Issue 23, 2023

Guanosine-assisted synthesis of a core–shell Mo2N/Mo2C/C structure for enhanced hydrogen evolution reaction

Abstract

Coupling molybdenum-based materials with carbon is an effective strategy to improve the hydrogen evolution reaction (HER) performance. However, achieving the desired surface-active sites by regulating the catalyst's morphology presents a challenge. Here, we present a novel approach using guanosine as an assisting agent to synthesize core–shell Mo2N/Mo2C/C composites. By utilizing guanosine in combination with ammonium heptamolybdate, we induce the formation of new hierarchical Mo-based structures through intrinsic self-regulating mechanisms. The presence of rich interactions between guanosine molecules, such as hydrogen bonding and π–π stacking, plays a pivotal role in achieving this successful outcome. Notably, a core–shell spherical MoO2/CN polymer was formed when using an optimal amount of guanosine. By pyrolysis at 800 °C, this was transformed into the core–shell Mo2N/Mo2C/C composite. The unexpected core–shell structure was elucidated through ex situ XRD and SEM characterization, highlighting the dominance of carbon in the outer shells and molybdenum-rich phases in the core. The synthesized Mo2N/Mo2C/C composites exhibit a low overpotential of only 79 mV under alkaline conditions, which is comparable to that of commercially available Pt/C catalysts. Our study offers a promising route for developing noble-metal-free catalysts with enhanced HER performance, contributing to the advancement of green hydrogen generation technologies.

Graphical abstract: Guanosine-assisted synthesis of a core–shell Mo2N/Mo2C/C structure for enhanced hydrogen evolution reaction

Supplementary files

Article information

Article type
Research Article
Submitted
24 Jul 2023
Accepted
28 Sep 2023
First published
28 Sep 2023

Inorg. Chem. Front., 2023,10, 7018-7027

Guanosine-assisted synthesis of a core–shell Mo2N/Mo2C/C structure for enhanced hydrogen evolution reaction

M. Xia, S. Li, X. Zhang and Z. Xie, Inorg. Chem. Front., 2023, 10, 7018 DOI: 10.1039/D3QI01420G

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