Issue 9, 2024

In situ laser-assisted synthesis of MoS2 anchored on 3D porous graphene foam for enhanced alkaline hydrogen generation

Abstract

MoS2 is acknowledged as a promising alternative for Pt-based hydrogen evolution reaction (HER) catalysts, while its essential semiconductor nature and insufficient active edge sites weaken its intrinsic HER performance. Distributing MoS2 on conductive graphene is expected to enhance its conductivity and enrich its active edge sites, thus endowing it with satisfactory HER performance. Carbon-based MoS2 materials are usually fabricated via solution-based methods and thermal annealing approaches. Herein, we demonstrate in situ laser-assisted fabrication of MoS2 on laser-induced graphene (LIG) to form LIG/MoS2 electrocatalyst for HER promotion. After laser engraving on LIG with precursor solution, MoS2 is easily anchored on highly porous LIG within a few minutes in the form of nanoparticles. To afford a current density of 10 mA cm−2, LIG/MoS2 merely requires an acceptable overpotential of 130 mV in 1.0 M KOH electrolyte, which outperforms most reported carbon-related MoS2-based electrocatalysts. The impressive HER behavior is mainly ascribed to the porous structure and electrical conductivity of LIG, which respectively enriches active sites and facilitates charge transfer. This work not only offers us an attractive noble-metal-free HER promoter but opens a new route toward the facile synthesis of on-chip micro-fuel cells or catalytic microreactors.

Graphical abstract: In situ laser-assisted synthesis of MoS2 anchored on 3D porous graphene foam for enhanced alkaline hydrogen generation

Supplementary files

Article information

Article type
Paper
Submitted
16 Feb 2024
Accepted
31 Mar 2024
First published
01 Apr 2024

Catal. Sci. Technol., 2024,14, 2646-2653

In situ laser-assisted synthesis of MoS2 anchored on 3D porous graphene foam for enhanced alkaline hydrogen generation

L. Zhang, W. Fu, J. Yang, J. Yang, C. Zhou, J. Zhao and Q. Huang, Catal. Sci. Technol., 2024, 14, 2646 DOI: 10.1039/D4CY00213J

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