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Updated: Jan 18, 2026

Facile Synthesis of Colloidal Lead Halide Perovskite Nanoplatelets via Ligand-Assisted Reprecipitation
Published on: October 1, 2019
Differential Ligand-Cation Interactions Enable 2D-Template-Induced Ordered Assembly for Efficient Tin-Based
Yu Zou1, Jian Liu2, Yide Chang3
1Future Photovoltaics Research Center, Global Institute of Future Technology (GIFT), Shanghai Jiao Tong University, Shanghai, P. R. China.
Environmentally friendly tin halide perovskite (THP) solar cells utilize a fullerene derivative ligand for sequential crystallization. This strategy enhances film quality, boosting power conversion efficiency to 16.6% and device stability.
Area of Science:
- Materials Science
- Renewable Energy
- Photovoltaics
Background:
- Tin halide perovskites (THPs) are emerging as eco-friendly alternatives to lead-based solar cells.
- Improving THP film quality is crucial for high-performance devices, often achieved by templating the 3D phase with 2D components.
- Simultaneous crystallization of 2D and 3D phases hinders ordered growth and device performance.
Purpose of the Study:
- To develop a method for controlled sequential crystallization of 2D and 3D THP phases.
- To enhance the quality and stability of tin halide perovskite films for solar cell applications.
- To investigate the role of ligand-cation interactions in programming perovskite assembly.
Main Methods:
- Introduction of a fullerene derivative ligand to mediate distinct ligand-cation interactions.
- Programming A-site cation-mediated sequential assembly and crystallization of 2D and 3D THP phases.
- Fabrication and characterization of THP solar cells using the developed ligand strategy.
Main Results:
- Achieved sequential crystallization with the 2D phase templating the ordered epitaxial growth of the 3D phase.
- Produced highly crystalline, oriented THP films with a homogeneous 2D/3D heterojunction.
- Resulting devices demonstrated a champion power conversion efficiency of 16.6%.
- Unencapsulated devices showed a nine-fold increase in T90 lifetime (882 h vs. 99 h) under operational stress.
Conclusions:
- The fullerene derivative ligand effectively controls sequential crystallization, leading to superior THP film morphology.
- The developed method significantly enhances both the efficiency and operational stability of tin halide perovskite solar cells.
- This approach offers a promising pathway for the commercialization of stable and efficient THP photovoltaics.
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