氧还原反应
质子交换膜燃料电池
多孔性
氧气
碳纤维
化学工程
膜
质子
化学
燃料电池
材料科学
氧还原
还原(数学)
电化学
有机化学
物理化学
电极
复合材料
物理
量子力学
工程类
复合数
生物化学
数学
几何学
作者
Mengfei Qiao,Ying Wang,Quan Wang,Guangzhi Hu,Xamxikamar Mamat,Shusheng Zhang,Shuangyin Wang
标识
DOI:10.1002/ange.201914123
摘要
Abstract The low catalytic activity and poor mass transport capacity of platinum group metal free (PGM‐free) catalysts seriously restrict the application of proton‐exchange membrane fuel cells (PEMFCs). Catalysts derived from Fe‐doped ZIF‐8 could in theory be as active as Pt/C thanks to the high intrinsic activity of FeN 4 ; however, the micropores fail to meet rapid mass transfer. Herein, an ordered hierarchical porous structure is introduced into Fe‐doped ZIF‐8 single crystals, which were subsequently carbonized to obtain an FeN 4 ‐doped hierarchical ordered porous carbon (FeN 4 /HOPC) skeleton. The optimal catalyst FeN 4 /HOPC‐c‐1000 shows excellent performance with a half‐wave potential of 0.80 V in 0.5 m H 2 SO 4 solution, only 20 mV lower than that of commercial Pt/C (0.82 V). In a real PEMFC, FeN 4 /HOPC‐c‐1000 exhibits significantly enhanced current density and power density relative to FeN 4 /C, which does not have an optimized pore structure, implying an efficient utilization of the active sites and enhanced mass transfer to promote the oxygen reduction reaction (ORR).
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