期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 13, 页码 4789-4796出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b12976
关键词
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资金
- Ministry of Science and Technology of China [2013CB834505, 2014CB239402, 2013CB834804]
- National Natural Science Foundation of China [91027041, 21390404, 21603248, 51373193]
- Strategic Priority Research Program of the Chinese Academy of Science [XDB17030300]
- Chinese Academy of Sciences
- DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]
Colloidal quantum dots (QDs) have demonstrated great promise in artificial photosynthesis. However, the ultrasmall size hinders its controllable and effective interaction with cocatalysts. To improve the poor interparticle electronic communication between free QD and cocatalyst, we design here a self-assembled architecture of nanoparticles, QDs and Pt nanoparticles, simply jointed together by molecular polyacrylate to greatly enhance the rate and efficiency of interfacial electron transfer (ET). The enhanced interparticle electronic communication is confirmed by femtosecond transient absorption spectroscopy and X-ray transient absorption. Taking advantage of the enhanced interparticle ET with a time scale of similar to 65 ps, 5.0 mL of assembled CdSe/CdS QDs/cocatalysts solution produces 94 +/- 1.5 mL (4183 +/- 67 mu mol) of molecular H-2 in 8 h, giving rise to an internal quantum yield of similar to 65% in the first 30 min and a total turnover number of >1.64 x 10(7) per Pt nanoparticle. This study demonstrates that self-assembly is a promising way to improve the sluggish kinetics of the interparticle ET process, which is the key step for advanced H2 photosynthesis.
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