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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
Dendritic core-shell nickel-iron-copper metal/metal oxide electrode for efficient electrocatalytic water oxidation
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论文类型:期刊论文
发表时间:2018-01-26
发表刊物:NATURE COMMUNICATIONS
收录刊物:SCIE、ESI高被引论文、Scopus
卷号:9
期号:1
ISSN号:2041-1723
关键字:copper; iron; metal oxide; nickel; oxygen; water, alloy; catalyst; chemical reaction; efficiency measurement; electrochemical method; electrode; hydrogen; oxidation; oxide; reaction kinetics, Article; catalysis; catalyst; current density; cyclic potentiometry; electrochemistry; oxidation; oxygen evolution; precursor; scanning electron microscopy; surface area; synthesis; transmission electron microscopy; X ray absorption spectroscopy; X ray photoelectron spectroscopy
摘要:Electrochemical water splitting requires efficient water oxidation catalysts to accelerate the sluggish kinetics of water oxidation reaction. Here, we report a promisingly dendritic core-shell nickel-iron-copper metal/metal oxide electrode, prepared via dealloying with an electrodeposited nickel-iron-copper alloy as a precursor, as the catalyst for water oxidation. The as-prepared core-shell nickel-iron-copper electrode is characterized with porous oxide shells and metallic cores. This tri-metal-based core-shell nickel-iron-copper electrode exhibits a remarkable activity toward water oxidation in alkaline medium with an overpotential of only 180 mV at a current density of 10 mA cm(-2). The core-shell NiFeCu electrode exhibits pH-dependent oxygen evolution reaction activity on the reversible hydrogen electrode scale, suggesting that non-concerted proton-electron transfers participate in catalyzing the oxygen evolution reaction. To the best of our knowledge, the as-fabricated core-shell nickel-iron-copper is one of the most promising oxygen evolution catalysts.
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