RuNiOx前体对碱性整体水分解的定向拓扑常规调控

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2024-11-09 DOI:10.1002/cctc.202401664
Ziyan Cai, Minghao Yang, Xiaoke Xu, Xiuming Bu, Chuqian Xiao, Yikai Yang, Di Yin, Yuxuan Zhang, Wei Gao, Johnny C. Ho, Xianying Wang
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引用次数: 0

摘要

设计高效、稳定的析氢、析氧电催化剂是实现水分解系统绿色制氢的关键。双功能电催化剂的制备工艺简单,成本低,是一种很有前景的电催化剂。然而,单组分双功能催化剂往往难以匹配水的氧化还原电位,也难以同时对氢和氧中间体实现适当的吉布斯自由能吸附/解吸。本文通过精确控制RuNiOx前驱体的拓扑转变路径,成功制备了高性能的HER和OER用RuNi/Ni和Ru/NiO异质结构电催化剂。制备的电催化剂与水氧化还原电位之间的能级匹配证实了HER和OER的可行性。活性位点之间的协同作用确保了快速的中间吸附/解吸动力学。结果,组装的碱性整体水分解装置在2 V下实现了1 a cm−2的电流密度,并在100 mA cm−2下保持100小时的稳定运行。
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Targeted Topological Routine Regulation of RuNiOx Precursors for Excellent Alkaline Overall Water Splitting

Designing efficient and stable electrocatalysts for the hydrogen and oxygen evolution reactions (HER and OER) is crucial for green hydrogen production via the water-splitting system. The bifunctional electrocatalyst offers a promising strategy due to the simplified preparation process and reduced expenses. However, the single-component bifunctional catalysts often struggle to match the redox potential of water and to achieve proper adsorption/desorption of Gibbs free energy for both hydrogen and oxygen intermediates simultaneously. Herein, through precisely controlling the topological transformation path of the RuNiOx precursor, we successfully prepared high-performance RuNi/Ni and Ru/NiO heterostructure electrocatalysts for the HER and OER, respectively. The energy level matching between the fabricated electrocatalyst and water oxidation/reduction potential confirms the feasibility of HER and OER. The synergistic effect between the active sites ensures rapid intermediate adsorption/desorption kinetics. As a result, the assembled alkaline overall water splitting setup achieves a current density of 1 A cm−2 at 2 V and maintains stable operation at 100 mA cm−2 for 100 hours.

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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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