过电位
双金属片
分解水
析氧
材料科学
双功能
法拉第效率
电解水
化学工程
纳米颗粒
电解
纳米技术
催化作用
电化学
化学
电极
物理化学
电解质
金属
冶金
光催化
有机化学
工程类
作者
Jinxu Zhang,Xueping Sun,Peng Wei,Gongchang Lu,Shixiong Sun,Yue Xu,Chun Fang,Qing Li,Jiantao Han
出处
期刊:Chemcatchem
[Wiley]
日期:2020-04-24
卷期号:12 (14): 3737-3745
被引量:31
标识
DOI:10.1002/cctc.202000494
摘要
Abstract Modulating intrinsic electronic and geometric structures of bimetallic electrocatalysts has been regarded as a promising strategy to effectively solve the sluggish kinetics and large overpotential of OER (Oxygen evolution reaction) and HER (Hydrogen evolution reaction) involved in future large‐scale electricity‐to‐hydrogen generation. Here, the bifunctional Co/Mo 2 C electrocatalysts encapsulated in 3D hierarchical nitrogen‐doped carbon nanofibers synchronously rooted with abundant carbon nanotubes (Co/Mo 2 C‐NCNTs) were successfully fabricated by a facile electrospinning method. Due to the unique heterostructures and strong synergetic effects between Co and Mo 2 C nanoparticles to improve OH − affinity, moderate Mo−H bonds, and expose more active sites, the Co/Mo 2 C‐NCNTs displayed a tiny overpotential for OER ( η 10 =310 mV) and HER ( η 10 =170 mV) and stably operated for 24 h. Moreover, the results of a water electrolysis device demonstrated that the faradaic efficiency was close to 100 %, which further proved that this method was feasible and effective to fabricate high‐efficiency bifunctional non‐noble electrocatalysts for water splitting.
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