Quantification of Ion Migration in CH3NH3PbI3 Perovskite Solar Cells by Transient Capacitance Measurements
Moritz H. Futscher, Ju Min Lee, Lucie McGovern, Loreta A. Muscarella,, Tianyi Wang, Muhammad Irfan Haider, Azhar Fakharuddin, Lukas Schmidt-Mende, and Bruno Ehrler

TL;DR
This study quantifies ion migration in MAPbI3 perovskite solar cells using transient capacitance measurements, revealing ion species, their concentrations, diffusion coefficients, and activation energies to better understand device degradation.
Contribution
It provides the first detailed quantification of mobile ion species, their properties, and phase-dependent behavior in MAPbI3 perovskite solar cells, advancing understanding of ion migration effects.
Findings
Identified three migrating ion species, including iodide and methylammonium.
Mobile MA+ ions have higher concentration but lower diffusion coefficient than I- ions.
Activation energy for I- ions is consistent across devices, while MA+ activation energy varies with fabrication.
Abstract
Solar cells based on organic-inorganic metal halide perovskites show efficiencies close to highly-optimized silicon solar cells. However, ion migration in the perovskite films leads to device degradation and impedes large scale commercial applications. We use transient ion-drift measurements to quantify activation energy, diffusion coefficient, and concentration of mobile ions in methylammonium lead triiodide (MAPbI3) perovskite solar cells, and find that their properties change close to the tetragonal-to-orthorhombic phase transition temperature. We identify three migrating ion species which we attribute to the migration of iodide (I-) and methylammonium (MA+). We find that the concentration of mobile MA+ ions is one order of magnitude higher than the one of mobile I- ions, and that the diffusion coefficient of mobile MA+ ions is three orders of magnitude lower than the one for mobile…
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