塔菲尔方程
纳米点
MXenes公司
材料科学
介孔材料
过电位
纳米技术
二硫化钼
比表面积
化学工程
催化作用
电化学
化学
电极
有机化学
复合材料
物理化学
工程类
作者
Yi Tang,Chenhui Yang,Yangyang Xie,Yunqing Kang,Wenxiu Que,Joel Henzie,Yusuke Yamauchi
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2022-12-28
卷期号:11 (1): 168-176
被引量:6
标识
DOI:10.1021/acssuschemeng.2c05106
摘要
Two-dimensional (2D) MXene-based mesoporous heterostructures are promising electrode materials for electrochemical charge storage but have rarely been examined as electrocatalysts for hydrogen production reactions. Herein, we describe a 2D MXene-based mesoporous nanoarchitecture consisting of 2D Ti3C2 (MXene) nanosheets sandwiched between ordered mesoporous nitrogen-doped carbon (mNC) layers coupled molybdenum carbide (MoC) nanodots (denoted as mNC-MoC/Ti3C2). The results show that mesopores significantly increase the specific surface area of the material and expose numerous electrocatalytically active sites. Mesopores also shorten the distance of ion transport to the inner surface of the catalyst and accelerate the kinetics of the catalytic reaction. The resulting mNC-MoC/Ti3C2 structure exhibits excellent performance in the hydrogen evolution reaction (HER) in 0.5 M H2SO4, with a small overpotential of 159 mV at 10 mA cm–2, a low Tafel slope of 70.9 mV dec–1, and excellent long-term stability. Theoretical calculations indicate that the mNC-MoC/Ti3C2 surface has a small hydrogen binding energy for the favorable adsorption–desorption of hydrogen and high conductivity for rapid charge transfer during the HER process.
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