催化作用
电催化剂
杂原子
化学
碳纤维
化学工程
氧气
电解质
吸附
电化学
无机化学
氟化铵
微生物燃料电池
材料科学
有机化学
电极
阳极
工程类
物理化学
复合材料
复合数
戒指(化学)
作者
Kengqiang Zhong,Henghui You,Lei Huang,Han Li,Linzhe Huang,Xianjie Liu,Hongguo Zhang
标识
DOI:10.1016/j.jpowsour.2023.233232
摘要
The metal-free carbon-based catalyst with low cost and high oxygen reduction reaction (ORR) activity is urgently desired to satisfy the demands of microbial fuel cells (MFCs). However, it is still a great challenge to develop a facile and feasible strategy to construct efficient active sites of heteroatom doping for carbon-based electrocatalyst. Herein, we report a strategy based on an ammonium fluoride (NH4F) gas-steamed metal-organic frameworks (MOFs) to heighten structural defects and density of N, F active sites of metal-free catalyst. Oxygen temperature-programmed deposition and density functional theory results confirm that the NH4F gas-steamed process greatly enhances the adsorption affinity of O2 and oxygen intermediates on the catalysts. The resulted N and F co-doped porous carbon cage (FNC-15) demonstrates outstanding ORR catalytic activity and long-term stability in alkaline and neutral electrolytes. This work proposes a facile and efficient in situ gas-steamed strategy to develop metal-free cathode catalysts with superior performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI