Oxidative energy storage behavior of a porous nanostructured TiO2-Ni(OH)(2) bilayer photocatalysis system | |
Lian, Hui-Qin2; Wang, Jian-Ming2; Xu, Lei2; Zhang, Li-Ying2; Shao, Hai-Bo2; Zhang, Jian-Qing1,2; Cao, Chu-Nan1,2 | |
刊名 | ELECTROCHIMICA ACTA
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2011-02-01 | |
卷号 | 56期号:5页码:2074-2080 |
关键词 | Energy storage TiO2-Ni(OH)(2) bilayer Oxidation of Ni(OH)(2) Photoelectrochemical behavior |
ISSN号 | 0013-4686 |
DOI | 10.1016/j.electacta.2010.11.097 |
通讯作者 | Wang, Jian-Ming(wjm@zju.edu.cn) |
英文摘要 | TiO2-Ni(OH)(2) bilayer electrodes were prepared by the cathodic electrodeposition of Ni(OH)(2) layer on a TiO2/ITO substrate. The porous Ni(OH)(2) layers were obtained at relatively high current densities (>= 1.0 mA cm(-2)), and the particle size increased with increasing the deposition current density. A porous nanostructured TiO2-Ni(OH)(2) bilayer was obtained at a current density of 1.0 mA cm(-2). The effects of OH- concentration in the electrolyte and surface structure in the Ni(OH)(2) layer on storage of the oxidative energy of TiO2 were investigated. In our experimental conditions the oxidative energy storage of an UV-irradiated TiO2 photocatalyst in Ni(OH)(2) was obviously enhanced in the electrolyte with 1.0 M OH-. The porous nanostructured TiO2-Ni(OH)(2) bilayer electrode showed the notably improved oxidative energy storage performance, resulting from its porous structure and nanostructured Ni(OH)(2) particles. The TiO2-Ni(OH)(2) bilayer electrode during UV irradiation exhibited much higher potentials and larger photocurrent than the TiO2/ITO electrode. The transition from Ni(OH)(2) to NiOOH under UV irradiation proceeded in the potential range of -0.5 to -0.2 V. much more negative than the Ni(OH)(2)/NiOOH redox potential. A possible mechanism on the oxidative energy storage of an UV-irradiated TiO2 photocatalyst in Ni(OH)(2) was proposed, and the related experimental results were discussed in terms of the suggested model. (C) 2010 Elsevier Ltd. All rights reserved. |
资助项目 | National Natural Science Foundation of China[50972128] |
WOS研究方向 | Electrochemistry |
语种 | 英语 |
出版者 | PERGAMON-ELSEVIER SCIENCE LTD |
WOS记录号 | WOS:000288227800023 |
资助机构 | National Natural Science Foundation of China |
内容类型 | 期刊论文 |
源URL | [http://ir.imr.ac.cn/handle/321006/107046] ![]() |
专题 | 金属研究所_中国科学院金属研究所 |
通讯作者 | Wang, Jian-Ming |
作者单位 | 1.Chinese Acad Sci, Inst Met Res, State Key Lab Corros & Protect Met, Shenyang 110016, Peoples R China 2.Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China |
推荐引用方式 GB/T 7714 | Lian, Hui-Qin,Wang, Jian-Ming,Xu, Lei,et al. Oxidative energy storage behavior of a porous nanostructured TiO2-Ni(OH)(2) bilayer photocatalysis system[J]. ELECTROCHIMICA ACTA,2011,56(5):2074-2080. |
APA | Lian, Hui-Qin.,Wang, Jian-Ming.,Xu, Lei.,Zhang, Li-Ying.,Shao, Hai-Bo.,...&Cao, Chu-Nan.(2011).Oxidative energy storage behavior of a porous nanostructured TiO2-Ni(OH)(2) bilayer photocatalysis system.ELECTROCHIMICA ACTA,56(5),2074-2080. |
MLA | Lian, Hui-Qin,et al."Oxidative energy storage behavior of a porous nanostructured TiO2-Ni(OH)(2) bilayer photocatalysis system".ELECTROCHIMICA ACTA 56.5(2011):2074-2080. |
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