双金属片
钴
铂金
催化作用
材料科学
纳米结构
电催化剂
退火(玻璃)
浸出(土壤学)
纳米技术
化学工程
无机化学
电化学
化学
冶金
电极
金属
物理化学
工程类
土壤科学
土壤水分
生物化学
环境科学
作者
Lei Wang,Wenpei Gao,Zhenyu Liu,Zhenhua Zeng,Yifan Liu,Michael Giroux,Miaofang Chi,Guofeng Wang,Jeffrey Greeley,Xiaoqing Pan,Chao Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-11-09
卷期号:8 (1): 35-42
被引量:82
标识
DOI:10.1021/acscatal.7b02501
摘要
Pt-bimetallic alloys involving 3d transition metals (Co, Ni, etc.) are promising electrocatalysts for the oxygen reduction reaction (ORR). Despite the enhanced catalytic activity versus Pt, the electrocatalytic performance of Pt-bimetallic catalysts is however limited by the lack of long-term durability, primarily due to the leaching of the non-noble element under harsh electrochemical conditions. Our study shows that the core–shell nanostructure comprising a Pt shell and a cobalt core (denoted as Co@Pt) could overcome this limitation, demonstrating ∼10 times improvement in catalytic activity versus commercial Pt catalysts and no more than 13% of loss after 30000 potential cycles. The evolutions of nanoscale and surface structures over the course of extensive potential cycling were followed by combining electron microscopic elemental mapping and electrochemical studies of CO stripping. Atomistic simulations and density functional theory calculations suggest that the core–shell nanostructure could protect the non-noble cobalt from leaching under the "electrochemical annealing" conditions while maintaining the beneficial mechanisms of bimetallic systems for catalytic activity enhancement.
科研通智能强力驱动
Strongly Powered by AbleSci AI