提高镍基电极分水制氢能力的电解质添加剂策略

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Pengbo Xiang, Yanqi Li, Jie Zheng, Bingbing Sun, Chi Zhang, Zhangyi Tao, Weijie Xia, Ming Ge, Xiaolei Yuan and Zhao Cai*, 
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引用次数: 0

摘要

可持续水电解已成为生产绿色氢的未来技术。改善水裂解制氢的一般方法是开发新型电极材料。在这项工作中,我们报道了一种正交方法,即调节电解质成分。为了验证这一概念,在电解液中加入了Na2S添加剂,以提高ni基电极的水分解性能。采用微量Na2S (50 mM)作为电解液添加剂,使Ni(OH)2电极在10 mA cm-2下析氢过电位从262 mV降至193 mV。原位拉曼研究揭示了电催化过程中NiS活性相和S-H键的形成,这是性能提高的原因。此外,这种电解质添加剂策略在其他镍基材料(如金属镍泡沫)、其他电解质(如盐水)和其他催化反应体系(如析氧)中也取得了成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Electrolyte Additive Strategy for Enhancing Water-Splitting Hydrogen Production of Nickel-Based Electrodes

An Electrolyte Additive Strategy for Enhancing Water-Splitting Hydrogen Production of Nickel-Based Electrodes

Sustainable water electrolysis has emerged as a future technology for producing green hydrogen. The general approach to improving water-splitting hydrogen production is to develop novel electrode materials. In this work, we reported an orthogonal approach, namely, regulating the electrolyte components. As a proof of concept, Na2S additive was introduced to the electrolytes to enhance the water-splitting performance of Ni-based electrodes. Specifically, a tiny amount of Na2S (50 mM) was employed as an electrolyte additive to reduce the hydrogen evolution overpotential of the Ni(OH)2 electrode from 262 to 193 mV at 10 mA cm–2. In situ Raman studies unveiled the formation of the NiS active phase and the S–H bond during electrocatalysis, which were responsible for such a performance improvement. Moreover, such an electrolyte additive strategy also showed its success in other Ni-based materials such as metallic Ni foam, other electrolytes such as saline water, and other catalytic reaction systems such as oxygen evolution.

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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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