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通过氢键聚合物网络对 FA 基钙钛矿进行定向结晶,用于高效稳定的太阳能电池。

Orientated crystallization of FA-based perovskite via hydrogen-bonded polymer network for efficient and stable solar cells.

机构信息

Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), Nanjing, Jiangsu, 211816, P. R. China.

Shanghai Synchrotron Radiation Facility (SSRF), Shanghai Advanced Research Institute, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 239 Zhangheng Road, Shanghai, 201204, P. R. China.

出版信息

Nat Commun. 2023 Feb 2;14(1):573. doi: 10.1038/s41467-023-36224-6.

Abstract

Incorporating mixed ion is a frequently used strategy to stabilize black-phase formamidinum lead iodide perovskite for high-efficiency solar cells. However, these devices commonly suffer from photoinduced phase segregation and humidity instability. Herein, we find that the underlying reason is that the mixed halide perovskites generally fail to grow into homogenous and high-crystalline film, due to the multiple pathways of crystal nucleation originating from various intermediate phases in the film-forming process. Therefore, we design a multifunctional fluorinated additive, which restrains the complicated intermediate phases and promotes orientated crystallization of α-phase of perovskite. Furthermore, the additives in-situ polymerize during the perovskite film formation and form a hydrogen-bonded network to stabilize α-phase. Remarkably, the polymerized additives endow a strongly hydrophobic effect to the bare perovskite film against liquid water for 5 min. The unencapsulated devices achieve 24.10% efficiency and maintain >95% of the initial efficiency for 1000 h under continuous sunlight soaking and for 2000 h at air ambient of ~50% humid, respectively.

摘要

引入混合离子是一种常用的策略,可以稳定黑相甲脒碘化铅钙钛矿,以获得高效的太阳能电池。然而,这些器件通常会遭受光诱导的相分离和湿度不稳定性的影响。在此,我们发现,其根本原因是混合卤化物钙钛矿通常无法生长成均匀且高结晶的薄膜,这是由于在成膜过程中多种中间相导致的多个成核途径所致。因此,我们设计了一种多功能氟化添加剂,它可以抑制复杂的中间相,并促进钙钛矿α相的取向结晶。此外,添加剂在钙钛矿薄膜形成过程中原位聚合,并形成氢键网络以稳定α相。值得注意的是,聚合的添加剂赋予了裸钙钛矿薄膜强烈的疏水性,使其能够抵抗 5 分钟的液态水。未封装的器件在持续的阳光照射下实现了 24.10%的效率,并在连续 1000 小时和在约 50%湿度的空气环境中 2000 小时后,仍能保持初始效率的>95%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4821/9895431/25d3d6e415bd/41467_2023_36224_Fig1_HTML.jpg

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