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Discovering New Type of Lead‐Free Cluster‐Based Hybrid Double Perovskite Derivatives with Chiral Optical Activities and Low X‐Ray Detection Limit.

Authors :
Zhu, Zeng‐Kui
Zhu, Tingting
Wu, Jianbo
You, Shihai
Yu, Panpan
Liu, Xitao
Li, Lina
Ji, Chengmin
Luo, Junhua
Source :
Advanced Functional Materials; 6/26/2023, Vol. 33 Issue 26, p1-8, 8p
Publication Year :
2023

Abstract

2D chiral hybrid perovskites have recently emerged as outstanding semiconductor materials. However, most of the reported 2D chiral perovskites have limited structural types and contain high levels of toxic lead, which severely hinders their further applications. Herein, by using a mixed‐cation strategy, an unprecedented type of lead‐free cluster‐based 2D chiral hybrid double perovskite derivatives are successfully obtained, [(R/S‐PPA)4(IPA)6Ag2Bi4I24]·2H2O (1‐R and 1‐S), and [(R/S‐PPA)4(n‐BA)6Ag2Bi4I24]·2H2O (2‐R and 2‐S) (R/S‐PPA=R/S–1‐phenylpropylamine; IPA=isopentylamine; n‐BA=n‐butylamine). Their inorganic skeletons are linked by binuclear {Bi2I10} and infinite chain {Ag2Bi2I14}∞, in which bismuth clusters and multiple coordination modes (e.g., tetrahedral AgI4 and octahedral AgI6) are introduced into the double perovskite system for the first time. This introduction induces distortion of the inorganic layer, which may facilitate the transfer of chirality from the chiral cations into achiral double perovskite skeletons. Further, circular dichroism measurements and circularly polarized light detection confirm their inherent chiral optical activities. In addition, 1‐S exhibits an ultralow X‐ray detection limit of 129.5 nGy s−1, which is 42‐fold lower than that of demands in regular medical diagnosis (5.5 µGy s−1). This study provides a pathway to construct novel type of lead‐free cluster‐based double perovskite derivatives. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
33
Issue :
26
Database :
Complementary Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
164587600
Full Text :
https://doi.org/10.1002/adfm.202214660