塔菲尔方程
过电位
材料科学
电催化剂
分解水
催化作用
纳米团簇
化学工程
堆积
制氢
电化学
纳米技术
无机化学
物理化学
电极
化学
有机化学
光催化
工程类
作者
Xiaomei Yu,Wei Shi,Jiajiao Wei,Tiantian Liu,Yuanyuan Li,Mengyuan He,Zhengyu Wei,Dehai Ping,Panfei Sun,Jin You Zheng,Songjie Li
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2023-11-22
卷期号:35 (6): 065704-065704
标识
DOI:10.1088/1361-6528/ad0985
摘要
Abstract Developing non-noble-metal electrocatalysts for hydrogen evolution reactions with high activity and stability is the key issue in green hydrogen generation based on electrolytic water splitting. It has been recognized that the stacking of large CoP particles limits the intrinsic activity of as-synthesized CoP catalyst for hydrogen evolution reaction. In the present study, N-Mo x C/CoP-0.5 with excellent electrocatalytic activity for hydrogen evolution reaction was prepared using N-Mo x C as decoration. A reasonable overpotential of 106 mV (at 10 mA cm −2 ) and a Tafel slope of 59 mV dec −1 in 1.0 M KOH solution was achieved with N-Mo x C/CoP-0.5 electrocatalyst, which exhibits superior activity even after working for 37 h. Uniformly distributed ultrafine nanoclusters of the N-Mo x C/CoP-0.5 hybrids could provide sufficient interfaces for enhanced charge transfer. The effective capacity of the hydrogen evolution reaction could be preserved in the complex, and the enlarged electrocatalytic surface area could be expected to offer more active sites for the reaction.
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