Energy Transfer between CdZnS Quantum Dots and Perylene Diimide Dyes

被引:6
|
作者
Wu, Na [1 ,2 ]
Kirkwood, Nicholas [1 ]
Neto, Nicolau Saker [1 ]
Pervin, Rehana [1 ]
Mulvaney, Paul [1 ]
Wong, Wallace W. H. [1 ]
机构
[1] Univ Melbourne, ARC Ctr Excellence Exciton Sci, Sch Chem, Parkville, Vic 3010, Australia
[2] Chinese Acad Sci, Suzhou Inst Nanotechand Nanob, Suzhou 100864, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2023年 / 127卷 / 04期
关键词
HIGHLY EFFICIENT; LIGAND-EXCHANGE; NANOCRYSTALS; SURFACE; PHOTOLUMINESCENCE; BINDING; SITES;
D O I
10.1021/acs.jpcc.3c00053
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
QD-dye systems are promising models for artificial photosynthesis and down-converter systems for LEDs and displays. To better understand the factors controlling energy transfer from the QDs to the dyes, we fabricated a series of CdxZn1-xS/ZnS quantum dot (QD)-perylene diimide (PDI) composite nanocrystals. The core-shell CdxZn1-xS/ZnS QDs were chosen for better control of surface chemistry and for the control of photophysical properties through core composition. The PDIs were designed with bulky substituents to found to depend upon both the length of the anchoring alkyl chain and the type of the terminal anchoring group. The maximum energy transfer efficiency of 91% from QDs to PDIs was achieved with composites containing PDIs with carboxylic acid anchoring groups and longer alkyl chains. It was found that composites with carboxylic acid anchors exhibited greater photostability than composites with amine anchors. Longer alkyl chains also led to greater photostability. Conversely, shorter chain alkanes promoted faster aggregation of the nanocrystal composites.
引用
收藏
页码:2116 / 2126
页数:11
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