2018年11月17日南洋理工大学范红金教授学术报告会
通讯员: 发布时间:2018-11-15 浏览量:次
报告题目:Nano Array Electrocatalysts: Doping Engineering and Plasma-Assisted Surface Functionalization
报告人:Hong Jin Fan(School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore.)
邀请人:王双印
报告时间:2018年11月17日(星期六)上午9:30
报告地点:新化工楼B106
范红金,1999年吉林大学物理系学士,2003年新加坡国立大学物理系博士,其后分别在德国马普研究所和英国剑桥大学从事博士后,2008年加入南洋理工大学任教至今。
主要研究领域是纳米材料在能源中的应用,包括储能电池材料和电催化,少量染指低维半导体的发光现象。 目前,发表文章200多篇,其中39篇被标定为“ISI 高引论文”, H因子为72。2016 - 2018 连续三年被web of science评为材料类“高被引”作者。英国皇家化学会会员 (FSRC)。担任10个国际期刊编委成员。
Water electrolysis, fuel cells, and metal-air batteries all require efficient and cheap electrocatalysts that can significantly lower the overpotentials. Bimetallic alloys and their oxides or nitrides compounds are particularly interesting as non-precious metal electrocatalyst materials for HER and OER applications, because of their tailorable electronic structure, conductivity, and surface chemistry. Our group has been actively working on nanoarray materials directly grown on conductive substrates as electrodes for supercapacitor, batteries and electrocatalyst.
In this talk, I will present two main results about surface and interface engineering/functionalization of electrocatalysts: (1) RF nitrogen and carbon plasma as a highly effective technique for conversion reaction and surface functionalization of nanostructured electrocatalysts. The N plasma treatment not only generates hierarchical nanostructure surface, but also induces N doping as well as hydrophilicity. Using C-plasma, we can not only reduce the metal oxide surface, but also deposit a thin and uniform carbon coating. In addition, in the presence of metal catalyst, it can also generate vertical graphene nanosheets directly on electrode materials. (2) We demonstrate that dual cation doping, or cation-anion co-doping in nanoarray electrode materials can simultaneously modulate increase active sites exposure, and regulate water dissociation and hydrogen adsorption free energy). As a consequence, the dopings lead to a significant enhancement in catalytic activities for both HER and OER.