| Literature DB >> 31769154 |
Mengfei Qiao1,2, Ying Wang1,2, Quan Wang1, Guangzhi Hu1,3, Xamxikamar Mamat2, Shusheng Zhang3, Shuangyin Wang4.
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 FeN4 ; 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 FeN4 -doped hierarchical ordered porous carbon (FeN4 /HOPC) skeleton. The optimal catalyst FeN4 /HOPC-c-1000 shows excellent performance with a half-wave potential of 0.80 V in 0.5 m H2 SO4 solution, only 20 mV lower than that of commercial Pt/C (0.82 V). In a real PEMFC, FeN4 /HOPC-c-1000 exhibits significantly enhanced current density and power density relative to FeN4 /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).Entities:
Keywords: fuel cells; mass transfer; mesoporous materials; oxygen reduction reaction; zeolite analogues
Year: 2020 PMID: 31769154 DOI: 10.1002/anie.201914123
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336