过电位
电催化剂
非阻塞I/O
催化作用
电解水
镍
电解
无机化学
化学
贵金属
氧化物
电解质
金属
过渡金属
析氧
化学工程
分解水
材料科学
电化学
物理化学
电极
有机化学
光催化
工程类
作者
Chi‐Huang Chuang,Pei‐Hao Kang,Yung‐Yu Lai,Cheng‐Hung Hou,Wei‐Che Tseng,Yan‐Jia Huang,Mu‐Huai Fang,Jing‐Jong Shyue,Chao‐Cheng Kaun,Yuh‐Jen Cheng
出处
期刊:Chemsuschem
[Wiley]
日期:2023-07-08
卷期号:16 (17): e202300820-e202300820
被引量:6
标识
DOI:10.1002/cssc.202300820
摘要
Abstract High activity catalysts for hydrogen evolution reaction (HER) play a key role in converting renewable electricity to storable hydrogen fuel. Great effort has been devoted to the search for noble metal free catalysts to make electrolysis viable for practical applications. Here, a non‐precious metal oxide/metal catalyst with high intrinsic activity comparable to Pt/C was reported. The electrocatalyst consisting of NiO, Ni(OH) 2 , Cr 2 O 3 , and Ni metal exhibits a low overpotential of 27, 103, and 153 mV at current densities of 10, 100, and 200 mA cm −2 , respectively, in a 1.0 m NaOH electrolyte. The activity is much higher than that of NiO x /Ni or Cr 2 O 3 alone, showing the synergistic effect of NiO x /Ni and Cr 2 O 3 on catalyzing HER. Density functional theory calculations shows that NiO and Cr 2 O 3 on Ni surface lower the disassociation energy barrier for breaking H−OH bond, while Ni(OH) 2 and Cr 2 O 3 create preferred sites on Ni surface with near‐zero H* adsorption free energy to promote H* to gaseous H 2 evolution. These synergistic effects of multiple‐oxides/metal composition enhance the disassociation of H−OH and the evolution of H* to gaseous H 2 , thus achieving high activity and demonstrating a promising composition design for noble metal free catalyst.
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