催化作用
碳纤维
选择性
热解
酞菁
化学工程
色散(光学)
材料科学
金属有机骨架
化学
铂金
无机化学
有机化学
电化学
物理化学
电极
吸附
物理
复合材料
复合数
工程类
光学
作者
Zhengping Zhang,Junting Sun,Feng Wang,Liming Dai
标识
DOI:10.1002/ange.201804958
摘要
Abstract Single Fe atoms dispersed on hierarchically structured porous carbon (SA‐Fe‐HPC) frameworks are prepared by pyrolysis of unsubstituted phthalocyanine/iron phthalocyanine complexes confined within micropores of the porous carbon support. The single‐atom Fe catalysts have a well‐defined atomic dispersion of Fe atoms coordinated by N ligands on the 3D hierarchically porous carbon support. These SA‐Fe‐HPC catalysts are comparable to the commercial Pt/C electrode even in acidic electrolytes for oxygen reduction reaction (ORR) in terms of the ORR activity ( E 1/2 =0.81 V), but have better long‐term electrochemical stability (7 mV negative shift after 3000 potential cycles) and fuel selectivity. In alkaline media, the SA‐Fe‐HPC catalysts outperform the commercial Pt/C electrode in ORR activity ( E 1/2 =0.89 V), fuel selectivity, and long‐term stability (1 mV negative shift after 3000 potential cycles). Thus, these nSA‐Fe‐HPCs are promising non‐platinum‐group metal ORR catalysts for fuel‐cell technologies.
科研通智能强力驱动
Strongly Powered by AbleSci AI