催化作用
氧还原反应
氧气
质子交换膜燃料电池
化学
氧还原
燃料电池
氧原子
质子
膜
光化学
无机化学
Atom(片上系统)
化学工程
电化学
物理化学
有机化学
分子
电极
生物化学
物理
量子力学
计算机科学
工程类
嵌入式系统
作者
Junming Luo,Yating Zhang,Zhe Lü,Chao Liu,Yueshan Xu,Hui Chen,Qi Wang,Daoxiong Wu,Dai Dang,Yijie Deng,Peng Rao,Peilin Deng,Jing Li,Zhengpei Miao,Xinlong Tian
标识
DOI:10.1002/ange.202500500
摘要
Carbon‐supported metal single‐atom catalysts (M‐SACs) are promising oxygen reduction reaction (ORR) catalysts. Their ORR activity and selectivity are significantly affected by the heteroatoms that coordinate the central metal atoms. Previous reports found that oxygen‐coordinated M‐SACs promoted a 2e‐ ORR rather than the 4e‐ ORR that is more desirable for fuel cells. Herein, we report for the first time that oxygen‐coordinated M‐SACs are capable of promoting the 4e‐ ORR in acid media. We prepared a Cr(acac)‐NC catalyst with the central Cr atom coordinated by two O atoms. The Cr(acac)‐NC catalyst not only exhibits excellent ORR activity and stability in acid media, but also delivers high proton exchange membrane fuel cell (PEMFC) performance comparable to N‐coordinated M‐SACs. Density functional theory (DFT) calculations reveal that Cr‐O2 moieties located on the zigzag edge of the carbon support are the ORR‐active sites.
科研通智能强力驱动
Strongly Powered by AbleSci AI