Li Jie, Wang Xue, Yu Jun, Xu Kai, Jia Zhe, Li Hongkun, Ren Lei, Yang Yiyuan, Chang Keke, Li Yangyang, Liu Xiangfa, Lu Jian, Liu Sida
Key Laboratory for Liquid-Solid Structural Evolution & Processing of Materials, Ministry of Education, Shandong University, Jinan, 250061, China.
Key Laboratory of Advanced Marine Materials, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang, 315201, China.
Adv Sci (Weinh). 2025 Jul;12(27):e2501976. doi: 10.1002/advs.202501976. Epub 2025 Apr 26.
Development of active and cost-effective electrocatalysts to substitute platinum-based catalysts in alkaline hydrogen evolution reactions (HERs) remains a challenge. The synergistic effect between different elements in alloy catalysts can regulate electronic structure and thereby provide an abundance of catalytic sites for reactions. Thus, alloy catalysts are suitable candidates for future energy applications. Conventional methods for enhancing the performance of alloy catalysts have mainly focused on element composition and thus have often neglected to examine catalyst design. In this paper, a ruthenium-manganese-niobium alloy catalyst (RuMn12NbO) is reported with a supra-nanocrystalline dual-phase structure that is fabricated through combinatorial magnetron co-sputtering at ambient temperatures. The induced crystal-crystal heterostructure of RuMnNbO reduced system energy, thereby achieving balance between stability and catalytic activity. RuMnNbO exhibited excellent HER performance, as demonstrated by low HER overpotential (18 mV at 10 mA cm) and robust stability (300 h at 1.2 A cm). Moreover, oxygen-rich interfaces in RuMnNbO enhanced charge transfer and the kinetics of water dissociation as well as optimized hydrogen adsorption/desorption processes, thus boosting HER performance. The crystal-crystal heterostructure and oxygen-rich interfaces in RuMnNbO are induced by its dual-phase nanocrystalline structure, which represents a new structural design for enhancing the performance of catalysts for sustainable energy development.
开发活性高且经济高效的电催化剂以替代碱性析氢反应(HER)中的铂基催化剂仍然是一项挑战。合金催化剂中不同元素之间的协同效应可以调节电子结构,从而为反应提供大量催化位点。因此,合金催化剂是未来能源应用的合适候选材料。传统的提高合金催化剂性能的方法主要集中在元素组成上,因此常常忽略了对催化剂设计的研究。本文报道了一种具有超纳米晶双相结构的钌 - 锰 - 铌合金催化剂(RuMn12NbO),它是通过在室温下组合磁控共溅射制备的。RuMnNbO诱导的晶 - 晶异质结构降低了系统能量,从而在稳定性和催化活性之间实现了平衡。RuMnNbO表现出优异的HER性能,低HER过电位(在10 mA cm时为18 mV)和强大的稳定性(在1.2 A cm下300小时)证明了这一点。此外,RuMnNbO中富含氧的界面增强了电荷转移和水离解动力学以及优化了氢吸附/解吸过程,从而提高了HER性能。RuMnNbO中的晶 - 晶异质结构和富含氧的界面是由其双相纳米晶结构诱导产生的,这代表了一种用于提高可持续能源发展催化剂性能的新结构设计。