Carbon dots bridged Zn0.5Cd0.5S with interfacial amide bond facilitating electron transfer for efficient photocatalytic hydrogen peroxide production

被引:14
作者
Tang, Ting [1 ,2 ]
Zhao, Jiwu [3 ]
Shen, Yongli [2 ]
Yang, Fan [1 ]
Yao, Shuang [2 ]
An, Changhua [1 ,2 ]
机构
[1] Tianjin Univ Technol, Sch Chem & Chem Engn, Tianjin Key Lab Organ Solar Cells & Photochem Conv, Tianjin 300384, Peoples R China
[2] Tianjin Univ Technol, Inst New Energy Mat & Low Carbon Technol, Sch Mat Sci & Engn, Tianjin Key Lab Adv Funct Porous Mat, Tianjin 300384, Peoples R China
[3] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Fujian, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 346卷
关键词
Photocatalysis; Hydrogen peroxide; Zn0.5Cd0.5S; Carbon dots; WATER;
D O I
10.1016/j.apcatb.2024.123721
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photocatalytic H2O2 production has gained significant attention as an environmentally friendly approach. The key is to explore efficient photocatalysts with sufficient active sites and excellent electron transfer capacity. Herein, we propose a novel approach by incorporating carbon dots (CDs) on ethylenediamine capped Zn0.5Cd0.5S, which was bridged with an interfacial amide bond. Smooth transfer of photoinduced electrons from Zn0.5Cd0.5S to carbon dots via a high -speed electron channel is afforded by interfacial amide bond. A remarkable H2O2 yield with a rate of 252 mu mol/h and an apparent quantum yield (AQY) of 31 % at 400 nm is achieved. Photoelectrochemical analysis and density function theory (DFT) calculation reveal CDs with abundant oxygenous functional groups as active sites, boosting activity and selectivity. This interfacial engineering strategy with the acceleration of electrons transfer and enhanced 2e selectivity can be applied to advanced photocatalytic systems for the achievement of valuable organics, environmental purification and new energy carriers.
引用
收藏
页数:8
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