Fundamental Research (Mar 2022)

Highly oriented MAPbI3 crystals for efficient hole-conductor-free printable mesoscopic perovskite solar cells

  • Shuang Liu,
  • Deyi Zhang,
  • Yusong Sheng,
  • Weihua Zhang,
  • Zhaotong Qin,
  • Minchao Qin,
  • Sheng Li,
  • Yifan Wang,
  • Chenxu Gao,
  • Qifei Wang,
  • Yue Ming,
  • Chao Liu,
  • Kai Yang,
  • Qingyi Huang,
  • Jianhang Qi,
  • Qiaojiao Gao,
  • Kai Chen,
  • Yue Hu,
  • Yaoguang Rong,
  • Xinhui Lu,
  • Anyi Mei,
  • Hongwei Han

Journal volume & issue
Vol. 2, no. 2
pp. 276 – 283

Abstract

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Highly crystalline perovskite films with large grains and few grain boundaries are conducive for efficient and stable perovskite solar cells. Current methods for preparing perovskite films are mostly based on a fast crystallization process, with rapid nucleation and insufficient growth. In this study, MAPbI3 perovskite with inhibited nucleation and promoted growth in the TiO2/ZrO2/carbon triple mesoscopic scaffold was crystallized by modulating the precursor and the crystallization process. N-methylformamide showed high solubility for both methylammonium iodide and PbI2 and hampered the formation of large colloids in the MAPbI3 precursor solution. Furthermore, methylammonium chloride was added to reduce large colloids, which are a possible source of nucleation sites. During the crystallization of MAPbI3, the solvent was removed at a slow controlled speed, to avoid rapid nucleation and provide sufficient time for crystal growth. As a result, highly oriented MAPbI3 crystals with suppressed non-radiative recombination and promoted charge transport were obtained in the triple mesoscopic layer with disordered pores. The corresponding hole-conductor-free, printable mesoscopic perovskite solar cells exhibited a highest power conversion efficiency of 18.82%. The device also exhibited promising long-term operational stability of 1000 h under continuous illumination at maximum power point at 55 ± 5 °C and damp-heat stability of 1340 h aging at 85 °C as well as 85% relative humidity.

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