Fe Single-Atom Catalysts on MOF-5 Derived Carbon for Efficient Oxygen Reduction Reaction in Proton Exchange Membrane Fuel Cells

被引:236
作者
Xie, Xiaoying [1 ]
Shang, Lu [1 ]
Xiong, Xuyang [1 ]
Shi, Run [1 ]
Zhang, Tierui [1 ,2 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Fe single-atom catalysts; MOF-5; oxygen reduction reaction; PEMFCs; porous carbon; N-DOPED CARBON; METAL-ORGANIC FRAMEWORK; POROUS CARBON; ACTIVE-SITES; C ELECTROCATALYST; ORR CATALYST; IRON ATOMS; NITROGEN; NANOTUBES; FE/N/C;
D O I
10.1002/aenm.202102688
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of Fe single-atom catalysts (Fe SACs) with abundant, accessible Fe sites is a key step toward enhancing the efficiency of the oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs). In this study, Zn4O(1,4-benzenedicarboxylate)(3) (MOF-5), which has a 3D microporous cubic structure, is used as the precursor to prepare highly-porous carbon (denoted as C-MOF-5) with an ultrahigh specific surface area (2751 m(2) g(-1)) and high external surface area (1651 m(2) g(-1)). C-MOF-5 is demonstrated as an effective carbon support to yield Fe SAC-MOF-5 with a large amount of accessible FeNx sites (2.35 wt%). Fe SAC-MOF-5 delivers a half-wave potential of 0.83 V (vs RHE) in a 0.5 m H2SO4 electrolyte, and achieves a peak power density of 0.84 W cm(-2) in a 0.2 MPa H-2-O-2 PEMFC. This excellent performance originates from the ultrahigh specific surface area of C-MOF-5 for the formation of a high density of single Fe atoms, and high external surface area for the increased exposure of active sites. This work may inspire the rational design of metal single-atom catalysts derived from a wider range of MOF precursors with ultrahigh specific area to improve the performance of the oxygen reduction reaction in PEMFCs.
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页数:8
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