Interplay between Ion Transport, Applied Bias, and Degradation under Illumination in Hybrid Perovskite p-i-n Devices
Author(s) -
Emily C. Smith,
Christie L. C. Ellis,
Hamza Javaid,
Lawrence A. Renna,
Yao Liu,
Thomas P. Russell,
Monojit Bag,
D. Venkataraman
Publication year - 2018
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.8b01121
Subject(s) - ion , capacitive sensing , materials science , capacitance , resistive touchscreen , dielectric spectroscopy , optoelectronics , ion transporter , diffusion , analytical chemistry (journal) , perovskite (structure) , ionic bonding , chemical physics , chemistry , electrochemistry , electrode , electrical engineering , physics , crystallography , organic chemistry , chromatography , thermodynamics , engineering
We studied ion transport in hybrid organic–inorganic perovskite p-i-n devices as a function of applied bias under device operating conditions. Using electrochemical impedance spectroscopy (EIS) and equivalent circuit modeling, we elucidated various resistive and capacitive elements in the device. We show that ion migration is predictably influenced by a low applied forward bias, characterized by an increased capacitance at the hole-transporting (HTM) and electron-transporting material (ETM) interfaces, as well as in bulk. However, unlike observations in n-i-p devices, we found that there is a capacitive discharge leading to ion redistribution in the bulk at high forward biases. Furthermore, we show that a chemical double-layer capacitance buildup as a result of ion accumulation impacts the electronic properties of the device, likely by inducing either charge pinning or charge screening, depending on the direction of the ion-induced field. Lastly, we extrapolate ion diffusion coefficients (∼10–7 cm2 s–1) a...
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