教授
博士生导师
硕士生导师
教师拼音名称:zhuxiaodong
电子邮箱:
职称:教授
毕业院校:哈尔滨工业大学
学术荣誉:2019 当选:省高端人才
邮箱:
2019-09-26 泰山学者青年专家
2009-01-06 “国防科技创新团队”核心成员
2007-05-15 黑龙江省优秀毕业生(博士)
2007-06-30 哈尔滨工业大学优秀毕业生
最后更新时间:..
关键字:DOPED POROUS CARBON; BIFUNCTIONAL ELECTROCATALYST; EFFICIENT; NITROGEN; CARBIDE; CATHODE; FOAM; MO2C; FILM
摘要:An efficient and durable free-standing electrocatalyst is the key to achieving pH-universal hydrogen evolution reaction under ultra-high current density. Herein, the free-standing three-stage concentric shaft structure of MoC@C shell-supported MoC nanoparticles anchored Ni@N-doped carbon nanotube vertical nanoarrays (P-MoC/Ni@NCNTs-MoC@C) are fabricated through a simple spraying and pyrolysis process. The formation of a MoC@C shell facilitates Ni nanoparticles' anchoring, resulting in Ni@N-doped carbon nanotube vertical arrays (Ni@NCNTs). Additionally, the Ni@NCNTs effectively capture the escaped molybdenum vapor, leading to the generation of MoC nanoparticles. The unique structure provides increased catalytic active sites and larger specific surface area, improving charge transfer and the release of bubbles. As such, the free-standing P-MoC/Ni@NCNTs-MoC@C catalyst exhibits lower overpotentials compared to previously reported articles, with values of 238.1 mV in 1.0 M KOH (1800 mA cm-2), 250.2 mV in 0.5 M H2SO4 (1800 mA cm-2), and 567.9 mV in 1.0 M PBS (1000 mA cm-2). Additionally, it represents low Tafel slopes of 71.1 mV dec-1, 67.4 mV dec-1, and 130.3 mV dec-1 in alkaline, acidic, and neutral condition, respectively. The current work may provide insight into the rational design of free-standing catalysts for practical applications. Free-standing multi-hierarchical MoC@C shell-supported P-MoC/Ni@NCNT nanoarrays for pH-universal hydrogen evolution reaction at ultra-high current density.
卷号:12
期号:3
是否译文:否