电催化剂
材料科学
催化作用
质子交换膜燃料电池
溶解
化学工程
电解质
氧还原反应
纳米颗粒
原电池
纳米结构
氧还原
单排替反应
镍
铂金
纳米技术
电化学
无机化学
电极
物理化学
冶金
化学
有机化学
工程类
作者
Xiao Lyu,Yi Jia,Xin Mao,Daohao Li,Gen Li,Linzhou Zhuang,Xin Wang,Dongjiang Yang,Qiang Wang,Aijun Du,Xiangdong Yao
标识
DOI:10.1002/adma.202003493
摘要
Manipulating the surface structure of electrocatalysts at the atomic level is of primary importance to simultaneously achieve the activity and stability dual-criteria in oxygen reduction reaction (ORR) for proton exchange membrane fuel cells. Here, a durable acidic ORR electrocatalyst with the "defective-armored" structure of Pt shell and Pt-Ni core nanoparticle decorated on graphene (Pt-Ni@PtD /G) using a facile and controllable galvanic replacement reaction to generate gradient distribution of Pt-Ni composition from surface to interior, followed by a partial dealloying approach, leaching the minor nickel atoms on the surface to generate defective Pt skeleton shell, is reported. The Pt-Ni@PtD /G catalyst shows impressive performance for ORR in acidic (0.1 m HClO4 ) electrolyte, with a high mass activity of threefold higher than that of Pt/C catalyst owing to the tuned electronic structure of locally concave Pt surface sites through synergetic contributions of Pt-Ni core and defective Pt shell. More importantly, the electrochemically active surface areas still retain 96% after 20 000 potential cycles, attributing to the Pt atomic shell acting as the protective "armor" to prevent interior Ni atoms from further dissolution during the long-term operation.
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