纳米棒
催化作用
可见光谱
材料科学
分解水
纳米颗粒
光诱导电荷分离
光催化分解水
化学工程
纳米晶
光催化
光化学
纳米技术
光电子学
人工光合作用
化学
工程类
生物化学
作者
Christian Wolff,Peter D. Frischmann,Marcus Schulze,Bernhard J. Bohn,Robin Wein,Panajotis Livadas,Michael T. Carlson,Frank Jäckel,Jochen Feldmann,Frank Würthner,Jacek K. Stolarczyk
出处
期刊:Nature Energy
[Springer Nature]
日期:2018-08-29
卷期号:3 (10): 862-869
被引量:415
标识
DOI:10.1038/s41560-018-0229-6
摘要
Full water splitting into hydrogen and oxygen on semiconductor nanocrystals is a challenging task; overpotentials must be overcome for both half-reactions and different catalytic sites are needed to facilitate them. Additionally, efficient charge separation and prevention of back reactions are necessary. Here, we report simultaneous H-2 and O-2 evolution by CdS nanorods decorated with nanoparticulate reduction and molecular oxidation co-catalysts. The process proceeds entirely without sacrificial agents and relies on the nanorod morphology of CdS to spatially separate the reduction and oxidation sites. Hydrogen is generated on Pt nanoparticles grown at the nanorod tips, while Ru(tpy)(bpy)Cl-2-based oxidation catalysts are anchored through dithiocarbamate bonds onto the sides of the nanorod. O-2 generation from water was verified by O-18 isotope labelling experiments, and time-resolved spectroscopic results confirmed efficient charge separation and ultrafast electron and hole transfer to the reaction sites. The system demonstrates that combining nanoparticulate and molecular catalysts on anisotropic nanocrystals provides an effective pathway for visible-light-driven photocatalytic water splitting.
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