Related Experiment Video
Updated: Jun 13, 2025

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Cation and Octahedral Synergistic Regulation for Stable FAPbI3 Perovskite Solar Cells
Guangcai Hu1, Ziyue Zhao2, Yang Shen2
1State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering, and Hangzhou Global Scientific and Technological Innovation Center, Zhejiang University, Hangzhou, Zhejiang, 310027, P. R. China.
Abstract:
Formamidinium lead iodide (FAPbI3) perovskite, one of the most promising light-absorbing materials, faces substantial stability issues, including FA+ organic component volatilization and undesirable phase transition between corner-sharing and face-sharing [PbI6]4 ̶ octahedra. Especially, the asymmetric hydrogen bonding, arising from oriented and irregularly spinning FA+ cation, accelerates these transformations, compromising both the efficiency and long-term stability of FAPbI3 PSCs. Herein, a robust strategy is reported to stabilize FAPbI3 perovskite by using tricyclohexylphosphine trifluoromethanesulfonate (Cy3PH+SO3CF3 -) to strengthen hydrogen bonds within FA+ and alleviate octahedral deformation. The hydrogen-bonding capacity of Cy3PH+ effectively constrains and stabilizes orientated FA+ through strong hydrogen bonds (F─H, N─H), while the strong electronegative SO3CF3 - ion modifies [PbI6]4 - octahedral deformation by diversified covalent bonds (Pb─F, Pb─O) and releases the internal stress of the lattice. As such, the resulting FAPbI3 demonstrates mitigated organic volatilization and suppressed phase transition, significantly enhancing phase stability under thermal/humidity stress conditions. Moreover, because of co-regulated FA+ cation and octahedral lattice, FAPbI3 perovskite exhibits improved carrier dynamics and better matched energy-level alignment with carrier transport layers. The optimized FAPbI3-based PSCs deliver an impressive efficiency of 25.93% and exhibit exceptional stability, retaining 97% of initial efficiency after over 1500 h maximum power point tracking.
Related Concept Videos
Valence Bond Theory
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...

