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
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.