Electronic structure optimization with heterointerface design in heteroatom-doped carbon-supported MoO2/Au–MoS2 composites for multifunctional catalysis

Abstract

It is advantageous to harness the synergistic effect of multiple components to enhance the catalytic performance of integrated nanozymes, mimicking the efficacy of natural enzymes in catalytic processes. Herein, the enzyme-like catalysis of a three-dimensional (3D) Au-decorated MoS2 nanosheets (NSs) grown in situ on S, N, P, and Fe-doped carbon@MoO2 substrate derived from rod-like structured MoO3@Fe-PZS is investigated. Compared with single MoS2 NSs, the synergistic effects of Au nanoparticle (NP) decoration, S, N, P, and Fe-doped carbon@MoO2 substrate and 1D open porous structural advantages allow Au–MoS2/Fe-NPSC@MoO2 to achieve optimum enzyme-like activity as well as the reduction of 4-nitrophenol(4-NP). In addition, good hydrophilicity of Au–MoS2/Fe-NPSC@MoO2 is conducive to achieving rapid mass transport. The test results showed that the composite exhibited excellent peroxidase activity and 4-NP catalytic reduction performance thanks to the synergistic effect of the above components. Therefore, Au–MoS2/Fe-NPSC@MoO2 composites have great potential in the development of artificial enzymes with catalytic dynamics of natural enzymes. This research introduces a facile approach for concurrently incorporating structural merits, electrical conductivity, and electronic engineering principles to develop versatile catalyst systems with multifaceted functionalities.

Graphical abstract: Electronic structure optimization with heterointerface design in heteroatom-doped carbon-supported MoO2/Au–MoS2 composites for multifunctional catalysis

Supplementary files

Article information

Article type
Paper
Submitted
27 Aug 2025
Accepted
13 Oct 2025
First published
14 Oct 2025

CrystEngComm, 2025, Advance Article

Electronic structure optimization with heterointerface design in heteroatom-doped carbon-supported MoO2/Au–MoS2 composites for multifunctional catalysis

T. Sun, S. Xie, L. Chen, J. Xu, X. Yin and M. Zhang, CrystEngComm, 2025, Advance Article , DOI: 10.1039/D5CE00834D

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