Li Yakang, Guo Jiaxin, Wang Ruguang, Zhao Yang, Wang Quanlu, Li Jisi, Ling Tao
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.
ACS Appl Mater Interfaces. 2025 Feb 5;17(5):7784-7792. doi: 10.1021/acsami.4c19204. Epub 2025 Jan 27.
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.
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。