Effect of High Dipole Moment Cation on Layered 2D Organic–Inorganic Halide Perovskite Solar Cells

Shunquan Tan, Ning Zhou, Yihua Chen, Liang Li, Guilin Liu, Pengfei Liu, Cheng Zhu, Jiuzhou Lu, Wentao Sun, Qi Chen, Huanping Zhou*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

131 Citations (Scopus)

Abstract

Layered 2D organic–inorganic hybrid perovskite is appearing as a rising star in the photovoltaic field, thanks to its superior moisture resistance by the organic spacer cations. Unfortunately, these cations lead to high exciton binding energy in the 2D perovskites, which suffers from lower efficiency in the devices. It thus requires a clear criterion to select/design appropriate organic spacer cations to improve the device efficiency based on this class of materials. Here, 2,2,2-trifluoroethylamine (F3EA+) is introduced to combine with butylammonium (BA+) cations as mixed spacers. While BA+ enables self-assembly of 2D perovskite crystals by van der Waals interaction, the introduction of F3EA+ spacers with a high dipole moment suppress nonradiative recombination and promote separation of photogenerated electron–hole pairs by taking the advantage of electronegativity of fluorine. The resultant solar cells based on [(BA)1– x(F3EA)x]2(MA)3Pb4I13 exhibit substantially increased open circuit voltage and fill factor compared with that of (BA)2(MA)3Pb4I13. The champion [(BA)0.94(F3EA)0.06]2(MA)3Pb4I13 solar cell yields a power conversion efficiency of 12.51%, which is among the best performances so far. These findings suggest an effective strategy to design organic spacer cations in layered perovskite for solar cells and other optoelectronic applications.

Original languageEnglish
Article number1803024
JournalAdvanced Energy Materials
Volume9
Issue number5
DOIs
Publication statusPublished - 1 Feb 2019

Keywords

  • charge generation
  • charge recombination
  • exciton binding energy
  • high dipole moment
  • layered 2D perovskites

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