@article{8506,
  author = {N. X. Li and S. X. Tao and Y. Chen and X. X. Niu and C. K. Onwudinanti and C. Hu and Z. W. Qiu and Z. Xu and G. Zheng and L. G. Wang and Y. Zhang and L. Li and H. Liu and Y. Z. Lun and J. W. Hong and X. Y. Wang and Y. Q. Liu and H. P. Xie and Y. L. Gao and Y. Bai and S. H. Yang and G. Brocks and Q. Chen and H. P. Zhou},
  title = {Cation and anion immobilization through chemical bonding enhancement with fluorides for stable halide perovskite solar cells},
  abstract = {Defects play an important role in the degradation processes of hybrid halide perovskite absorbers, impeding their application for solar cells. Among all defects, halide anion and organic cation vacancies are ubiquitous, promoting ion diffusion and leading to thin-film decomposition at surfaces and grain boundaries. Here, we employ fluoride to simultaneously passivate both anion and cation vacancies, by taking advantage of the extremely high electronegativity of fluoride. We obtain a power conversion efficiency of 21.46% (and a certified 21.3%-efficient cell) in a device based on the caesium, methylammonium (MA) and formamidinium (FA) triple-cation perovskite (Cs0.05FA0.54MA0.41)Pb(I0.98Br0.02)3 treated with sodium fluoride. The device retains 90% of its original power conversion efficiency after 1,000?h of operation at the maximum power point. With the help of first-principles density functional theory calculations, we argue that the fluoride ions suppress the formation of halide anion and organic cation vacancies, through a unique strengthening of the chemical bonds with the surrounding lead and organic cations.},
  year = {2019},
  journal = {Nature Energy},
  volume = {4},
  pages = {408-415},
  month = {5/2019},
  doi = {10.1038/s41560-019-0382-6},
  language = {eng},
}