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构建软钙钛矿-衬底界面以动态调制倒置太阳能电池中钙钛矿薄膜的光稳定性,光照超过6200小时。

Constructing Soft Perovskite-Substrate Interfaces for Dynamic Modulation of Perovskite Film in Inverted Solar Cells with Over 6200 Hours Photostability.

作者信息

Lv Wenxuan, Hu Zhaoying, Qiu Wei, Yan Dongdong, Li Meicheng, Mei Anyi, Xu Ligang, Chen Runfeng

机构信息

Key Laboratory for Organic Electronics and Information Displays (KLOEID) & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, 9 Wenyuan Road, Nanjing, 210023, China.

State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, School of New Energy, North China Electric Power University, Beijing, 100192, China.

出版信息

Adv Sci (Weinh). 2022 Oct;9(28):e2202028. doi: 10.1002/advs.202202028. Epub 2022 Aug 17.

Abstract

High-performance perovskite solar cells (PSCs) depend heavily on the quality of perovskite films, which is closely related to the lattice distortion, perovskite crystallization, and interfacial defects when being spin-coated and annealed on the substrate surface. Here, a dynamic strategy to modulate the perovskite film formation by using a soft perovskite-substrate interface constructed by employing amphiphilic soft molecules (ASMs) with long alkyl chains and Lewis base groups is proposed. The hydrophobic alkyl chains of ASMs interacted with poly(triarylamine) (PTAA) greatly improve the wettability of PTAA to facilitate the nucleation and growth of perovskite crystals, while the Lewis base groups bound to perovskite lattices significantly passivate the defects in situ. More importantly, this soft perovskite-substrate interface with ASMs between PTAA and perovskite film can dynamically match the lattice distortion with reduced interfacial residual strain upon perovskite crystallization and thermal annealing owing to the soft self-adaptive long-chains, leading to high-quality perovskite films. Thus, the inverted PSCs show a power conversion efficiency approaching 20% with good reproducibility and negligible hysteresis. More impressively, the unencapsulated device exhibits state-of-the-art photostability, retaining 84% of its initial efficiency under continuous simulated 1-sun illumination for more than 6200 h at elevated temperature (≈65 °C).

摘要

高性能钙钛矿太阳能电池(PSC)在很大程度上依赖于钙钛矿薄膜的质量,而钙钛矿薄膜的质量与在衬底表面旋涂和退火时的晶格畸变、钙钛矿结晶以及界面缺陷密切相关。在此,我们提出了一种动态策略,通过使用由具有长烷基链和路易斯碱基团的两亲性软分子(ASM)构建的柔软钙钛矿-衬底界面来调控钙钛矿薄膜的形成。ASM的疏水烷基链与聚(三芳基胺)(PTAA)相互作用极大地改善了PTAA的润湿性,以促进钙钛矿晶体的成核和生长,而与钙钛矿晶格结合的路易斯碱基团则显著原位钝化缺陷。更重要的是,由于柔软的自适应长链,PTAA和钙钛矿薄膜之间具有ASM的这种柔软钙钛矿-衬底界面在钙钛矿结晶和热退火时能够动态匹配晶格畸变并降低界面残余应变,从而得到高质量的钙钛矿薄膜。因此,倒置PSC的功率转换效率接近20%,具有良好的重现性和可忽略不计的滞后现象。更令人印象深刻的是,未封装的器件表现出最先进的光稳定性,在高温(≈65°C)下连续模拟1太阳光照超过6200小时后仍保留其初始效率的84%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed8/9534936/da18ab50a220/ADVS-9-2202028-g003.jpg

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