催化作用
吸附
光催化
氧化物
材料科学
量子点
化学工程
协同催化
降级(电信)
化学
纳米技术
光化学
金属
有机化学
冶金
电信
工程类
计算机科学
作者
Mingen Liu,Hong Xia,Wenxin Yang,Xiaoyu Liu,Jiao Xiang,Xiaoming Wang,Liangsheng Hu,Fushen Lu
标识
DOI:10.1016/j.apcatb.2021.120765
摘要
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.
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