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氢氧化镍在阴离子交换膜水电解槽中促进硫化镍@氢氧化镍电催化活性和稳定性的三重作用。

Triple roles of Ni(OH) promoting the electrocatalytic activity and stability of NiS@Ni(OH) in anion exchange membrane water electrolyzers.

作者信息

Chai Hongmei, Ma Xu, Dang Yuechen, Zhang Yanqun, Yue Feng, Pang Xiangxiang, Wang Guangqing, Yang Chunming

机构信息

College of Chemistry & Chemical Engineering, Yan'an University, Yan'an Key Laboratory of Green Hydrogen Energy and Biomass Catalytic Conversion, Yan'an 716000, Shaanxi, China.

College of Chemistry & Chemical Engineering, Yan'an University, Yan'an Key Laboratory of Green Hydrogen Energy and Biomass Catalytic Conversion, Yan'an 716000, Shaanxi, China.

出版信息

J Colloid Interface Sci. 2024 Jan 15;654(Pt A):66-75. doi: 10.1016/j.jcis.2023.10.021. Epub 2023 Oct 7.

Abstract

Developing high performance and durable electrocatalysts is crucial for the practical application of large-scale water splitting under high current density. Here, we constructed a Mott-Schottky heterojunction bifunctional electrocatalyst coating of NiS with Ni(OH) thin film supported on Ni foam substrate (NiS@Ni(OH)) for anion exchange membrane water electrolyzers (AEMWEs). Remarkably, the η is as low as 274.6 mV toward the hydrogen evolution reaction and 423.8 mV toward the oxygen evolution reaction. AEMWEs deliver a stable performance that achieves current densities of 500 and 1000 mA cm at a cell voltage of 1.84 and 1.95 V, respectively. In particular, the NiS@Ni(OH) exhibits durable stability for 100 h at 500 mA cm without significant degradation and uses 0.75 kW·h of electricity less than commercial Ni foam electrode to produce each standard cubic meter of hydrogen gas at 500 mA cm. The excellent performance is ascribed to the triple roles of Ni(OH), which prevent the inner NiS from decomposing during the reaction process, promoting the dissociation of water and formation of adsorbed hydrogen intermediate and accelerating electron transfer ability due to the Mott-Schottky heterojunction between Ni(OH) and NiS. This work sheds light on the development of advanced bifunctional electrocatalysts based on non-precious transition metals for AEMWEs.

摘要

开发高性能且耐用的电催化剂对于在高电流密度下大规模水分解的实际应用至关重要。在此,我们构建了一种基于泡沫镍基底(NiS@Ni(OH))负载的Ni(OH)薄膜与NiS的Mott - Schottky异质结双功能电催化剂涂层,用于阴离子交换膜水电解槽(AEMWEs)。值得注意的是,析氢反应的过电位低至274.6 mV,析氧反应的过电位为423.8 mV。AEMWEs表现出稳定的性能,在电池电压为1.84 V和1.95 V时,分别实现了500和1000 mA cm²的电流密度。特别是,NiS@Ni(OH)在500 mA cm²的电流密度下表现出100 h的持久稳定性,且无明显降解,在500 mA cm²的电流密度下,每生产一标准立方米氢气比商用泡沫镍电极少用电0.75 kW·h。优异的性能归因于Ni(OH)的三重作用,即在反应过程中防止内部的NiS分解,促进水的离解和吸附氢中间体的形成,并由于Ni(OH)与NiS之间的Mott - Schottky异质结加速电子转移能力。这项工作为基于非贵金属过渡金属的AEMWEs先进双功能电催化剂的开发提供了思路。

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