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On the equilibrium electrostatic potential and light-induced charge redistribution in halide perovskite structures

  • Davide Regaldo
  • , Aleksandra Bojar
  • , Sean P. Dunfield
  • , Pilar Lopez-Varo
  • , Mathieu Frégnaux
  • , Vincent Dufoulon
  • , Shan Ting Zhang
  • , José Alvarez
  • , Joseph J. Berry
  • , Jean Baptiste Puel
  • , Philip Schulz
  • , Jean Paul Kleider
  • Université Paris-Saclay
  • Institut Photovoltaïque d'Ile-de-France
  • Sorbonne Université
  • National Renewable Energy Laboratory
  • University of Colorado
  • Université Versailles-Saint Quentin
  • Lamsid/EDF/R and D

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

Résumé

Lead halide perovskites are semiconductor materials which are employed as nonintentionally doped absorbers inserted between two selective carrier transport layers (SCTL), realizing a p-i-n or n-i-p heterojunction. In our study, we have developed and investigated a lateral device, based on methylammonium lead iodide (MAPbI3) in which the p-i-n heterojunction develops in the horizontal direction. Our research suggests that the effective doping level in the MAPbI3 film should be very low, below 1012 cm−3. Along the vertical direction, this doping level is not enough to screen the electric field of the buried heterojunction with the SCTL. The perovskite work function is therefore affected by the work function of the SCTL underneath. From drift-diffusion simulations, we show that intrinsic perovskite-SCTL structures develop mV range surface photovoltages (SPVs) under continuous illumination. However, perovskite-SCTL structures can develop SPVs of hundreds of mV, as confirmed by our measurements. We therefore analyzed the compatibility between low doping and low defect densities in the perovskite layer and such high SPV values using numerical modeling. It is shown that these high SPV values could originate from electronic processes due to large band offsets in the buried perovskite-SCTL heterojunctions, or at the SCTL-transparent conductive oxide (TCO) buried heterojunction. However, such electronic processes can hardly explain the long SPV persistence after switching off the illumination.

langue originaleAnglais
Pages (de - à)994-1002
Nombre de pages9
journalProgress in Photovoltaics: Research and Applications
Volume30
Numéro de publication8
Les DOIs
étatPublié - 1 août 2022

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