沸石咪唑盐骨架
质子交换膜燃料电池
催化作用
材料科学
碳纤维
氧还原反应
燃料电池
化学工程
咪唑酯
氧还原
氧气
多金属氧酸盐
无机化学
金属有机骨架
电极
化学
电化学
有机化学
复合材料
复合数
物理化学
吸附
工程类
作者
Peng‐Yang Zhang,Xiaohua Yang,Qiaorong Jiang,Peixin Cui,Zhi‐You Zhou,Shuhui Sun,Yucheng Wang,Shi‐Gang Sun
标识
DOI:10.1021/acsami.2c04786
摘要
The oxygen reduction reaction (ORR) activity of the Fe/N/Carbon catalysts derived from the pyrolysis of zeolitic-imidazolate-framework-8 (ZIF-8) has been still lower than that of commercial Pt-based catalysts utilized in the proton exchange membrane fuel cells (PEMFCs) due to low density of accessible active sites. In this study, an efficient carbon-supporting strategy is developed to enhance the ORR efficiency of the ZIF-derived Fe/N/Carbon catalysts by increasing the accessible active site density. The enhancement lies in (i) improving the accessibility of active sites via converting dodecahedral particles to graphene-like layered materials and (ii) enhancing the density of FeNx active sites via suppressing the formation of nanoparticles as well as providing extra spaces to host active sites. The optimized and efficient Fe/N/Carbon catalyst shows a half-wave potential (E1/2) of 0.834 V versus reversible hydrogen electrode in acidic media and produces a peak power density of 0.66 W cm–2 in an air-fed PEMFC at 2 bar backpressure, outperforming most previously reported Pt-free ORR catalysts. Finally, the general applicability of the carbon-supporting strategy is confirmed using five different commercial carbon blacks. This work provides an effective route to derive Fe/N/Carbon catalysts exhibiting a higher power density in PEMFCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI