Quantification of Ion Migration in CH3NH3PbI3 Perovskite Solar Cells by Transient Capacitance Measurements
arXiv:1801.08519 · doi:10.1039/c9mh00445a
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 I- ions. We furthermore observe that the activation energy of mobile I- ions (0.29 eV) is highly reproducible for different devices, while the activation energy of mobile MA+ depends strongly on device fabrication. This quantification of mobile ions in MAPbI3 will lead to a better understanding of ion migration and its role in operation and degradation of perovskite solar cells.
References in corpus (4)
- What is moving in hybrid halide perovskite solar cells?
- Unravelling the role of vacancies in lead halide perovskite through electrical switching of photoluminescence
- Microseconds, milliseconds and seconds: deconvoluting the dynamic behaviour of planar perovskite solar cells
- The Sobering Reality of Perovskite/Si Tandem Solar Cells under Realistic Operating Conditions
Cited by in corpus (14)
- Shining Light on Photoluminescence Properties of Metal Halide Perovskites
- Probing the ionic defect landscape in halide perovskite solar cells
- Quantifying Charge Carrier Mobilities and Recombination Rates in Metal Halide Perovskites from Time-Resolved Microwave Photo-conductivity Measurements
- Quantifying mobile ions in perovskite-based devices with temperature-dependent capacitance measurements: frequency versus time domain
- Revealing the doping density in perovskite solar cells and its impact on device performance
- Modelling Grain Boundaries in Polycrystalline Halide Perovskite Solar Cells
- Tracing Ion Migration in Halide Perovskites with Machine Learned Force Fields
- Improved evaluation of deep-level transient spectroscopy on perovskite solar cells reveals ionic defect distribution
- Nanoparticulate Metal Oxide Top Electrode Interface Modification Improves the Thermal Stability of Inverted Perovskite Photovoltaics
- Substrate-dependent Photoconductivity Dynamics in a High-efficiency Hybrid Perovskite Alloy
- "Forbidden" polarisation and extraordinary piezoelectric effect in organometallic lead halide perovskites
- Ion Mobility Independent Large Signal Switching of Perovskite Devices
- Efficiency limits of Perovskite Solar Cells with Transition Metal Oxides as Hole Transport Layers
- Molecular Bond Engineering and Feature Learning for the Design of Hybrid Organic-Inorganic Perovskites Solar Cells with Strong Non-Covalent Halogen-Cation Interactions