TY - JOUR
T1 - Self-Templated Hierarchically Porous Carbon Nanorods Embedded with Atomic Fe-N4 Active Sites as Efficient Oxygen Reduction Electrocatalysts in Zn-Air Batteries
AU - Gong, Xiaofei
AU - Zhu, Jianbing
AU - Li, Jiazhan
AU - Gao, Rui
AU - Zhou, Qingyan
AU - Zhang, Zhen
AU - Dou, Haozhen
AU - Zhao, Lei
AU - Sui, Xulei
AU - Cai, Jiajun
AU - Zhang, Yunlong
AU - Liu, Bing
AU - Hu, Yongfeng
AU - Yu, Aiping
AU - Sun, Shu hui
AU - Wang, Zhenbo
AU - Chen, Zhongwei
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2021/2/17
Y1 - 2021/2/17
N2 - Iron-nitrogen-carbon materials are being intensively studied as the most promising substitutes for Pt-based electrocatalysts for the oxygen reduction reaction (ORR). A rational design of the morphology and porous structure can promote the accessibility of the active site and the reactants/products transportation, accelerating the reaction kinetics. Herein, 1D porous iron/nitrogen-doped carbon nanorods (Fe/N-CNRs) with a hierarchically micro/mesoporous structure are prepared by pyrolyzing the in situ polymerized pyrrole on the surface of Fe-MIL-88B-derived 1D Fe2O3 nanorods (MIL: Material Institut Lavoisier). The Fe2O3 nanorods not only partially dissolve to generate Fe3+ for initiating polymerization but serve as templates to form the 1D structure during polymerization. Furthermore, the pyrrole coated Fe2O3 nanorod architecture prevents the porous structure from collapsing and protects Fe from aggregation to yield atomic Fe-N4 moieties during carbonization. The obtained Fe/N-CNRs display exceptional ORR activities (E1/2 = 0.90 V) and satisfactory long-term durabilities, exceeding those for Pt/C. Furthermore, the unprecedented Fe/N-CNRs catalytic performance is demonstrated with Zn-air batteries, including a superior maximum power density (181.8 mW cm−2), specific capacity (998.67 W h kg−1), and long-term durability over 100 h. The prominent performance stems from the unique 1D structure, hierarchical pore system, high surface area, and homogeneously dispersed single-atom Fe-N4 moieties.
AB - Iron-nitrogen-carbon materials are being intensively studied as the most promising substitutes for Pt-based electrocatalysts for the oxygen reduction reaction (ORR). A rational design of the morphology and porous structure can promote the accessibility of the active site and the reactants/products transportation, accelerating the reaction kinetics. Herein, 1D porous iron/nitrogen-doped carbon nanorods (Fe/N-CNRs) with a hierarchically micro/mesoporous structure are prepared by pyrolyzing the in situ polymerized pyrrole on the surface of Fe-MIL-88B-derived 1D Fe2O3 nanorods (MIL: Material Institut Lavoisier). The Fe2O3 nanorods not only partially dissolve to generate Fe3+ for initiating polymerization but serve as templates to form the 1D structure during polymerization. Furthermore, the pyrrole coated Fe2O3 nanorod architecture prevents the porous structure from collapsing and protects Fe from aggregation to yield atomic Fe-N4 moieties during carbonization. The obtained Fe/N-CNRs display exceptional ORR activities (E1/2 = 0.90 V) and satisfactory long-term durabilities, exceeding those for Pt/C. Furthermore, the unprecedented Fe/N-CNRs catalytic performance is demonstrated with Zn-air batteries, including a superior maximum power density (181.8 mW cm−2), specific capacity (998.67 W h kg−1), and long-term durability over 100 h. The prominent performance stems from the unique 1D structure, hierarchical pore system, high surface area, and homogeneously dispersed single-atom Fe-N4 moieties.
KW - 1D Fe O template
KW - Zn-air batteries
KW - atomic Fe-N sites
KW - hierarchically porous nanorods
KW - in situ polymerization
UR - http://www.scopus.com/inward/record.url?scp=85097013367&partnerID=8YFLogxK
U2 - 10.1002/adfm.202008085
DO - 10.1002/adfm.202008085
M3 - 文章
AN - SCOPUS:85097013367
SN - 1616-301X
VL - 31
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 8
M1 - 2008085
ER -