Highly active and durable core–shell electrocatalysts for proton exchange membrane fuel cells
Hsiwen Wu, Fei Xiao, Jing Wang, Meng Gu, Minhua Shao
Abstract
This work presents simple post-treatment methods to selectively and partially remove the Pd core of Pd–Pt core–shell (Pt@Pd/C) catalysts. The proton exchange membrane fuel cell with the post-treated Pt@Pd/C cathode (Pt loading: 0.10 mg·cm−2) delivers an impressive peak power density of 1.2 W·cm−2. The partial removal of Pd core endows an ultrahigh oxygen reduction reaction (ORR) mass activity of 0.32 A·mgPGM−1 when normalized to the platinum group metal (PGM) mass, or equivalently 0.55 A·mgPt−1 at 0.9 V measured in a fuel cell. The post-treatment thickens the Pt shells and mitigates the Pd dissolution during potential cycling. As a result, the post-treated core–shell catalyst demonstrates superior durability in ORR mass activity and polarization power density retention than untreated core–shell catalyst and benchmark Pt/C. In-situ inductively coupled plasma-mass spectrometry (ICP-MS) results highlight that the amount of dissolved Pd in post-treated core–shell catalyst is 17-times lower than that of the untreated one. Our findings highlight the importance of structural tuning of catalysts in enhancing their mass activity and durability.