4.6 Article

Cation exchange for thin film lead iodide perovskite interconversion

Journal

MATERIALS HORIZONS
Volume 3, Issue 1, Pages 63-71

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5mh00170f

Keywords

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Funding

  1. EPSRC
  2. European Union Seventh Framework Programme [FP7] of the MESO project [604032]
  3. Oxford Photovoltaics Ltd through a Nanotechnology KTN CASE award
  4. Zuhlke Engineering AG
  5. EPSRC [EP/M024881/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/M024881/1] Funding Source: researchfish

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We report a new technique for tuning the bandgap of hybrid organic-inorganic halide perovskite materials. By dipping films of methylammonium or formamidinium lead triiodide (MAPbI(3) or FAPbI(3)) in solutions of formamidinium or methylammonium iodide (FAI or MAI) at room temperature, we are able to inter-convert through cation exchange between perovskite materials, allowing us to carefully tune the bandgap between 1.57 and 1.48 eV. We observe uniform conversion through the entirety of the bulk film, with no evidence for a bi-layered'' or graded structure. By applying this technique to solar cell devices, we are able to enhance the performance of the single cation devices. Furthermore, we demonstrate that this technique allows us to form pure black phase FAPbI(3) infiltrated into mesoporous scaffolds; this is normally infeasible since the pores confine the FAPbI(3) in a yellow non-perovskite phase with a much wider bandgap, which is not of practical use in solar cells or other optoelectronic devices. Additionally, this work provides evidence for molecular cation mobility in the halide perovskites, indicating that the cations play a role in ionic conduction as well as the mobile anions.

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