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Enhanced photoluminescence and reduced dimensionality via vacancy ordering in a 10H halide perovskite

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Liu_2023_IC_Enhanced_photoluminescence_CC.pdf (3.866Mb)
Date
13/02/2023
Author
Liu, Hang
Hafeez, Hassan
Cordes, David B.
Slawin, Alexandra M. Z.
Peters, Gavin
Lee, Steve
Samuel, Ifor D. W.
Morrison, Finlay D.
Funder
EPSRC
EPSRC
Grant ID
EP/R023751/1
EP/T019298/1
Keywords
QD Chemistry
DAS
MCP
Metadata
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Abstract
Vacancy-ordered halide perovskites have received great interest in optoelectronic applications. In this work, we report the novel inorganic halide Cs10MnSb6Cl30 with a distinctive 10H (10-layer hexagonal) perovskite polytype structure with (hcccc)2 stacking. Cs10MnSb6Cl30 has 30% B-site vacancies ordered at both corner- and face-sharing sites, resulting in [MnSb6Cl30]10–n columns, i.e., a reduction of octahedral connectivity to 1D. This results in enhanced photoluminescence in comparison to the previously reported 25% vacancy-ordered 3C polytype Cs4MnSb2Cl12 with 2D connectivity. This demonstrates not only the existence of the 10H perovskite structure in halides but also demonstrates the degree of B-site deficiency and stacking sequence variation as a direction to tune the optical properties of perovskite polytypes via vacancy rearrangements.
Citation
Liu , H , Hafeez , H , Cordes , D B , Slawin , A M Z , Peters , G , Lee , S , Samuel , I D W & Morrison , F D 2023 , ' Enhanced photoluminescence and reduced dimensionality via vacancy ordering in a 10H halide perovskite ' , Inorganic Chemistry . https://doi.org/10.1021/acs.inorgchem.2c04433
Publication
Inorganic Chemistry
Status
Peer reviewed
DOI
https://doi.org/10.1021/acs.inorgchem.2c04433
ISSN
0020-1669
Type
Journal article
Rights
Copyright © 2023 The Authors. This work has been made available online in accordance with publisher policies or with permission. Permission for further reuse of this content should be sought from the publisher or the rights holder. This is the final published version of the work, which was originally published at https://doi.org/10.1021/acs.inorgchem.2c04433.
Description
H.L. would like to thank the University of St. Andrews for financial support via a St. Leonard’s scholarship. The authors acknowledge facilities access made possible through support from the EPSRC Light Element Analysis facility Grant EP/T019298/1 and the EPSRC Strategic Equipment Resource Grant EP/R023751/1.
Collections
  • University of St Andrews Research
URI
http://hdl.handle.net/10023/26977

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