Zeng Biao, Liu Xinzheng, Wan Li, Xia Chenghui, Cao Lixin, Hu Yubin, Dong Bohua
School of Materials Science and Engineering, Ocean University of China, 1299 Sansha Road, Qingdao, Shandong Province, 266400, P. R. China.
Institute of Marine Science and Technology, Shandong University, 72 Coastal Highway, Qingdao, 266237, P. R. China.
Angew Chem Int Ed Engl. 2024 Apr 8;63(15):e202400582. doi: 10.1002/anie.202400582. Epub 2024 Feb 20.
Large-scale deployment of proton exchange membranes water electrolysis (PEM-WE) requires a substantial reduction in usage of platinum group metals (PGMs) as indispensable electrocatalyst for cathodic hydrogen evolution reaction (HER). Ultra-fine PGMs nanocatalysts possess abundant catalytic sites at lower loading, but usually exhibit reduced stability in long-term operations under corrosive acidic environments. Here we report grafting the ultra-fine PtRu crystalline nanoalloys with PtRuSe "amorphous skin" (c-PtRu@a-PtRuSe) by in situ atomic layer selenation to simultaneously improve catalytic activity and stability. We found that the c-PtRu@a-PtRuSe-1 with ~0.6 nm thickness amorphous skin achieved an ultra-high mass activity of 26.7 A mg at -0.07 V as well as a state-of-the-art durability maintained for at least 1000 h at -10 mA cm and 550 h at -100 mA⋅cm for acid HER. Experimental and theoretical investigations suggested that the amorphous skin not only improved the electrochemical accessibility of the catalyst surface and increasing the intrinsic activity of the catalytic sites, but also mitigated the dissolution/diffusion of the active species, thus resulting in improved catalytic activity and stability under acidic electrolyte. This work demonstrates a direction of designing ultra-fine PGMs electrocatalysts both with high utilization and robust durability, offers an in situ "amorphous skin" engineering strategy.
质子交换膜水电解(PEM-WE)的大规模部署需要大幅减少铂族金属(PGM)的用量,因为PGM是阴极析氢反应(HER)不可或缺的电催化剂。超细PGM纳米催化剂在较低负载量下具有丰富的催化位点,但在腐蚀性酸性环境中的长期运行中通常表现出稳定性下降。在此,我们报告通过原位原子层硒化将超细PtRu晶体纳米合金与PtRuSe“非晶态表皮”(c-PtRu@a-PtRuSe)接枝,以同时提高催化活性和稳定性。我们发现,具有约0.6纳米厚非晶态表皮的c-PtRu@a-PtRuSe-1在-0.07伏时实现了26.7安/毫克的超高质量活性,以及在-10毫安/平方厘米下至少保持1000小时和在-100毫安/平方厘米下保持550小时的最先进耐久性,用于酸性HER。实验和理论研究表明,非晶态表皮不仅提高了催化剂表面的电化学可及性并增加了催化位点的本征活性,还减轻了活性物种的溶解/扩散,从而在酸性电解质下提高了催化活性和稳定性。这项工作展示了设计具有高利用率和强大耐久性的超细PGM电催化剂的方向,提供了一种原位“非晶态表皮”工程策略。