中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Oxidative energy storage behavior of a porous nanostructured TiO2-Ni(OH)(2) bilayer photocatalysis system

文献类型:期刊论文

作者Lian, Hui-Qin1; Wang, Jian-Ming1; Xu, Lei1; Zhang, Li-Ying1; Shao, Hai-Bo1; Zhang, Jian-Qing1,2; Cao, Chu-Nan1,2
刊名ELECTROCHIMICA ACTA
出版日期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
DOI10.1016/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
WOS记录号WOS:000288227800023
出版者PERGAMON-ELSEVIER SCIENCE LTD
资助机构National Natural Science Foundation of China
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.Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
2.Chinese Acad Sci, Inst Met Res, State Key Lab Corros & Protect Met, Shenyang 110016, 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.

入库方式: OAI收割

来源:金属研究所

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