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Updated: Nov 2, 2025

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Electron-enriched thione enables strong Pb-S interaction for stabilizing high quality CsPbI3 perovskite films with
Xiaojia Xu1, Hao Zhang1, Erpeng Li1
1Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Shanghai Key Laboratory of Functional Materials Chemistry, Institute of Fine Chemicals, School of Chemistry and Molecular Engineering, East China University of Science and Technology Shanghai 200237 China wu.yongzhen@ecust.edu.cn.
Abstract:
Cesium lead iodide (CsPbI3) perovskite is a promising photovoltaic material with a suitable bandgap and high thermal stability. However, it involves complicated phase transitions, and black-phase CsPbI3 is mostly formed and stabilized at high temperatures (200-360 °C), making its practical application challenging. Here, for the first time, we have demonstrated a feasible route for growing high quality black-phase CsPbI3 thin films under mild conditions by using a neutral molecular additive of 4(1H)-pyridinethione (4-PT). The resulting CsPbI3 thin films are morphologically uniform and phase stable under ambient conditions, consisting of micron-sized grains with oriented crystal stacking. With a range of characterization experiments on intermolecular interactions, the electron-enriched thione group in 4-PT is distinguished to be critical to enabling a strong Pb-S interaction, which not only influences the crystallization paths, but also stabilizes the black-phase CsPbI3 via crystal surface functionalization. The 4-PT based CsPbI3 achieves 13.88% power conversion efficiency in a p-i-n structured device architecture, and encapsulated devices can retain over 85% of their initial efficiencies after 20 days of storage in an ambient environment, which are the best results among fully low-temperature processed CsPbI3 photovoltaics.

