Melamine-assisted synthesis of ultrafine Mo2C/Mo2N@N-doped carbon nanofibers for enhanced alkaline hydrogen evolution reaction activity

Publication Name

Science China Materials

Abstract

Noble metal-free electrocatalysts with high activity are highly desirable for the large-scale application of hydrogen evolution reaction (HER). Mo C-based nanomaterials have been proved as a promising alternative to noble metal-based electrocatalysts owing to the Pt-resembled d-band density and optimal intermediates-adsorption properties. However, the aggregation and excessive growth of crystals often occur during their high-temperature synthesis procedure, leading to low catalytic utilization. In this study, the ultrafine Mo C/Mo N heterostructure with large surface and interface confined in the N-doped carbon nanofibers (N-CNFs) was obtained by a melamine-assisted method. The synergistic effect of Mo C/Mo N heterostructure and plenty active sites exposed on the surface of ultrafine nanocrystals improves the electrocatalytic activity. Meanwhile, the N-CNFs ensure fast charge transfer and high structural stability during reactions. Moreover, the in-situ synthesis method strengthens the interfacial coupling interactions between Mo C/Mo N heterostructure and N-CNFs, further enhancing the electronic conductivity and electrocatalytic activity. Owing to these advantages, Mo C/Mo N@N-CNFs exhibit excellent HER performance with a low overpotential of 75 mV at a current density of 10 mV cm in alkaline solution, superior to the single phased Mo C counterpart and recently reported Mo C/Mo N based catalysts. This study highlights a new effective strategy to design efficient electrocatalysts via integrating heterostructure, nanostructure and carbon modification. 2 2 2 2 2 2 2 2 2 2 2 2 −2

Open Access Status

This publication may be available as open access

Volume

64

Issue

5

First Page

1150

Last Page

1158

Funding Number

51572299

Funding Sponsor

National Natural Science Foundation of China

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Link to publisher version (DOI)

http://dx.doi.org/10.1007/s40843-020-1511-7