双金属片
双功能
电催化剂
石墨烯
氧化物
材料科学
纳米颗粒
电解
分解水
析氧
可逆氢电极
碱性水电解
化学工程
纳米技术
无机化学
催化作用
化学
冶金
电解质
电化学
金属
电极
工作电极
物理化学
工程类
光催化
生物化学
作者
Dong‐Eun Lee,Satyanarayana Moru,Kasala Prabhakar Reddy,Wan-Kuen Jo,Surendar Tonda
标识
DOI:10.1016/j.apsusc.2023.156928
摘要
Water electrolysis is regarded as the most promising method for developing sustainable energy technologies. However, low-cost bifunctional electrocatalysts with high efficacy and long-term stability are required to make this method economically viable. Core-shell nanoparticles, which comprise a thin layer of a catalytically active shell surrounding a subsurface core, have recently emerged as cutting-edge electrocatalysts for effective water electrolysis. Herein, we systematically fabricated distinct bimetallic Cu–Ni particles by tuning the Cu:Ni ratios, and then anchored them to an N-doped reduced graphene oxide (NRG) backbone for alkaline water splitting. A Cu:Ni molar ratio of 1:1 was determined to be optimal for forming an effective core–shell configuration, affording favorable adsorption energies toward reactants. The Cu–Ni(1:1) core–shell nanoparticles anchored NRG, termed Cu–Ni(1:1)@NRG, displayed excellent performance toward the H2 evolution reaction (HER) and oxygen evolution reaction (OER), with overpotentials at 10 mA cm−2 of 107 and 310 mV, respectively, versus a reversible hydrogen electrode (RHE). This current density (10 mA cm−2) was attained at a low cell voltage of 1.64 V when Cu–Ni(1:1)@NRG was used as the bifunctional electrocatalyst for alkaline water electrolysis. Furthermore, the Cu–Ni(1:1)@NRG electrocatalyst exhibited outstanding long-term stability in prolonged electrocatalytic studies at a constant current density.
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