Citation: SHANGGUAN Peng-Peng, TONG Shao-Ping, LI Hai-Li, LENG Wen-Hua. Influence of the Potential on the Charge-Transfer Rate Constant of Photooxidation of Water over α-Fe₂O₃ and Ti-Doped α-Fe₂O₃[J]. Acta Physico-Chimica Sinica, ;2013, 29(09): 1954-1960. doi: 10.3866/PKU.WHXB201306261 shu

Influence of the Potential on the Charge-Transfer Rate Constant of Photooxidation of Water over α-Fe₂O₃ and Ti-Doped α-Fe₂O₃

1.
1 College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310032, P. R. China;
2 Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China

Received Date: 22 April 2013
Available Online: 26 June 2013
Fund Project: 国家重点基础研究发展规划项目(973)(2011CB936003) (973)(2011CB936003)国家自然科学基金(50971116)资助 (50971116)

It has been reported that applying a certain external anodic potential over un-doped (α-Fe₂O₃) and Ti-doped α-Fe₂O₃ (Ti-Fe₂O₃) electrodes can improve the photocurrent or the photoelectrochemical oxidation rate of water. However, it is assumed in the literature that the potential drops completely across the side of the solid semiconductor (band edge pinning), and the influence of the potential on the interfacial charge-transfer rate constant is rarely reported. In this article, the impact of the applied potential on the interfacial charge-transfer rate constant during photoelectrochemical oxidation of water over the two electrodes was investigated by electrochemical impedance spectroscopy. The results showed that by increasing the applied anodic potential, the interfacial charge-transfer rate constants for both electrodes were increased. The smaller increase in the magnitude of the rate constant than determined by theory indicates that not all of the applied potential drops across the Helmholtz layer, but takes place in both the space charge and Helmholtz layers simultaneously (Fermi level pinning). The results of the surface-state capacitance measurements suggested that the photo-generated charge can be accumulated in the surface states, resulting in the re-distribution of the potential at the interface and an improvement in the rate constant. Under the same applied potential, the higher the light intensity is, the more the photogenerated holes accumulated in the surface states. This causes an increase in the potential drop across the Helmholtz layer and consequently increases the charge-transfer rate constant. Compared with the α-Fe₂O₃, the improvement of the charge-transfer rate constant by the anodic potential is more obvious.
- α-Fe₂O₃,
- Ti-doped α-Fe₂O₃,
- Photoelectrochemical oxidation of water,
- Potential distribution,
- Electrochemical impedance spectroscopy,
- Photoelectrochemistry
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通讯作者: 陈斌, bchen63@163.com

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沈阳化工大学材料科学与工程学院沈阳 110142

Influence of the Potential on the Charge-Transfer Rate Constant of Photooxidation of Water over α-Fe2O3 and Ti-Doped α-Fe2O3

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通讯作者: 陈斌, bchen63@163.com

Influence of the Potential on the Charge-Transfer Rate Constant of Photooxidation of Water over α-Fe₂O₃ and Ti-Doped α-Fe₂O₃