CuO Nanoparticle‐Loaded TiO <sub>2</sub> Catalyst for High‐Performance Photocatalytic Hydrogen Peroxide Generation

Titanium dioxide (TiO<sub>2</sub>) has been extensively investigated in photocatalysis due to its high stability, low toxicity, and biocompatibility. However, its application in hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production is hindered by the rapid recombination of photogenerated charge carriers and the poor selectivity of the two-electron oxygen reduction reaction (2e<sup>-</sup> ORR). Here, a CuO/TiO<sub>2</sub> photocatalyst is reported, in which CuO nanoparticles are anchored on the TiO<sub>2</sub> surface as cocatalysts to provide additional active sites and promote efficient separation of photogenerated electrons and holes. The optimized CuO/TiO<sub>2</sub> exhibits a remarkable photocatalytic H<sub>2</sub>O<sub>2</sub> production rate of 19.48 mmol g<sup>-1</sup> h<sup>-1</sup>, which is 162 times higher than that of pristine TiO<sub>2</sub>, with excellent stability sustained over 7 h' continuous irradiation. The apparent quantum yield (AQY) of CuO/TiO<sub>2</sub> reaches 7.30% at 365 nm. Notably, the CuO/TiO<sub>2</sub> demonstrated the promising H<sub>2</sub>O<sub>2</sub> production in pure water (182.31 µmol g<sup>-1</sup> h<sup>-1</sup>). Femtosecond transient absorption spectra (Fs-TAS) reveal that the average lifetime of photogenerated electrons in CuO/TiO<sub>2</sub> is 5.8 times longer than in TiO<sub>2</sub>, confirming the enhanced charge separation and transfer. In situ spectroscopic analyses further demonstrate that CuO/TiO<sub>2</sub> facilitates both oxygen reduction and water oxidation pathways. These results highlight CuO/TiO<sub>2</sub> as a cost-effective and efficient photocatalyst for sustainable H<sub>2</sub>O<sub>2</sub> production.

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Journal
Small
Published
2025-11-07
DOI
https://doi.org/10.1002/smll.202510644
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73

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article

CuO Nanoparticle‐Loaded TiO 2 Catalyst for High‐Performance Photocatalytic Hydrogen Peroxide Generation

Huajie Yin, Jian Kang, Zenglong Wu, Jiangyao Chen et al.
2 citations
Small
Advanced Photocatalysis Techniques
0.73
article

CuO Nanoparticle‐Loaded TiO 2 Catalyst for High‐Performance Photocatalytic Hydrogen Peroxide Generation

Huajie Yin, Jian Kang, Zenglong Wu, Jiangyao Chen, Shijian Li, Beibei Yao, Mengfan Bi, Tengxiu Tu, Shan Chen, Zhixian Mao
article en
2 citations

Abstract

Titanium dioxide (TiO<sub>2</sub>) has been extensively investigated in photocatalysis due to its high stability, low toxicity, and biocompatibility. However, its application in hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) production is hindered by the rapid recombination of photogenerated charge carriers and the poor selectivity of the two-electron oxygen reduction reaction (2e<sup>-</sup> ORR). Here, a CuO/TiO<sub>2</sub> photocatalyst is reported, in which CuO nanoparticles are anchored on the TiO<sub>2</sub> surface as cocatalysts to provide additional active sites and promote efficient separation of photogenerated electrons and holes. The optimized CuO/TiO<sub>2</sub> exhibits a remarkable photocatalytic H<sub>2</sub>O<sub>2</sub> production rate of 19.48 mmol g<sup>-1</sup> h<sup>-1</sup>, which is 162 times higher than that of pristine TiO<sub>2</sub>, with excellent stability sustained over 7 h' continuous irradiation. The apparent quantum yield (AQY) of CuO/TiO<sub>2</sub> reaches 7.30% at 365 nm. Notably, the CuO/TiO<sub>2</sub> demonstrated the promising H<sub>2</sub>O<sub>2</sub> production in pure water (182.31 µmol g<sup>-1</sup> h<sup>-1</sup>). Femtosecond transient absorption spectra (Fs-TAS) reveal that the average lifetime of photogenerated electrons in CuO/TiO<sub>2</sub> is 5.8 times longer than in TiO<sub>2</sub>, confirming the enhanced charge separation and transfer. In situ spectroscopic analyses further demonstrate that CuO/TiO<sub>2</sub> facilitates both oxygen reduction and water oxidation pathways. These results highlight CuO/TiO<sub>2</sub> as a cost-effective and efficient photocatalyst for sustainable H<sub>2</sub>O<sub>2</sub> production.

SmallVol. 21(51)
University of Science and Technology of China (CN), Guangdong University of Technology (CN), Anhui University (CN), Hefei Institutes of Physical Science (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation
Openalex Percentile: Top 27%
Advanced Photocatalysis Techniques
0.73
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