材料科学
纳米反应器
贵金属
化学工程
三元运算
异质结
纳米技术
纳米点
量子点
纳米颗粒
可见光谱
金属
光催化
催化作用
光化学
化学
光电子学
有机化学
工程类
冶金
程序设计语言
计算机科学
作者
Xiang‐Bin Meng,Jing‐Li Sheng,Hong‐Liang Tang,Xiaojun Sun,Hong Dong,Fengming Zhang
标识
DOI:10.1016/j.apcatb.2018.11.018
摘要
Avoiding the utilization of noble-metal cocatalyst and the aggregation of nano photocatalysts in the preparation and photocatalytic reaction are two important aspects in the area of photocatalytic H2 evolution. In this work, for the first time, CdS quantum dots and carbon nanodots (CDs) were successfully co-immobilized in the cages of MIL-101 by one-step double solvents method followed by heating treatment. The optimum photocatalytic H2-evolution rate of CD/[email protected](50) composite with CDs content of 5.2 wt% exhibits a H2 evolution rate of 14.66 μmol h−1 without noble metal assisted under visible-light irradiation, which is 8.5 and 18.6 times higher than that of [email protected] and bare CdS, respectively. The improved photocatalytic H2-production activity of CD/[email protected] ternary composite is predominantly attributed to the effect of CDs, which mainly serves as an electron collector to efficiently prolong the lifetime of the photogenerated charge carriers from [email protected] heterostructure. This work provide a new strategy of one-step double solvents method to co-incorporate two functional species to the pores of metal-organic frameworks (MOFs) to improve the photocatalytic H2 evolution activity of host photocatalyst.
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