光催化
量子点
制氢
光化学
载流子
材料科学
电子转移
化学
催化作用
纳米技术
光电子学
有机化学
作者
Siman Mao,Yajun Zou,Guotai Sun,Lingzhen Zeng,Zhiye Wang,Dandan Ma,Ying Guo,Yonghong Cheng,Cheng Wang,Jian‐Wen Shi
标识
DOI:10.1016/j.jcis.2020.07.121
摘要
Abstract Metal-organic frameworks (MOFs)/semiconductor hybrids have attracted attention in photocatalysis. Herein, we report a new strategy to use thiol-laced UiO-66 (UiO-66-(SH)2) as a porous and functional support for anchoring CdS quantum dots (QDs) (size: 0.5/3 nm). Cd2+ ions are firstly absorbed into the cavities of UiO-66-(SH)2 MOFs via coordinating to the thiol groups in the presence of a base to produce UiO-66-(S-Cd)2, then thiourea is added to form UiO-66-(S-CdS)2 (abbreviated as UiOS-CdS). It is clearly revealed by ultrafast transient absorption spectroscopy that the thio linkage between UiO-66 and CdS acts as an effective transfer bridge of charge carriers, which greatly promotes the interface transfer process of photogenerated electrons and holes, boosting the photocatalytic hydrogen production performance from water splitting. The optimized UiOS-CdS exhibits a photocatalytic H2 production rate of 153.2 μmol h−1 (10 mg of catalyst) under visible-light irradiation (λ > 420 nm) in the absence of nobel metal co-catalyst, corrsponding to an apparent quantum efficiency of 11.9% at 420 nm. This work may provide an effective strategy to construct QDs-linker-MOFs stylephotocatalysts for efficient energy conversion.
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