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Efficient and Reabsorption‐Free Radioluminescence in Cs3Cu2I5 Nanocrystals with Self‐Trapped Excitons.

Authors :
Lian, Linyuan
Zheng, Moyan
Zhang, Weizhuo
Yin, Lixiao
Du, Xinyuan
Zhang, Peng
Zhang, Xiuwen
Gao, Jianbo
Zhang, Daoli
Gao, Liang
Niu, Guangda
Song, Haisheng
Chen, Rong
Lan, Xinzheng
Tang, Jiang
Zhang, Jianbing
Source :
Advanced Science. Jun2020, Vol. 7 Issue 11, p1-9. 9p.
Publication Year :
2020

Abstract

Radioluminescent materials (scintillators) are widely applied in medical imaging, nondestructive testing, security inspection, nuclear and radiation industries, and scientific research. Recently, all‐inorganic lead halide perovskite nanocrystal (NC) scintillators have attracted great attention due to their facile solution processability and ultrasensitive X‐ray detection, which allows for large area and flexible X‐ray imaging. However, the light yield of these perovskite NCs is relatively low because of the strong self‐absorption that reduces the light out‐coupling efficiency. Here, NCs with self‐trapped excitons emission are demonstrated to be sensitive, reabsorption‐free scintillators. Highly luminescent and stable Cs3Cu2I5 NCs with a photoluminescence quantum yields of 73.7%, which is a new record for blue emission lead‐free perovskite or perovskite‐like NCs, is produced with the assistance of InI3. The PL peak of the Cs3Cu2I5 NCs locates at 445 nm that matches with the response peak of a silicon photomultiplier. Thus, Cs3Cu2I5 NCs are demonstrated as efficient scintillators with zero self‐absorption and extremely high light yield (≈79 279 photons per MeV). Both Cs3Cu2I5 NC colloidal solution and film exhibit strong radioluminescence under X‐ray irradiation. The potential application of Cs3Cu2I5 NCs as reabsorption‐free, low cost, large area, and flexible scintillators is demonstrated by a prototype X‐ray imaging with a high spatial resolution. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21983844
Volume :
7
Issue :
11
Database :
Academic Search Index
Journal :
Advanced Science
Publication Type :
Academic Journal
Accession number :
143703898
Full Text :
https://doi.org/10.1002/advs.202000195