Accelerated Redox Reactions Enable Stable Tin‐Lead Mixed Perovskite Solar Cells
Dongxu He, Peng Chen, Mengmeng Hao, Miaoqiang Lyu, Zhiliang Wang, Shanshan Ding, Tongen Lin, Chengxi Zhang, Xin Wu, Evan G. Moore, Julian A. Steele, Ebinazar B. Namdas, Yang Bai, Lianzhou Wang
Abstract
Abstract The facile oxidation of Sn 2+ to Sn 4+ poses an inherent challenge that limits the efficiency and stability of tin‐lead mixed (Sn−Pb) perovskite solar cells (PSCs) and all‐perovskite tandem devices. In this work, we discover the sustainable redox reactions enabling self‐healing Sn−Pb perovskites, where their intractable oxidation degradation can be recovered to their original state under light soaking. Quantitative and operando spectroscopies are used to investigate the redox chemistry, revealing that metallic Pb 0 from the photolysis of perovskite reacts with Sn 4+ to regenerate Pb 2+ and Sn 2+ spontaneously. Given the sluggish redox reaction kinetics, V 3+ /V 2+ ionic pair is designed as an effective redox shuttle to accelerate the recovery of Sn−Pb perovskites from oxidation. The target Sn−Pb PSCs enabled by V 3+ /V 2+ ionic pair deliver an improved power conversion efficiency (PCE) of 21.22 % and excellent device lifespan, retaining nearly 90 % of its initial PCE after maximum power point tracking under light for 1,000 hours.