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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3D Core-Shell NiFeCr Catalyst on a Cu Nanoarray for Water Oxidation: Synergy between Structural and Electronic Modulation

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论文类型:期刊论文

发表时间:2018-12-14

发表刊物:ACS Energy Letters

卷号:3

期号:12

页面范围:2865-2874

关键字:Alkalinity; Copper; Electrocatalysts; Electronic structure; Heterojunctions; Modulation; Oxidation; Reaction kinetics; Shells (structures); Ternary alloys, Activation method; Alkaline conditions; Cr incorporations; Electron transfer; Mass-transport process; Nano-architecture; Oxygen evolution reaction; Structure activity relationships, Catalyst activity

摘要:Low-cost transition metal-based electrocatalysts for water oxidation and understanding their structure-activity relationship are greatly desired for clean and sustainable chemical fuel production. Herein, a core-shell (CS) NiFeCr metal/metal hydroxide catalyst was fabricated on a 3D Cu nanoarray by a simple electrodeposition-activation method. A synergistic promotion effect between electronic structure modulation and nanostructure regulation was presented on a CS-NiFeCr oxygen evolution reaction (OER) catalyst: the 3D nanoarchitecture facilitates the mass transport process, the in situ formed interface metal/metal hydroxide heterojunction accelerates the electron transfer, and the electronic structure modulation by Cr incorporation improves the reaction kinetics. Benefiting from the synergy between structural and electronic modulation, the catalyst shows excellent activity toward water oxidation under alkaline conditions: overpotential of 200 mV at 10 mA/cm2 current density and Tafel slope of 28 mV/dec. This work opens up a new window for understanding the structure-activity relationship of OER catalysts and encourages new strategies for development of more advanced OER catalysts. © 2018 American Chemical Society.