Bright State Sensitized Triplet Energy Transfer from Quantum Dot to Molecular Acceptor Revealed by Temperature Dependent Energy Transfer Dynamics

被引:18
|
作者
Jin, Tao [1 ]
He, Sheng [1 ]
Zhu, Yifan [2 ]
Egap, Eilaf [2 ,3 ]
Lian, Tianquan [1 ]
机构
[1] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
[2] Rice Univ, Dept Mat Sci & NanoEngn, Houston, TX 77005 USA
[3] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
基金
美国国家科学基金会;
关键词
quantum dot; triplet energy transfer; exciton fine structure; transient absorption; spectroscopy; EXCITATION TRANSFER; CDSE NANOCRYSTALS; RATE EXPRESSIONS; DARK-EXCITON; LUMINESCENCE; DECAY;
D O I
10.1021/acs.nanolett.2c00017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantum dot (QD) sensitized molecular triplet excited state generation has been a promising alternative for traditional triplet state harvesting schemes. However, the correlation between QD bright/dark states and QD sensitized triplet energy transfer (TET) has been unclear. Herein, we studied the bright/dark states contribution to TET with CdSe/CdS core/shell QD-oligothiophene as the model system. Equilibrium between QD bright and dark states was tuned by changing temperature, and TET dynamics were monitored with transient absorption spectroscopy. Analysis of acceptor triplet excited state growth kinetics yields rates of TET from bright and dark states as 0.492 +/- 0.011 ns(-1) and 0.0271 +/- 0.0014 ns(-1) at 5 K, suggesting significant contribution of bright states to TET. The result was rationalized by bright state wave function components with the same electron/hole spin projections leading to nonzero TET probability. The study provides new insights into QD sensitized TET mechanisms and inspiration for future TET efficiency optimization through QD exciton engineering.
引用
收藏
页码:3897 / 3903
页数:7
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