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用于加速碱性析氢反应的表面含金属钌的氧化钌电催化剂的设计

Design of RuO Electrocatalysts Containing Metallic Ru on the Surface to Accelerate the Alkaline Hydrogen Evolution Reaction.

作者信息

Li Yakang, Guo Jiaxin, Wang Ruguang, Zhao Yang, Wang Quanlu, Li Jisi, Ling Tao

机构信息

Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Institute of New-Energy, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.

出版信息

ACS Appl Mater Interfaces. 2025 Feb 5;17(5):7784-7792. doi: 10.1021/acsami.4c19204. Epub 2025 Jan 27.

Abstract

The development of water splitting technology in alkaline medium requires the exploration of electrocatalysts superior to Pt/C to boost the alkaline hydrogen evolution reaction (HER). Ruthenium oxides with strong water dissociation ability are promising candidates; however, the lack of hydrogen combination sites immensely limits their performance. Herein, we reported a unique RuO catalyst with metallic Ru on its surface through a simple cation exchange method. We demonstrated that the formation of metallic Ru on RuO greatly enhances the interaction between the catalyst and adsorbed hydrogen (*H), resulting in extremely high HER activity in alkaline media. Moreover, we proposed the potential of zero charge () as a descriptor of ruthenium-base catalysts for alkaline HER for the first time and revealed that the existence of metallic Ru optimizes the of RuO toward the hydrogen region. As a result, the designed RuO catalyst achieves an overpotential of only 18 mV at the current density of 10 mA cm. Furthermore, RuO requires 1.80 V to reach 800 mA cm in the anion exchange membrane water electrolyzer, outperforming the benchmark Pt/C.

摘要

碱性介质中析氢技术的发展需要探索比Pt/C更优异的电催化剂来促进碱性析氢反应(HER)。具有强水解离能力的氧化钌是很有潜力的候选材料;然而,缺乏氢结合位点极大地限制了它们的性能。在此,我们通过一种简单的阳离子交换方法报道了一种表面带有金属Ru的独特RuO催化剂。我们证明了RuO表面金属Ru的形成极大地增强了催化剂与吸附氢(*H)之间的相互作用,从而在碱性介质中产生了极高的HER活性。此外,我们首次提出零电荷电位()作为钌基催化剂碱性HER描述符的潜力,并揭示了金属Ru的存在使RuO的零电荷电位向氢区域优化。结果,所设计的RuO催化剂在电流密度为10 mA cm时的过电位仅为18 mV。此外,在阴离子交换膜水电解槽中,RuO达到800 mA cm需要1.80 V,性能优于基准Pt/C。

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