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用于倒置钙钛矿太阳能电池的高度取向且有序的共组装单层膜

Highly Oriented and Ordered Co-Assembly Monolayers for Inverted Perovskite Solar Cells.

作者信息

Chang Yilin, Liu Le, Qi Lu, Du Jiajia, Du Qinglin, Yu Zhibin, Ma Zhiwei, Jiu Tonggang, Li Yuliang

机构信息

Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Qingdao, 266237, P. R. China.

Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2025 Jan 27;64(5):e202418883. doi: 10.1002/anie.202418883. Epub 2024 Dec 19.

Abstract

Perovskite solar cells with inverted architecture have remarkable power conversion efficiency (PCE) and operating stability based on self-assembled molecules (SAMs) hole transport layer. Homogeneous distribution and covalent binding mode of SAM monolayers are critical to improving interfacial property and reducing interfacial losses, which can be achieved through molecular design and co-assembly strategy. Here, we propose co-assembly strategy with SAM by employing a novel 2D π-conjugated structure graphdiyne derivative (PAG) with phosphoric acid groups. Through the π-π interaction and hydrogen bonding between PAG and SAM, the enhanced tridentate anchoring and highly ordered molecular orientation perpendicular to the substrate are successfully achieved. The improvement of interfacial characteristics further optimizes the crystalline quality and buried interface properties of perovskite films, allowing us to achieve a remarkable PCE of 26.10 % under standard illumination.

摘要

具有倒置结构的钙钛矿太阳能电池基于自组装分子(SAMs)空穴传输层具有卓越的功率转换效率(PCE)和运行稳定性。SAM单分子层的均匀分布和共价结合模式对于改善界面性质和减少界面损失至关重要,这可以通过分子设计和共组装策略来实现。在此,我们通过使用具有磷酸基团的新型二维π共轭结构石墨二炔衍生物(PAG),提出了与SAM的共组装策略。通过PAG与SAM之间的π-π相互作用和氢键,成功实现了增强的三齿锚定和垂直于基底的高度有序分子取向。界面特性的改善进一步优化了钙钛矿薄膜的晶体质量和掩埋界面性质,使我们在标准光照下实现了26.10%的卓越PCE。

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