TY - JOUR
T1 - Guanidinium Substitution Improves Self-Healing and Photodamage Resilience of MAPbI3
AU - Singh, Pallavi
AU - Ceratti, Davide Raffaele
AU - Soffer, Yahel
AU - Bera, Sudipta
AU - Feldman, Yishay
AU - Elbaum, Michael
AU - Oron, Dan
AU - Cahen, David
AU - Hodes, Gary
N1 - Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society.
PY - 2024/11/28
Y1 - 2024/11/28
N2 - Self-healing materials can become game changers for developing sustainable (opto)electronics. APbX3 halide (=X-) perovskites, HaPs, have shown a remarkable ability to self-heal damage. While we demonstrated self-healing in pure HaP compounds, in single crystals, and in polycrystalline thin films (as used in most devices), HaP compositions with multiple A+ (and X-) constituents are preferred for solar cells. We now show self-healing in mixed A+ HaPs. Specifically, if at least 15 atom % of the methylammonium (MA+) A cation is substituted for by guanidinium (Gua+) or acetamidinium (AA+), then the self-healing rate after damage is enhanced. In contrast, replacing MA+ with dimethylammonium (DMA+), comparable in size to Gua+ or AA+, does not alter this rate. Based on the times for self-healing, we infer that the rate-determining step involves short-range diffusion of A+ and/or Pb2+ cations and that the self-healing rate correlates with the strain in the material, the A+ cation dipole moment, and H-bonding between A+ and I-. These insights may offer clues for developing a detailed self-healing mechanism and understanding the kinetics to guide the design of self-healing materials. Fast recovery kinetics are important from the device perspective, as they allow complete recovery in devices during operation or when switched off (LEDs)/in the dark (photovoltaics).
AB - Self-healing materials can become game changers for developing sustainable (opto)electronics. APbX3 halide (=X-) perovskites, HaPs, have shown a remarkable ability to self-heal damage. While we demonstrated self-healing in pure HaP compounds, in single crystals, and in polycrystalline thin films (as used in most devices), HaP compositions with multiple A+ (and X-) constituents are preferred for solar cells. We now show self-healing in mixed A+ HaPs. Specifically, if at least 15 atom % of the methylammonium (MA+) A cation is substituted for by guanidinium (Gua+) or acetamidinium (AA+), then the self-healing rate after damage is enhanced. In contrast, replacing MA+ with dimethylammonium (DMA+), comparable in size to Gua+ or AA+, does not alter this rate. Based on the times for self-healing, we infer that the rate-determining step involves short-range diffusion of A+ and/or Pb2+ cations and that the self-healing rate correlates with the strain in the material, the A+ cation dipole moment, and H-bonding between A+ and I-. These insights may offer clues for developing a detailed self-healing mechanism and understanding the kinetics to guide the design of self-healing materials. Fast recovery kinetics are important from the device perspective, as they allow complete recovery in devices during operation or when switched off (LEDs)/in the dark (photovoltaics).
UR - http://www.scopus.com/inward/record.url?scp=85209709152&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.4c06090
DO - 10.1021/acs.jpcc.4c06090
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 39634028
AN - SCOPUS:85209709152
SN - 1932-7447
VL - 128
SP - 19999
EP - 20008
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 47
ER -