Intraband Transitions of Nanocrystals Transforming from Lead Selenide to Self-doped Silver Selenide Quantum Dots by Cation Exchange

被引:17
作者
Bera, Rajesh [1 ,2 ]
Choi, Dongsun [1 ]
Jung, Yoon Seo [1 ]
Song, Haemin [1 ]
Jeong, Kwang Seob [1 ,2 ]
机构
[1] Korea Univ, Dept Chem, Seoul 02841, South Korea
[2] Korea Univ, Ctr Mol Spect & Dynam, Inst Basic Sci IBS, Seoul 02841, South Korea
基金
新加坡国家研究基金会;
关键词
FILMS;
D O I
10.1021/acs.jpclett.2c01179
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
In search of heavy metal-free mid-IR active colloidal materials, selfdoped silver selenide colloidal quantum dots (CQDs) can be an alternative offering tunable mid-IR wavelength with a narrow bandwidth. One of the challenges in the study of the intraband transition is developing a method to widen the intraband transition energy range as well as reducing the toxicity of the materials. Here, we present AgxSe (x > 2) CQDs exhibiting an intraband transition up to 0.39 eV, produced by the cation exchange (CE) method from PbSe CQDs. The major electronic transition efficiently changes from the SWIR band gap of PbSe CQDs to the mid-IR intraband transition of the AgxSe CQDs by the CE. The intraband exciton is verified by examining the absorption and emission of the CE AgxSe CQDs as well as their applications on electrochemical mid-IR luminescence and mid-IR intraband photodetectors.
引用
收藏
页码:6138 / 6146
页数:9
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