4.8 Article

Consistent Device Simulation Model Describing Perovskite Solar Cells in Steady-State, Transient, and Frequency Domain

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 26, Pages 23320-23328

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b04991

Keywords

perovskite solar cells; hysteresis; mobile ions; traps; impedance spectroscopy; IMPS; transient photo-current; drift-diffusion modeling

Funding

  1. Swiss Commission for Technology and Innovation [PEROLEC 18468.1 PFNM-NM]
  2. Swiss Federal Office of Energy (SFOE) [SI/501417-01]
  3. Swiss National Science Foundation (SNSF) [PV2050, 153952]
  4. European Union [760949]
  5. Fundacao de Amparo a Pesquisa do Estado de sao Paulo (Fapesp) [2018/05152-7]

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A variety of experiments on vacuum-deposited methylammonium lead iodide perovskite solar cells are presented, including JV curves with different scan rates, light intensity-dependent open-circuit voltage, impedance spectra, intensity-modulated photocurrent spectra, transient photocurrents, and transient voltage step responses. All these experimental data sets are successfully reproduced by a charge drift-diffusion simulation model incorporating mobile ions and charge traps using a single set of parameters. While previous modeling studies focused on a single experimental technique, we combine steady-state, transient, and frequency-domain simulations and measurements. Our study is an important step toward quantitative simulation of perovskite solar cells, leading to a deeper understanding of the physical effects in these materials. The analysis of the transient current upon voltage turn-on in the dark reveals that the charge injection properties of the interfaces are triggered by the accumulation of mobile ionic defects. We show that the current rise of voltage step experiments allow for conclusions about the recombination at the interface. Whether one or two mobile ionic species are used in the model has only a minor influence on the observed effects. A delayed current rise observed upon reversing the bias from +3 to -3 V in the dark cannot be reproduced yet by our drift-diffusion model. We speculate that a reversible chemical reaction of mobile ions with the contact material may be the cause of this effect, thus requiring a future model extension. A parameter variation is performed in order to understand the performance-limiting factors of the device under investigation.

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