Two-Dimensional Perovskite Quantum Dot Building Blocks toward Efficient 2D/3D Perovskite Heterostructures in Photovoltaics

钙钛矿(结构) 材料科学 量子点 光伏 异质结 能量转换效率 光电子学 纳米技术 光伏系统 扩散 钙钛矿太阳能电池 载流子寿命 量子效率 溶解过程 工作(物理) 载流子 相对湿度 电子迁移率
作者
Yunping Lang,Xinxuan Yang,Yang Shao,Lin Fan,Xiaoyan Liu,Nannan Yang,Huilian Liu,Fengyou Wang,Jinghai Yang,Lili Yang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:18 (13): 19015-19024
标识
DOI:10.1021/acsami.5c24915
摘要

Two-dimensional/three-dimensional (2D/3D) perovskite solar cells (PSCs) have attracted considerable attention due to their promising performance and environmental stability. However, conventional in situ grown 2D/3D perovskites form a layered structure with 2D organic spacer layers aligned parallel to the 3D perovskite, impeding out-of-plane carrier transport. Moreover, the distinct cation size between 2D and 3D perovskites triggers ion diffusion at the heterointerface, leading to the formation of a mixed-phase 2D perovskite and increased defect density, which severely limits device performance. To address these issues, we synthesized 2D perovskite quantum dots (QDs) modified with poly(3-hexylthiophene) (P3HT), acting as building blocks, which were subsequently deposited onto a 3D perovskite film to construct novel 2D QDs@P3HT/3D PSCs. This strategy effectively suppresses defect accumulation caused by mixed phases in traditional 2D/3D perovskite. Furthermore, this design facilitates additional vertical carrier transport pathways, alleviating the out-of-plane carrier transport limitation in conventional layered 2D/3D perovskite. As a result, the optimized devices achieve a power conversion efficiency of 25.04% and exhibit remarkable stability, retaining over 93% of their initial efficiency after 1200 h of aging under 85% relative humidity at 25 °C. This work offers a viable strategy to balance efficiency and stability in perovskite photovoltaics.
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