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Carbon nanotube supported zinc, cobalt, nitrogen, sulfur-doped porous carbon as electrocatalyst for enhanced oxygen reduction reaction.

Authors :
Gao, Haili
Zhao, Jingfang
Ma, Yaqiong
Liu, Yunpeng
Zhang, Yong
Zhang, Linsen
Yin, Zhigang
Source :
International Journal of Hydrogen Energy. Jan2024:Part B, Vol. 51, p1229-1241. 13p.
Publication Year :
2024

Abstract

Carbon nanotube (CNT) supported zinc, cobalt, nitrogen, sulfur-doped porous carbon (CNT@ZnCo/NSC) catalysts are prepared by in situ growth of sulfur-containing bimetal zeolitic imidazolate framework (S–ZnCo-ZIF) polyhedrons on CNT with subsequent heat treatment. The microstructure, morphology, particle size distribution, specific surface area, and pore-size distribution of the catalysts are characterized by multiple techniques. CNT@ZnCo/NSC exhibits excellent catalytic activity for oxygen reduction reaction (ORR) with onset potential of 0.98 V and half-wave potential of 0.83 V, respectively, which are close to those of Pt/C. The addition of CNT inhibits the agglomeration and improves the conductivity of the catalysts, while S doping enhances the electrochemical surface area and introduces active sites. The special structure makes CNT@ZnCo/NSC possess proper specific surface area (390.8 m2 g−1) and large average pore size (5.26 nm). CNT@ZnCo/NSC contains more graphite-N (21%) and pyridine-N (55.9%) than CNT@ZnCo/NC (20%, 46.5%) and ZnCo/NC (8.2%, 45.8%). CNT@ZnCo/NSC catalyst has better methanol tolerance and long-term stability than commercial Pt/C. [Display omitted] • CNT supported Zn, Co, N, S-doped carbon are prepared by heating of S–ZnCo-ZIF/CNT. • CNT inhibits the agglomeration and improves the conductivity of CNT@ZnCo/NSC. • S doping enhances the ECSA of CNT@ZnCo/NSC and introduces active sites. • CNT@ZnCo/NSC exhibits excellent catalytic activity for ORR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
51
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
174321084
Full Text :
https://doi.org/10.1016/j.ijhydene.2023.09.144