Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/182935
Title: Anchoring AuCu alloy nanoparticles on TiO2 nanosheets: exploiting synergistic effects and directed electron transfer for enhanced photocatalytic H2 evolution
Authors: Zhao, Yahao
Ye, Furong
Han, Changcun
Liu, Peng
Liu, Wen
Huang, Yizhong
Chen, Xupeng
Tian, Jiayi
Keywords: Engineering
Issue Date: 2025
Source: Zhao, Y., Ye, F., Han, C., Liu, P., Liu, W., Huang, Y., Chen, X. & Tian, J. (2025). Anchoring AuCu alloy nanoparticles on TiO2 nanosheets: exploiting synergistic effects and directed electron transfer for enhanced photocatalytic H2 evolution. Ceramics International, 51(1), 940-948. https://dx.doi.org/10.1016/j.ceramint.2024.11.077
Journal: Ceramics International
Abstract: AuCu/TiO2 composite photocatalysts were prepared by anchoring AuCu nanoparticles (NPs) on TiO2 nanosheets using a simple photoreduction method. Visible diffuse reflectance spectra indicated that the AuCu/TiO2 significantly enhanced light absorption in the visible region. Through photoluminescence spectroscopy and steady-state surface photovoltage experiments, AuCu/TiO2 exhibits an excellent photogenerated electron transfer rate. In addition, photoelectrochemical experiments showed that AuCu/TiO2 had a high photogenerated charge separation efficiency. AuCu/TiO2 (1.0 wt%) exhibited the best performance, under full spectrum, the hydrogen evolution rate is 33.94 mmol g−1 h−1, which is 1.59 times and 1.66 times higher than that of single metal Au/TiO2 (1.0 wt%) (21.28 mmol g−1 h−1) and Cu/TiO2 (1.0 wt%) (20.42 mmol g−1 h−1), respectively. The results showed that AuCu NPs greatly enhanced the photocatalytic performance of the composite photocatalysts.
URI: https://hdl.handle.net/10356/182935
ISSN: 0272-8842
DOI: 10.1016/j.ceramint.2024.11.077
Schools: School of Materials Science and Engineering 
Rights: © 2024 Elsevier Ltd and Techna Group S.r.l. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MSE Journal Articles

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