电催化剂
材料科学
双金属片
催化作用
分解水
析氧
化学工程
钴
可逆氢电极
电化学
石墨烯
合金
无机化学
纳米技术
化学
金属
电极
工作电极
复合材料
物理化学
冶金
有机化学
光催化
工程类
作者
Riyue Ge,Juanjuan Huo,Ying Li,Ting Liao,Jiujun Zhang,Mingyuan Zhu,Tansir Ahamad,Sean Li,Hao Liu,Lingyan Feng,W. X. Li
摘要
The rational construction of highly efficient electrocatalysts comprising multiple components with distinctive bifunctionalities is still a challenge for the practical application due to their sluggish kinetics for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Here, a series of cobalt-molybdenum alloy nanorods encapsulated in N-doped carbon shells (CoMo@NC) is synthesized via an in-situ carbonization-reduction method using CoMoO4 as precursor. The high conductivity, strain-induced effect, and synergistic interactions between N-doped carbon and bimetallic cores endow the optimized catalyst with outperforming catalytic performances for HER and OER in alkaline solution with low overpotentials (98 mV for HER and 336 mV for OER at 10 mA cm-2), as well as high durability. The overall water splitting device using CoMo@NC-800 as bi-functional catalyst could possess a low voltage of 1.67 V to drive a current density of 10 mA cm-2 and high durability. Furthermore, density functional theory calculations reveal that the pyridinic-N atoms of graphene anchored on CoMo alloy nanoparticles can efficiently modulate the electronic structure to generate an optimal free energy of hydrogen adsorption (-0.029 eV), suggesting excellent HER intrinsic activity. This work may provide a facile avenue to achieve a multiple metallic alloy-based nanomaterial for boosting electrochemical water splitting performance.in
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