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Fabrication of Mo2C nanoparticles on N-doped carbon nanosheets as high-performance electrocatalyst.

Authors :
Sun, Jingjing
Chen, Xiaojun
Mao, Ziyao
Liu, Bichan
Zhao, Ruihua
Du, Jianping
Source :
Journal of Alloys & Compounds. Feb2023, Vol. 934, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Molybdenum carbide is a promising material as electrocatalyst for hydrogen evolution reaction (HER). Herein, a facile strategy was proposed to prepare Mo-precursor by coordination of Mo with polysaccharide from natural biomass (jujube) at room temperature, which also acted as carbon and chelating agent. After the Mo-polysaccharide complex is carbonized, Mo 2 C nanoparticles (NPs) are highly dispersed on N-doped carbon matrix. In this process, nitrogen self-doping, lamellar carbon formation and molybdenum carbonization were achieved simultaneously, and particle aggregation is avoided. The results show that 2D carbon nanosheets-embedded Mo 2 C NPs is an excellent electrocatalyst for HER in alkaline medium. An overpotential of 124 mV at j = 10 mA cm−2 can be reached when the optimum Mo 2 C/NC-1.0 material as electrode material, and it is better than other Mo 2 C materials reported recently. The exceptional HER performance is originated from the 2D lamellar structure and rich-N atom from jujube source, which can accelerate electron transfer and change the electron density of Mo 2 C. This study opens a new avenue to design biomass-derived C/Mo 2 C used as catalyst in hydrogen-evolving reactions. [Display omitted] • Polysaccharide from jujube acts as chelating agent and provides anchor point of Mo. • Nitrogen self-doping and formation of carbon nanosheets/Mo 2 C was achieved in-situ. • The as-obtained Mo 2 C/NC exhibited exceptional HER electrocatalytic performance. • Jujube-derived C/Mo 2 C is a promising non-noble metal catalyst for energy applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
934
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
160581951
Full Text :
https://doi.org/10.1016/j.jallcom.2022.167931