过电位
材料科学
塔菲尔方程
纳米线
化学工程
双金属片
钼
催化作用
纳米技术
无机化学
电极
电化学
物理化学
有机化学
冶金
金属
化学
工程类
作者
Huan Li,Minghao Hu,Luyao Zhang,Lili Huo,Jing Peng,Baocang Liu,Rui Gao,Jun Zhang,Bin Liu
标识
DOI:10.1002/adfm.202003198
摘要
Abstract An ecofriendly and robust strategy is developed to construct a self‐supported monolithic electrode composed of N‐doped carbon hybridized with bimetallic molybdenum‐tungsten carbide (Mo x W 2− x C) to form composite nanowires for hydrogen evolution reaction (HER). The hybridization of Mo x W 2− x C with N‐doped carbon enables effective regulation of the electrocatalytic performance of the composite nanowires, endowing abundant accessible active sites derived from N‐doping and Mo x W 2− x C incorporation, outstanding conductivity resulting from the N‐doped carbon matrix, and appropriate positioning of the d‐band center with a thermodynamically favorable hydrogen adsorption free energy (Δ G H* ) for efficient hydrogen evolution catalysis, which forms a binder‐free 3D self‐supported monolithic electrode with accessible nanopores, desirable chemical compositions and stable composite structure. By modulating the Mo/W ratio, the optimal Mo 1.33 W 0.67 C @ NC nanowires on carbon cloth achieve a low overpotential (at a geometric current density of 10 mA cm −2 ) of 115 and 108 mV and a small Tafel slope of 58.5 and 55.4 mV dec −1 in acidic and alkaline environments, respectively, which can maintain 40 h of stable performance, outperforming most of the reported metal‐carbide‐based HER electrocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI