非阻塞I/O
过电位
化学
催化作用
微晶
吸附
化学工程
氢
镍
无机化学
电化学
物理化学
电极
有机化学
结晶学
工程类
作者
Kailu Guo,Xiaoyan Lu,Jinzhi Jia,Zhan Zhou,Junfeng Huang,Shuang Wang,Shi-Hui Li,Haixia Wu,Cailing Xu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-05-31
卷期号:62 (23): 9249-9258
被引量:5
标识
DOI:10.1021/acs.inorgchem.3c01212
摘要
Precatalyst reconstruction in alkaline hydrogen evolution reaction (HER) usually leads to changes in the morphology, composition, and structure, thus improving the catalytic activity, which recently receives intensive attention. However, the design strategies of cathodic reconstruction and the structural features of reconstruction products have not achieved a profound understanding. Here, from the point of thermodynamic stability, metastable nickel selenite dihydrate (NiSeO3·2H2O) is deliberately fabricated as a precatalyst to comprehensively study the reconstruction dynamics in alkaline HER. Multiple in/ex situ techniques capture the geometric, component, and phase evolutions, proving that NiSeO3·2H2O can be transformed into SeO32--decorated polycrystalline NiO nanosheets with rich active sites and good conductivity under alkaline HER conditions, which act as a real catalytic active species. Density functional theory calculations demonstrate that the adsorption of SeO32- can further promote the HER activity of NiO due to the optimized free energy of water activation and hydrogen adsorption. As a result, the SeO32--NiO catalyst exhibits a low overpotential at -10 mA cm-2 (90 mV) and long-term stability (>100 h). This work highlights the targeted design of precatalyst to trigger and utilize cathodic reconstruction and provides an available method for the development of adsorption-modulated efficient electrocatalysts.
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