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Published on: March 19, 2017
Fused-Ring Electron Acceptors as a Versatile Additive Platform for Efficient Perovskite Photovoltaics
Yiting Jiang1, Huachao Zai1,2, Xiaojian Zheng1
1State Key Laboratory of Advanced Waterproof Materials, School of Materials Science and Engineering, Peking University, Beijing 100871, P. R. China.
Researchers developed a new additive design for perovskite solar cells (PSCs) using fused-ring electron acceptors (FREAs). This approach enhances reproducibility and device stability, achieving a 26.66% efficiency and maintaining performance over 2150 hours.
Area of Science:
- Materials Science
- Photovoltaics
- Organic Electronics
Background:
- Perovskite solar cells (PSCs) efficiency is often limited by defects and poor reproducibility.
- Existing additives for PSCs lack a reliable molecular design platform, hindering consistent performance across research groups.
Purpose of the Study:
- To introduce a general and rational additive design platform based on fused-ring electron acceptors (FREAs) for reproducible and efficient PSCs.
- To demonstrate the versatility and reliability of FREAs in modulating perovskite film properties for improved device performance and stability.
Main Methods:
- Utilized fused-ring electron acceptors (FREAs) as a molecular design platform for additive development.
- Tailored FREA main chains to modulate energy level alignment and facilitate charge transport.
- Designed FREA side chains to induce specific film morphology and suppress ion migration.
Main Results:
- Achieved a champion power conversion efficiency of 26.66% (26.35% certified) with an optimized FREA additive.
- Demonstrated significantly improved device stability, with less than 8% efficiency loss after 2150 hours of continuous operation under 1 sun illumination.
Conclusions:
- FREA-based additives offer a reproducible and versatile platform for designing high-performance and stable perovskite solar cells.
- Strategic molecular design of FREAs enables precise control over film properties, leading to enhanced charge transport and suppressed ion migration.
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