TY - JOUR
T1 - Sterically Suppressed Phase Segregation in 3D Hollow Mixed-Halide Wide Band Gap Perovskites
AU - Grater, Luke
AU - Wang, Mingcong
AU - Teale, Sam
AU - Mahesh, Suhas
AU - Maxwell, Aidan
AU - Liu, Yanjiang
AU - Park, So Min
AU - Chen, Bin
AU - Laquai, Frédéric
AU - Kanatzidis, Mercouri G.
AU - Sargent, E.
N1 - KAUST Repository Item: Exported on 2023-07-11
Acknowledged KAUST grant number(s): OSR-2020-CRG9-4350, OSR-2019-CRG8-4093, OSR-CARF/CCF-3079
Acknowledgements: This research was made possible by the U.S. Department of the Navy, Office of Naval Research (grant N00014-20-1-2572). M.G.K. was supported in part by grant SC0012541 from the U.S. Department of Energy, Office of Science. This publication is based upon work supported by the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) under Award No: OSR-CARF/CCF-3079, OSR-2019-CRG8-4093, and OSR-2020-CRG9-4350. L.G. thanks the University of Toronto CSICOMP NMR Facility for their assistance with 1H NMR characterization.
PY - 2023/6/27
Y1 - 2023/6/27
N2 - Band gap tuning in mixed-halide perovskites enables efficient multijunction solar cells and LEDs. However, these wide band gap perovskites, which contain a mixture of iodide and bromide ions, are known to phase segregate under illumination, introducing voltage losses that limit stability. Previous studies have employed inorganic perovskites, halide alloys, and grain/interface passivation to minimize halide segregation, yet photostability can be further advanced. By focusing on the role of halide vacancies in anion migration, one expects to be able to erect local barriers to ion migration. To achieve this, we employ a 3D "hollow" perovskite structure, wherein a molecule that is otherwise too large for the perovskite lattice is incorporated. The amount of hollowing agent, ethane-1,2-diammonium dihydroiodide (EDA), varies the density of the hollow sites. Photoluminescence measurements reveal that 1% EDA in the perovskite bulk can stabilize a 40% bromine mixed-halide perovskite at 1 sun illumination intensity. These, along with capacitance-frequency measurements, suggest that hollow sites limit the mobility of the halide vacancies.
AB - Band gap tuning in mixed-halide perovskites enables efficient multijunction solar cells and LEDs. However, these wide band gap perovskites, which contain a mixture of iodide and bromide ions, are known to phase segregate under illumination, introducing voltage losses that limit stability. Previous studies have employed inorganic perovskites, halide alloys, and grain/interface passivation to minimize halide segregation, yet photostability can be further advanced. By focusing on the role of halide vacancies in anion migration, one expects to be able to erect local barriers to ion migration. To achieve this, we employ a 3D "hollow" perovskite structure, wherein a molecule that is otherwise too large for the perovskite lattice is incorporated. The amount of hollowing agent, ethane-1,2-diammonium dihydroiodide (EDA), varies the density of the hollow sites. Photoluminescence measurements reveal that 1% EDA in the perovskite bulk can stabilize a 40% bromine mixed-halide perovskite at 1 sun illumination intensity. These, along with capacitance-frequency measurements, suggest that hollow sites limit the mobility of the halide vacancies.
UR - http://hdl.handle.net/10754/692877
UR - https://pubs.acs.org/doi/10.1021/acs.jpclett.3c01156
U2 - 10.1021/acs.jpclett.3c01156
DO - 10.1021/acs.jpclett.3c01156
M3 - Article
C2 - 37368406
SN - 1948-7185
SP - 6157
EP - 6162
JO - The Journal of Physical Chemistry Letters
JF - The Journal of Physical Chemistry Letters
ER -