光催化
材料科学
金属有机骨架
载流子
复合数
分解水
超快激光光谱学
化学工程
催化作用
纳米技术
光化学
复合材料
化学
光谱学
光电子学
物理化学
吸附
量子力学
生物化学
物理
工程类
作者
Hai-Qun Xu,Sizhuo Yang,Xing Ma,Jier Huang,Hai‐Long Jiang
出处
期刊:ACS Catalysis
日期:2018-10-30
卷期号:8 (12): 11615-11621
被引量:304
标识
DOI:10.1021/acscatal.8b03233
摘要
Photocatalytic water splitting for H2 production becomes one of the most favorable pathways for solar energy utilization, while the charge-separation dynamics in composite photocatalysts is largely elusive. In the present work, CdS-decorated metal–organic framework (MOF) composites, namely, CdS/UiO-66, have been synthesized and exhibit high H2 production activity from photocatalytic water splitting, far surpassing the MOF and CdS counterparts, under visible light irradiation. Transient absorption (TA) spectroscopy has been adopted in this report to unveil the charge-separation dynamics in CdS/UiO-66 composites, a key process that dictates their function in photocatalysis. We show that, in addition to the preferable formation of fine CdS particles assisted by the MOF, effective electron transfer, which occurs from excited CdS to UiO-66, significantly inhibits the recombination of photogenerated charge carriers, ultimately boosting the photocatalytic activity for H2 generation. This report on charge-separation dynamics for CdS–MOF composites affords significant insights for future fabrication of advanced composite photocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI