孙立成

个人信息Personal Information

教授

博士生导师

硕士生导师

主要任职:无

其他任职:精细化工国家重点实验室副主任、大连理工大学-瑞典皇家工学院分子器件联合研究中心主任

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:应用化学. 精细化工

办公地点:大连理工大学西部校区化工实验楼E-223

联系方式:0411-84986493

电子邮箱:sunlc@dlut.edu.cn

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In Situ Formation of Efficient Cobalt-Based Water Oxidation Catalysts from Co2+-Containing Tungstate and Molybdate Solutions

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论文类型:期刊论文

发表时间:2015-10-01

发表刊物:CHEMISTRY-AN ASIAN JOURNAL

收录刊物:SCIE、EI、PubMed、Scopus

卷号:10

期号:10,SI

页面范围:2228-2233

ISSN号:1861-4728

关键字:cobalt; heterogeneous catalysis; molybdenum; tungsten; water splitting

摘要:Replacing rare and expensive noble-metal catalysts with inexpensive and earth-abundant ones is of great importance to split water either electrochemically or photo-electrochemically. In this study, two amorphous cobalt oxide catalysts (Co-W film and Co-Mo film) with high activity for electrocatalytic water oxidation were prepared by fast, simple electrodeposition from aqueous solutions of Na2WO4 and Na2MoO4 containing Co2+. In solutions of Na2WO4 and Na2MoO4, sustained anodic current densities up to 1.45 and 0.95 mAcm(-2) were obtained for Co-W film at 1.87 V versus a reversible hydrogen electrode (RHE) and Co-Mo film on fluorine-doped tin oxide (FTO) substrates at 1.85V versus RHE. For the Co-W film, a much higher current density of 4.5 mAcm(-2) was acquired by using a stainless-steel mesh as the electrode substrate. Significantly, in long-term electrolysis for 13 h, the Co-W film exhibited improved stability in cobalt-free buffer solution in comparison with the previously reported Co-Pi film.