TY - JOUR
T1 - Multitechnique Detection of Lead Iodide Hybrid Perovskite Degradation Pathways under Varying Electric Fields
AU - Nguyen, Linh Lan
AU - Zhang, Qiannan
AU - Bradley, David G.
AU - Xing, Zengshan
AU - Salim, Teddy
AU - Li, Patrick Wen Feng
AU - Mishra, Pritish
AU - Mueller, Aaron
AU - Mondal, Shreyan
AU - Chong, Ka Shing
AU - Sum, Tze Chien
AU - Hanna, John V.
AU - Duchamp, Martial
AU - Lam, Yeng Ming
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025
Y1 - 2025
N2 - Although hybrid perovskite-based devices have made significant advances in terms of device performance, long-term stability remains a major challenge to widespread implementation. A unified understanding of the complexity describing the degradation of these types of materials is absent, and in this work, one common hybrid perovskite material, methylammonium lead iodide (MAPI), is used as a vehicle to show how a unified understanding can be achieved using complementary characterization techniques. This work uses low-dose in situ electron microscopes with electric fields ranging from 2.5 to 5 V/μm in a scanning electron microscope before focusing on the lower fields of 1.25 and 2.5 V/μm, where an electric threshold is identified. The results demonstrate that material loss is initiated at the MAPI grain boundaries near the negative electrode interface, where MA+ is reduced. Above the electrochemical threshold, extensive material volatilization and amorphous layer formation were detected, accompanied by significant PL quenching. High-field solid-state MAS NMR and materials modeling indicate that the MAPI decomposition process is a simultaneous combination of iodine migration, vacancy formation, and organic cation decomposition. The 1H MAS NMR data from the as-synthesized MAPI show direct evidence of preexisting iodine vacancies that induce the formation of CH3NH2, forming possible dative coordination to the lead framework positions. Subsequent data from MAPI degraded under exposure to electric fields (1.25 and 2.50 V/μm) directly demonstrate the presence of decomposition products such as NH4I, CH3I, and CH2I2 through pinhole formation at the electrochemical threshold and more widespread damage induced above this threshold. The methodology presented here can be applied to investigate other hybrid perovskite materials through direct spin coating on the corresponding substrates, deepening our understanding and providing insights for improved device stability.
AB - Although hybrid perovskite-based devices have made significant advances in terms of device performance, long-term stability remains a major challenge to widespread implementation. A unified understanding of the complexity describing the degradation of these types of materials is absent, and in this work, one common hybrid perovskite material, methylammonium lead iodide (MAPI), is used as a vehicle to show how a unified understanding can be achieved using complementary characterization techniques. This work uses low-dose in situ electron microscopes with electric fields ranging from 2.5 to 5 V/μm in a scanning electron microscope before focusing on the lower fields of 1.25 and 2.5 V/μm, where an electric threshold is identified. The results demonstrate that material loss is initiated at the MAPI grain boundaries near the negative electrode interface, where MA+ is reduced. Above the electrochemical threshold, extensive material volatilization and amorphous layer formation were detected, accompanied by significant PL quenching. High-field solid-state MAS NMR and materials modeling indicate that the MAPI decomposition process is a simultaneous combination of iodine migration, vacancy formation, and organic cation decomposition. The 1H MAS NMR data from the as-synthesized MAPI show direct evidence of preexisting iodine vacancies that induce the formation of CH3NH2, forming possible dative coordination to the lead framework positions. Subsequent data from MAPI degraded under exposure to electric fields (1.25 and 2.50 V/μm) directly demonstrate the presence of decomposition products such as NH4I, CH3I, and CH2I2 through pinhole formation at the electrochemical threshold and more widespread damage induced above this threshold. The methodology presented here can be applied to investigate other hybrid perovskite materials through direct spin coating on the corresponding substrates, deepening our understanding and providing insights for improved device stability.
KW - degradation
KW - halide perovskite
KW - in situ photoluminescence
KW - in situ transmission electron microscopy
KW - nuclear magnetic resonance
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U2 - 10.1021/acsnano.4c10370
DO - 10.1021/acsnano.4c10370
M3 - Article
AN - SCOPUS:105007904474
SN - 1936-0851
JO - ACS Nano
JF - ACS Nano
ER -