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Research Article | Open Access

Dual-plasmonic CuxSbyS/Cu heteronanostructures: Efficient photocatalysts for ammonia borane methanolysis dehydrogenation

Guoning Liu1,§ ( ), Dan Wang1,§, Yihe Zhu1, Chaonan Zeng1, Yujin Li1( ), Shaopeng Qi2,3, Chongyi Ling4, Xiuyun Zhang5
Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, School of Chemistry and Chemical Engineering, Huaibei Normal University, Huaibei 235000, China
School of Mechanical and Electrical Engineering, Chizhou University, Chizhou 247000, China
School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Key Laboratory of Quantum Materials and Devices of Ministry of Education, School of Physics, Southeast University, Nanjing 211189, China
College of Physics Science and Technology, Yangzhou University, Yangzhou 225002, China

§ Guoning Liu and Dan Wang contributed equally to this work.

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Abstract

Plasmonic nanotubes are promising for photocatalysis due to their hollow structure, strong light–matter coupling, enhanced scattering, short charge paths, and abundant active sites. However, their synthesis is challenging, with few reports. Uniform CuxSbyS nanotubes and CuxSbyS/Cu dual-plasmonic heteronanostructures were synthesized via direct colloidal hot-injection by controlling reaction parameters. In ammonia borane methanol dehydrogenation, the heterostructure achieves a hydrogen production rate (690.17 mmolH2⋅gcat−1⋅h−1) 5.5× higher than CuxSbyS nanotubes (126.21 mmolH2⋅gcat−1⋅h−1) and 198.9× that of Cu nanoparticles (3.47 mmolH2⋅gcat−1⋅h−1), demonstrating stability over 10 cycles. Synergistic effects drive activity: Hollow structure improves light harvesting and surface exposure; CuxSbyS/Cu interface enables charge separation and transfer, reducing recombination; strong plasmonic absorption enhances photon utilization. Results confirm electron transfer from CuxSbyS to Cu, stabilizing nanoparticles and improving durability. Density functional theory identifies CH3OBH2NH3 desorption (not O–H cleavage) as the rate-determining step, offering new mechanistic insight. This method enables applications in solar hydrogen production, environmental purification, and energy-efficient conversion for sustainable energy and green chemistry.

Graphical Abstract

Uniform CuxSbyS/Cu dual-plasmonic heteronanostructures synthesized by colloidal hot-injection show enhanced hydrogen production in ammonia borane methanolysis, maintaining stability. Results confirm electron transfer from CuxSbyS to Cu, enabling efficient charge separation, reduced recombination, and improved stability. Density functional theory (DFT) identifies CH3OBH2NH3 desorption, not O–H cleavage, as the rate-determining step, offering key mechanistic insights.

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Nano Research
Article number: 94908963

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Cite this article:
Liu G, Wang D, Zhu Y, et al. Dual-plasmonic CuxSbyS/Cu heteronanostructures: Efficient photocatalysts for ammonia borane methanolysis dehydrogenation. Nano Research, 2026, 19(12): 94908963. https://doi.org/10.26599/NR.2026.94908963

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Received: 28 December 2025
Accepted: 22 June 2026
Published: 21 September 2026
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).