, but nature gas is still a main source for hydrogen production. It contains contaminative byproducts. Only a few part of hydrogen is produced by water splitting in the world [1]. Pollutant degradation is another very important application of PEC. TiO2 nanostructured anode has the high potential for clean energy production and hazard material degradation. Many hazardous organic materials can be converted into clean substances by TiO2 anode PEC, which include methylene blue [2, 3], glucose [4], organic compounds [5, 6], waste water [7], dye pollutant [8], and even CO2 [9] of the greenhouse gas. By using various electrolytes, different levels of open circuit voltage, current density, filling factor can be reached [10–12]. The bias potential and concentration of electrolytes can also influence the performance of a PEC cell. Normally, the additionally applied external bias voltage can further enhance the PEC reaction process because the conduction band edge of anode material cannot lie above the energy level. Quan et al. [13]

References

[1]  C. Carver, Z. Ulissi, C. K. Ong, S. Dennison, G. H. Kelsall, and K. Hellgardt, “Modelling and development of photoelectrochemical reactor for H2 production,” International Journal of Hydrogen Energy, vol. 37, no. 1, pp. 2911–2923, 2012.
[2]  T. C. An, X. H. Zhu, and Y. Xiong, “Feasibility study of photoelectrochemical degradation of methylene blue with three-dimensional electrode-photocatalytic reactor,” Chemosphere, vol. 46, no. 6, pp. 897–903, 2002.
[3]  G. Li, H. Y. Yip, K. H. Wong, C. Hu, J. Qu, and P. K. Wong, “Photoelectrochemical degradation of Methylene Blue with β-PbO2 electrodes driven by visible light irradiation,” Journal of Environmental Sciences, vol. 23, no. 6, pp. 998–1003, 2011.
[4]  B. C. Liu, J. H. Li, B. X. Zhou et al., “Kinetics and mechanisms for photoelectrochemical degradation of glucose on highly effective self-organized TiO2 nanotube arrays,” Chinese Journal of Catalysis, vol. 31, no. 2, pp. 163–170, 2010.
[5]  H. Zhao, D. Jiang, S. Zhang, and W. Wen, “Photoelectrocatalytic oxidation of organic compounds at nanoporous TiO2 electrodes in a thin-layer photoelectrochemical cell,” Journal of Catalysis, vol. 250, no. 1, pp. 102–109, 2007.
[6]  M. Antoniadou and P. Lianos, “Near Ultraviolet and Visible light photoelectrochemical degradation of organic substances producing electricity and hydrogen,” Journal of Photochemistry and Photobiology A, vol. 204, no. 1, pp. 69–74, 2009.
[7]  S. Zhang, L. Li, H. Zhao, and G. Li, “A portable miniature UV-LED-based photoelectrochemical system for determination of chemical oxygen demand in wastewater,” Sensors and Actuators B, vol. 141, no. 2, pp. 634–640, 2009.
[8]  C. Kim, J. T. Kim, K. S. Kim, S. Jeong, H. Y. Kim, and Y. S. Han, “Immobilization of TiO2 on an ITO substrate to facilitate the photoelectrochemical degradation of an organic dye pollutant,” Electrochimica Acta, vol. 54, no. 24, pp. 5715–5720, 2009.
[9]  Y. P. Peng, Y. T. Yeh, S. I. Shah, and C. P. Huang, “Concurrent photoelectrochemical reduction of CO2 and oxidation of methyl orange using nitrogen-doped TiO2,” Applied Catalysis B, vol. 123-124, no. 1, pp. 414–423, 2012.
[10]  M. Kaneko, J. Nemoto, H. Ueno et al., “Photoelectrochemical reaction of biomass and bio-related compounds with nanoporous TiO2 film photoanode and O2-reducing cathode,” Electrochemistry Communications, vol. 8, no. 2, pp. 336–340, 2006.
[11]  Y. Liu, J. Li, B. Zhou et al., “Efficient electricity production and simultaneously wastewater treatment via a high-performance photocatalytic fuel cell,” Water Research, vol. 45, no. 13, pp. 3991–3998, 2011.
[12]  Y. X. Gan, B. J. Gan, E. Clark, L. Su, and L. Zhang, “Converting environmentally hazardous materials into clean energy using a novel nanostructured photoelectrochemical fuel cell,” Materials Research Bulletin, vol. 47, no. 9, pp. 2380–2388, 2012.
[13]  X. Quan, X. Ruan, H. Zhao, S. Chen, and Y. Zhao, “Photoelectrocatalytic degradation of pentachlorophenol in aqueous solution using a TiO2 nanotube film electrode,” Environmental Pollution, vol. 147, no. 2, pp. 409–414, 2007.
[14]  S. Zhang, H. Zhao, D. Jiang, and R. John, “Photoelectrochemical determination of chemical oxygen demand based on an exhaustive degradation model in a thin-layer cell,” Analytica Chimica Acta, vol. 514, no. 1, pp. 89–97, 2004.
[15]  V. M. Nikale, S. S. Shinde, A. R. Babar, C. H. Bhosale, and K. Y. Rajpure, “Photoelectrochemical performance of sprayed n-CdIn2Se4 photoanodes,” Solar Energy, vol. 85, no. 2, pp. 325–333, 2011.
[16]  S. Zhang, W. Wen, D. Jiang et al., “Photoelectrochemical characterisation of TiO2 thin films derived from microwave hydrothermally processed nanocrystalline colloids,” Journal of Photochemistry and Photobiology A, vol. 179, no. 3, pp. 305–313, 2006.
[17]  G. Milczarek, A. Kasuya, S. Mamykin, T. Arai, K. Shinoda, and K. Tohji, “Optimization of a two-compartment photoelectrochemical cell for solar hydrogen production,” International Journal of Hydrogen Energy, vol. 28, no. 9, pp. 919–926, 2003.
[18]  F. Hao, H. Lin, J. Zhang, D. Zhuang, Y. Liu, and J. Li, “Influence of iodine concentration on the photoelectrochemical performance of dye-sensitized solar cells containing non-volatile electrolyte,” Electrochimica Acta, vol. 55, no. 24, pp. 7225–7229, 2010.
[19]  P. Lianos, “Production of electricity and hydrogen by photocatalytic degradation of organic wastes in a photoelectrochemical cell. The concept of the Photofuelcell: a review of a re-emerging research field,” Journal of Hazardous Materials, vol. 185, no. 2-3, pp. 575–590, 2011.

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