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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Tailoring Active Sites in Mesoporous Defect-Rich NC/V-o-WON Heterostructure Array for Superior Electrocatalytic Hydrogen Evolution

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论文类型:期刊论文

发表时间:2019-03-27

发表刊物:ADVANCED ENERGY MATERIALS

收录刊物:SCIE、EI

卷号:9

期号:12

ISSN号:1614-6832

关键字:nanorod arrays; density functional theory; hydrogen evolution reaction; heterostructures; nitrogen-doped carbon

摘要:Tailoring active sites in earth-abundant non-noble metal electrocatalysts are required toward widespread applications in sustainable energy fields. Herein, an integrated mesoporous heterostructure array is reported by a hydrogenation/nitridation-induced in situ growth strategy. Highly conductive oxygen-vacancies-rich tungsten oxynitride (V-o-WON) nanorod array acts as the backbone encapsulated by ultrathin nitrogen-doped carbon (NC) nanolayers, forming high-quality shell/core NC/V-o-WON heterostructures. Density functional theory calculations reveal that defect-rich heterostructure arrays not only enhance the conductivity and modulate electronic structure but also promote the adsorption and dissociation of reactants and offer substantial potential sites. As expected, porous NC/V-o-WON array exhibits a small overpotential of 16 mV at the current density of 10 mA cm(-2) and a low Tafel slope of 33 mV per decade in alkaline media, accompanied by negligible loss upon a large current density over 100 h. Benefiting from outstanding electrocatalytic hydrogen evolution reaction performance and stability, this defective heterostructure could serve as a prominent alternative electrocatalyst for renewable energy applications.