Wang Chaohui, Zhang Jun, Miao Kanghua, Long Mairui, Lai Siyuan, Zhao Shijun, Kang Xiongwu
New Energy Research Institute, School of Environment and Energy, South China University of Technology, Guangzhou, 510006, China.
Department of Mechanical Engineering, City University of Hong Kong, Hong Kong, 999077, China.
Adv Mater. 2024 Aug;36(33):e2400433. doi: 10.1002/adma.202400433. Epub 2024 Jun 22.
Integrating high-entropy philosophy and nanocrystal-specific orientation into a single catalyst represents a promising strategy in development of high-performance catalysts. Nonetheless, shape-controlled synthesis of high-entropy alloy (HEA) nanocrystals is challenging owing to the distinct redox potentials and growth dynamics of metal elements. Herein, a one-pot co-reduction method is developed to fabricate ruthenium (Ru)-doped PtFeNiCuW octahedral HEA nanocrystals onto carbon nanotubes (Ru-PtFeNiCuW/CNTs). It is demonstrated that Ru dopants and W(CO) promote the concurrent reduction and growth of other metal precursors to obtain higher yield and larger size of HEA nanocrystals, despite low Ru content in Ru-PtFeNiCuW/CNTs. As an electrocatalyst toward hydrogen evolution reaction (HER), Ru-PtFeNiCuW/CNTs exhibits low overpotentials of 9, 16, and 34 mV at a current density of 10 mA cm and Tafel slopes of 19.2, 27.9, and 23.1 mV dec in acidic, alkaline, and neutral electrolytes, respectively. As a cathodic catalyst, Ru-PtFeNiCuW/CNTs operates for up to 1500 and 1200 h in acidic and alkaline electrolyte, respectively, at a current density of 50 mA cm in a two-electrode system for full water splitting. Theoretical calculations reveal accelerated kinetics of HO dissociation on W sites and *H desorption on hollow Cu-Cu-Cu and Cu-Cu-Pt sites.
将高熵理念与纳米晶体特定取向整合到单一催化剂中,是开发高性能催化剂的一种很有前景的策略。尽管如此,由于金属元素不同的氧化还原电位和生长动力学,高熵合金(HEA)纳米晶体的形状控制合成具有挑战性。在此,开发了一种一锅共还原法,以在碳纳米管(Ru-PtFeNiCuW/CNTs)上制备钌(Ru)掺杂的PtFeNiCuW八面体HEA纳米晶体。结果表明,尽管Ru-PtFeNiCuW/CNTs中的Ru含量较低,但Ru掺杂剂和W(CO)促进了其他金属前驱体的同时还原和生长,从而获得了更高产率和更大尺寸的HEA纳米晶体。作为析氢反应(HER)的电催化剂,Ru-PtFeNiCuW/CNTs在酸性、碱性和中性电解质中,在电流密度为10 mA cm时,过电位分别为9、16和34 mV,塔菲尔斜率分别为19.2、27.9和23.1 mV dec。作为阴极催化剂,在两电极全水解系统中,Ru-PtFeNiCuW/CNTs在酸性和碱性电解质中,在电流密度为50 mA cm时,分别可运行1500和1200 h。理论计算表明,HO在W位点上的解离动力学以及*H在空心Cu-Cu-Cu和Cu-Cu-Pt位点上的脱附动力学加快。