Ling Xufeng, Zhu Hongwei, Xu Weidong, Liu Cheng, Pan Linfeng, Ren Dan, Yuan Jianyu, Larson Bryon W, Grätzel Carole, Kirmani Ahmad R, Ouellette Olivier, Krishna Anurag, Sun Jianguo, Zhang Chunyang, Li Youyong, Zakeeruddin Shaik M, Gao Jing, Liu Yuhang, Durrant James R, Luther Joseph M, Ma Wanli, Grätzel Michael
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory of Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu, 215123, China.
Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Station 6, 1015, Lausanne, Switzerland.
Angew Chem Int Ed Engl. 2021 Dec 20;60(52):27299-27306. doi: 10.1002/anie.202112555. Epub 2021 Nov 18.
α-Formamidinium lead iodide (α-FAPbI ) is one of the most promising candidate materials for high-efficiency and thermally stable perovskite solar cells (PSCs) owing to its outstanding optoelectrical properties and high thermal stability. However, achieving a stable form of α-FAPbI where both the composition and the phase are pure is very challenging. Herein, we report on a combined strategy of precursor engineering and grain anchoring to successfully prepare methylammonium (MA)-free and phase-pure stable α-FAPbI films. The incorporation of volatile FA-based additives in the precursor solutions completely suppresses the formation of non-perovskite δ-FAPbI during film crystallization. Grains of the desired α-phase are anchored together and stabilized when 4-tert-butylbenzylammonium iodide is permeated into the α-FAPbI film interior via grain boundaries. This cooperative scheme leads to a significantly increased efficiency close to 21 % for FAPbI perovskite solar cells. Moreover, the stabilized PSCs exhibit improved thermal stability and maintained ≈90 % of their initial efficiency after storage at 50 °C for over 1600 hours.
α-甲脒碘化铅(α-FAPbI₃)因其优异的光电性能和高热稳定性,是高效热稳定钙钛矿太阳能电池(PSC)最具潜力的候选材料之一。然而,要获得一种组成和相均纯净的稳定α-FAPbI₃形式极具挑战性。在此,我们报道了一种前驱体工程和晶粒锚固相结合的策略,成功制备出无甲胺(MA)且相纯的稳定α-FAPbI₃薄膜。在前驱体溶液中加入挥发性的基于FA的添加剂,在薄膜结晶过程中完全抑制了非钙钛矿δ-FAPbI₃的形成。当4-叔丁基苄基碘化铵通过晶界渗透到α-FAPbI₃薄膜内部时,所需α相的晶粒被锚固在一起并得以稳定。这种协同方案使FAPbI₃钙钛矿太阳能电池的效率显著提高,接近21%。此外,稳定后的PSC表现出更好的热稳定性,在50℃下储存超过1600小时后仍保持约90%的初始效率。