High Power Irradiance Dependence of Charge Species Dynamics in Hybrid Perovskites and Kinetic Evidence for Transient Vibrational Stark Effect in Formamidinium

Rafal Rakowski, William Fisher, Joaquín Calbo, Muhamad Z. Mokhtar, Xinxing Liang, Dong Ding, Jarvist M. Frost, Saif A. Haque, Aron Walsh, Piers R.F. Barnes, Jenny Nelson, Jasper J. van Thor

Research output: Contribution to journalArticlepeer-review

Abstract

Hybrid halide perovskites materials have the potential for both photovoltaic and light-emitting devices. Relatively little has been reported on the kinetics of charge relaxation upon intense excitation. In order to evaluate the illumination power density dependence on the charge recombination mechanism, we have applied a femtosecond transient mid-IR absorption spectroscopy with strong excitation to directly measure the charge kinetics via electron absorption. The irradiance-dependent relaxation processes of the excited, photo-generated charge pairs were quantified in polycrystalline MAPbI3, MAPbBr3, and (FAPbI3)0.97 (MAPbBr3)0.03 thin films that contain either methylamonium (MA) or formamidinium (FA). This report identifies the laser-generated charge species and provides the kinetics of Auger, bimolecular and excitonic decay components. The inter-band electron-hole (bimolecular) recombination was found to dominate over Auger recombination at very high pump irradiances, up to the damage threshold. The kinetic analysis further provides direct evidence for the carrier field origin of the vibrational Stark effect in a formamidinium containing perovskite material. The results suggest that radiative excitonic and bimolecular recombination in MAPbI3 at high excitation densities could support light-emitting applications.

Original languageEnglish
Article number1616
JournalNanomaterials
Volume12
Issue number10
DOIs
Publication statusPublished - 2022 May 1

Bibliographical note

Funding Information:
Acknowledgments: We thank M. Sachs for assistance. We are grateful to the UK Materials and Molecular Modelling Hub for computational resources, which are partially funded by EPSRC (EP/P020194/1 and EP/T022213/1).

Funding Information:
Funding: This research was funded by the Engineering and Physical Sciences Research Council (EPSRC) via Award No. EP/R020574/1.

Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.

All Science Journal Classification (ASJC) codes

  • Chemical Engineering(all)
  • Materials Science(all)

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