光催化
电子转移
量子产额
酰胺
乙二胺
选择性
量子点
密度泛函理论
材料科学
光化学
化学
纳米技术
催化作用
有机化学
计算化学
物理
荧光
量子力学
作者
Ting Tang,Jiwu Zhao,Yongli Shen,Jing Wang,Shuang Yao,Changhua An
标识
DOI:10.1016/j.apcatb.2024.123721
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 μmol/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.
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