Applied Catalysis2022,Vol.30116.DOI:10.1016/j.apcatb.2021.120765

Novel Cu-Fe bi-metal oxide quantum dots coupled g-C3N4 nanosheets with H2O2 adsorption-activation trade-off for efficient photo-Fenton catalysis

Liu, Mingen Xia, Hong Yang, Wenxin Liu, Xiaoyu Xiang, Jiao Wang, Xiaoming Hu, Liangsheng Lu, Fushen
Applied Catalysis2022,Vol.30116.DOI:10.1016/j.apcatb.2021.120765

Novel Cu-Fe bi-metal oxide quantum dots coupled g-C3N4 nanosheets with H2O2 adsorption-activation trade-off for efficient photo-Fenton catalysis

Liu, Mingen 1Xia, Hong 1Yang, Wenxin Liu, Xiaoyu Xiang, Jiao Wang, Xiaoming Hu, Liangsheng Lu, Fushen
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作者信息

  • 1. Shantou Univ, Dept Chem, Shantou 515063, Guangdong, Peoples R China
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Abstract

Exploitation of catalysts with multi-active sites is very important for enhancing catalytic performance. 0D/2D hybrids, especially quantum dots (QDs)/nanosheets (NSs), have attracted increasing attentions for advanced oxidation processes due to high charge mobility and more active sites. However, 0D/2D hybrids with multi-active sites still remain a great challenge. Herein, 0D Cu-Fe bi-metal oxide QDs/2D g-C3N4 (CNNSs) exhibiting superior advantages beyond single-metal 0D/2D counterparts was fabricated via a facile one-step synthesis strategy for photo-Fenton catalysis. The synergy of ultrafine Cu-Fe sites on CNNSs led to outstanding tetracycline removal efficiency over a wide pH range. Our experiments and DFT calculations clearly demonstrated that except for the fast charge separation and transfer, this synergy could achieve the optimal H2O2 adsorption-activation trade-off on Cu-Fe sites, while also modify tetracycline absorption, leading to multiple synergies of adsorption-catalytic degradation and photocatalysis-Fenton oxidation. This work provides new insights in developing multi-functional 0D/2D hybrids for environment and energy applications.

Key words

0D/2D hybrids/Adsorption-activation trade-off/Multiple synergies/Photo-Fenton/Wastewater treatment

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出版年

2022
Applied Catalysis

Applied Catalysis

ISSN:0926-3373
被引量56
参考文献量51
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