Zhang Tao, Liu Qingyi, Bao Haoming, Wang Mingyue, Wang Nana, Zhang Bao, Fan Hong Jin
School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, 637371, Singapore.
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore, 637371, Singapore.
Nat Commun. 2025 Jan 25;16(1):1037. doi: 10.1038/s41467-025-56189-y.
Designing efficient Ruthenium-based catalysts as practical anodes is of critical importance in proton exchange membrane water electrolysis. Here, we develop a self-assembly technique to synthesize 1 nm-thick rutile-structured high-entropy oxides (RuIrFeCoCrO) from naked metal ions assembly and oxidation at air-molten salt interface. The RuIrFeCoCrO requires an overpotential of 185 mV at 10 m A cm and maintains the high activity for over 1000 h in an acidic electrolyte via the adsorption evolution mechanism. We discuss the role of each element in the RuIrFeCoCrO and find that the Cr, Co, and Ir sites contribute to the catalytic activity, while the Cr atoms weaken the Ru-O bond covalency and improves the catalyst stability. The assembled proton exchange membrane electrolyzer operates stably for more than 600 h at a large current of 1 A cm. The naked ion assembly demonstrated in this work may provide an effective pathway for the controlled synthesis of a diversity of high-entropy materials.
设计高效的钌基催化剂作为实用阳极在质子交换膜水电解中至关重要。在此,我们开发了一种自组装技术,通过在空气 - 熔盐界面处裸金属离子的组装和氧化来合成1纳米厚的金红石结构高熵氧化物(RuIrFeCoCrO)。RuIrFeCoCrO在10 mA cm时需要185 mV的过电位,并通过吸附析氧机制在酸性电解质中保持超过1000小时的高活性。我们讨论了RuIrFeCoCrO中各元素的作用,发现Cr、Co和Ir位点有助于催化活性,而Cr原子削弱了Ru - O键的共价性并提高了催化剂稳定性。组装的质子交换膜电解槽在1 A cm的大电流下稳定运行超过600小时。这项工作中展示的裸离子组装可能为多种高熵材料的可控合成提供有效途径。