Dimethylammonium: An A‐site Cation for Modifying CsPbI3

All‐inorganic perovskite materials are attractive alternatives to organic‐inorganic perovskites because of their potential for higher thermal stability. While CsPbI3 is compositionally stable under elevated temperatures, the cubic perovskite α‐phase is thermodynamically stable only at >330°C and...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs: Marshall, AR, Sansom, HC, McCarthy, MM, Warby, JH, Ashton, OJ, Wenger, B, Snaith, HJ
Formaat: Journal article
Taal:English
Gepubliceerd in: Wiley 2020
_version_ 1826285401085575168
author Marshall, AR
Sansom, HC
McCarthy, MM
Warby, JH
Ashton, OJ
Wenger, B
Snaith, HJ
author_facet Marshall, AR
Sansom, HC
McCarthy, MM
Warby, JH
Ashton, OJ
Wenger, B
Snaith, HJ
author_sort Marshall, AR
collection OXFORD
description All‐inorganic perovskite materials are attractive alternatives to organic‐inorganic perovskites because of their potential for higher thermal stability. While CsPbI3 is compositionally stable under elevated temperatures, the cubic perovskite α‐phase is thermodynamically stable only at >330°C and the low‐temperature perovskite γ−phase is metastable and highly susceptible to non‐perovskite δ‐phase conversion in moisture. Many methods have been reported which show that incorporation of acid (aqueous HI) or “HPbI3” – recently shown to be dimethylammonium lead iodide (DMAPbI3) – lower the annealing temperature required to produce the black, perovskite phase of CsPbI3. The optical and crystallographic data presented here show that DMA can successfully incorporate as an A‐site cation to replace Cs in the CsPbI3 perovskite material. This describes the stabilization and lower phase transition temperature reported in the literature when HI or HPbI3 are used as precursors for CsPbI3. The Cs‐DMA alloy only forms a pure‐phase material up to ∽25% DMA; at higher concentrations the CsPbI3 and DMAPbI3 begin to phase segregate. These alloyed materials are more stable to moisture than neat CsPbI3, but do not represent a fully inorganic perovskite material.
first_indexed 2024-03-07T01:28:16Z
format Journal article
id oxford-uuid:92b560fb-dca0-4871-bf40-f5dfefbb2f30
institution University of Oxford
language English
last_indexed 2024-03-07T01:28:16Z
publishDate 2020
publisher Wiley
record_format dspace
spelling oxford-uuid:92b560fb-dca0-4871-bf40-f5dfefbb2f302022-03-26T23:27:30ZDimethylammonium: An A‐site Cation for Modifying CsPbI3Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:92b560fb-dca0-4871-bf40-f5dfefbb2f30EnglishSymplectic ElementsWiley2020Marshall, ARSansom, HCMcCarthy, MMWarby, JHAshton, OJWenger, BSnaith, HJAll‐inorganic perovskite materials are attractive alternatives to organic‐inorganic perovskites because of their potential for higher thermal stability. While CsPbI3 is compositionally stable under elevated temperatures, the cubic perovskite α‐phase is thermodynamically stable only at >330°C and the low‐temperature perovskite γ−phase is metastable and highly susceptible to non‐perovskite δ‐phase conversion in moisture. Many methods have been reported which show that incorporation of acid (aqueous HI) or “HPbI3” – recently shown to be dimethylammonium lead iodide (DMAPbI3) – lower the annealing temperature required to produce the black, perovskite phase of CsPbI3. The optical and crystallographic data presented here show that DMA can successfully incorporate as an A‐site cation to replace Cs in the CsPbI3 perovskite material. This describes the stabilization and lower phase transition temperature reported in the literature when HI or HPbI3 are used as precursors for CsPbI3. The Cs‐DMA alloy only forms a pure‐phase material up to ∽25% DMA; at higher concentrations the CsPbI3 and DMAPbI3 begin to phase segregate. These alloyed materials are more stable to moisture than neat CsPbI3, but do not represent a fully inorganic perovskite material.
spellingShingle Marshall, AR
Sansom, HC
McCarthy, MM
Warby, JH
Ashton, OJ
Wenger, B
Snaith, HJ
Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title_full Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title_fullStr Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title_full_unstemmed Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title_short Dimethylammonium: An A‐site Cation for Modifying CsPbI3
title_sort dimethylammonium an a site cation for modifying cspbi3
work_keys_str_mv AT marshallar dimethylammoniumanasitecationformodifyingcspbi3
AT sansomhc dimethylammoniumanasitecationformodifyingcspbi3
AT mccarthymm dimethylammoniumanasitecationformodifyingcspbi3
AT warbyjh dimethylammoniumanasitecationformodifyingcspbi3
AT ashtonoj dimethylammoniumanasitecationformodifyingcspbi3
AT wengerb dimethylammoniumanasitecationformodifyingcspbi3
AT snaithhj dimethylammoniumanasitecationformodifyingcspbi3