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用于高效碱性析氢的N修饰氧化镍表面

N-Modified NiO Surface for Superior Alkaline Hydrogen Evolution.

作者信息

Zhang Le, Liu Peng Fei, Li Yu Hang, Zu Meng Yang, Li Xu, Jiang Zheng, Wang Yun, Zhao Huijun, Yang Hua Gui

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, P.R. China.

Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201204, P.R. China.

出版信息

ChemSusChem. 2018 Mar 22;11(6):1020-1024. doi: 10.1002/cssc.201702371. Epub 2018 Feb 8.

Abstract

Boosting the sluggish kinetics of the hydrogen evolution reaction in alkaline environments is key for the large-scale application of water-alkali and chlor-alkali electrolysis. In this study, nitrogen atoms are used to precisely modulate electrochemical active sites on the surface of nickel oxide with low-coordinated oxygen atoms, to achieve enhanced kinetics in alkaline hydrogen evolution. Theoretical and experimental results demonstrate that surface charge redistribution after modulation facilitates both the initial water dissociation step and the subsequent recombination of H from low-coordinated oxygen sites and desorption of OH from nickel sites, thus accelerating the overall hydrogen evolution process. The N-modulated nickel oxide enriched in low-coordinated oxygen atoms exhibits significantly enhanced activity with a small overpotential of -100 mV at the current density of -10 mA cm and a robust stability over 90 h for hydrogen evolution in 1.0 m KOH.

摘要

提高碱性环境中析氢反应迟缓的动力学是水碱电解和氯碱电解大规模应用的关键。在本研究中,利用氮原子精确调控具有低配位氧原子的氧化镍表面的电化学活性位点,以实现碱性析氢动力学的增强。理论和实验结果表明,调制后的表面电荷重新分布有利于初始水离解步骤以及随后低配位氧位点的H重组和镍位点的OH脱附,从而加速了整体析氢过程。富含低配位氧原子的N调制氧化镍在电流密度为-10 mA cm时具有-100 mV的小过电位,表现出显著增强的活性,并且在1.0 m KOH中析氢90 h以上具有强大的稳定性。

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