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Hierarchically Ordered Porous Carbon with Atomically Dispersed FeN 4 for Ultraefficient Oxygen Reduction Reaction in Proton‐Exchange Membrane Fuel Cells
Author(s) -
Qiao Mengfei,
Wang Ying,
Wang Quan,
Hu Guangzhi,
Mamat Xamxikamar,
Zhang Shusheng,
Wang Shuangyin
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201914123
Subject(s) - proton exchange membrane fuel cell , catalysis , carbonization , materials science , carbon fibers , mass transfer , chemical engineering , porosity , membrane , oxygen reduction reaction , oxygen , metal organic framework , chemistry , electrochemistry , electrode , organic chemistry , composite material , adsorption , chromatography , biochemistry , composite number , engineering , scanning electron microscope
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).