| Literature DB >> 33558516 |
Zhi-Peng Wu1,2, Dominic T Caracciolo1, Yazan Maswadeh3, Jianguo Wen4, Zhijie Kong1, Shiyao Shan1, Jorge A Vargas3, Shan Yan1, Emma Hopkins1, Keonwoo Park1, Anju Sharma1, Yang Ren5, Valeri Petkov6, Lichang Wang7,8, Chuan-Jian Zhong9.
Abstract
Alloying noble metals with non-noble metals enables high activity while reducing the cost of electrocatalysts in fuel cells. However, under fuel cell operating conditions, state-of-the-art oxygen reduction reaction alloy catalysts either feature high atomic percentages of noble metals (>70%) with limited durability or show poor durability when lower percentages of noble metals (<50%) are used. Here, we demonstrate a highly-durable alloy catalyst derived by alloying PtPd (<50%) with 3d-transition metals (Cu, Ni or Co) in ternary compositions. The origin of the high durability is probed by in-situ/operando high-energy synchrotron X-ray diffraction coupled with pair distribution function analysis of atomic phase structures and strains, revealing an important role of realloying in the compressively-strained single-phase alloy state despite the occurrence of dealloying. The implication of the finding, a striking departure from previous perceptions of phase-segregated noble metal skin or complete dealloying of non-noble metals, is the fulfilling of the promise of alloy catalysts for mass commercialization of fuel cells.Entities:
Year: 2021 PMID: 33558516 DOI: 10.1038/s41467-021-21017-6
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919