Ultrafast intraband Auger process in self-doped colloidal quantum dots

被引:10
|
作者
Lim, Joonhyung [1 ,2 ]
Choi, Yun Chang [2 ]
Choi, Dongsun [1 ,2 ]
Chang, I-Ya [3 ]
Hyeon-Deuk, Kim [3 ]
Jeong, Kwang Seob [1 ,2 ]
Kwak, Kyungwon [1 ,2 ]
Cho, Minhaeng [1 ,2 ]
机构
[1] Korea Univ, Ctr Mol Spect & Dynam, Inst Basic Sci IBS, Seoul 02841, South Korea
[2] Korea Univ, Dept Chem, Seoul 02841, South Korea
[3] Kyoto Univ, Dept Chem, Kyoto 6068502, Japan
基金
日本学术振兴会;
关键词
electronic-to-vibrational energy transfer; EVET; femtosecond IR pump-probe spectroscopy; infrared nanomaterials; intraband auger process; MAP1: Discovery; self-doped quantum dots;
D O I
10.1016/j.matt.2020.12.026
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Investigating the separate dynamics of electrons and holes has been challenging, although it is critical for the fundamental understanding of semiconducting nanomaterials. n-Type self-doped colloidal quantum dots (CQDs) with excess electrons occupying the low-lying state in the conduction band (CB) have attracted a great deal of attention because of not only their potential applications to infrared optoelectronics but also their intrinsic system that offers a platform for investigating electron dynamics without elusive contributions from holes in the valence band. Here, we show an unprecedented ultrafast intraband Auger process, electron relaxation between spin orbit coupling states, and exciton-to-ligand vibrational energy transfer process that all occur exclusively in the CB of the self-doped beta-HgS CQDs. The electron dynamics obtained by femtosecond mid infrared spectroscopy will pave the way for further understanding of the blinking phenomenon, disproportionate charging in light-emitting diodes, and hot electron dynamics in higher quantum states coupled to surface states of CQDs.
引用
收藏
页码:1072 / 1086
页数:15
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