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Abstract
The bidirectional migration of halides and silver causes irreversible chemical corrosion to the electrodes and perovskite layer, affecting long-term operation stability of perovskite solar cells. Here we propose a silver coordination-induced n-doping of [6,6]-phenyl-C61-butyric acid methyl ester strategy to safeguard Ag electrode against corrosion and impede the migration of iodine within the PSCs. Meanwhile, the coordination between DCBP and silver induces n-doping in the PCBM layer, accelerating electron extraction from the perovskite layer. The resultant PSCs demonstrate an efficiency of 26.03% (certified 25.51%) with a minimal non-radiative voltage loss of 126 mV. The PCE of resulting devices retain 95% of their initial value after 2500 h of continuous maximum power point tracking under one-sun irradiation, and > 90% of their initial value even after 1500 h of accelerated aging at 85 °C and 85% relative humidity.
The bidirectional halide and silver migration cause irreversible chemical corrosion to electrodes and perovskite layer. Here, the authors employ 4,4’-dicyano-2,2’-bipyridine in the electron transport layer to coordinate silver and iodide, realizing stable solar cells with efficiency over 26%.
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1 Chongqing University, Key Laboratory of Optoelectronic Technology & Systems (Ministry of Education), Chongqing, China (GRID:grid.190737.b) (ISNI:0000 0001 0154 0904)
2 Huazhong University of Science and Technology, Wuhan National Laboratory for Optoelectronics, Wuhan, China (GRID:grid.33199.31) (ISNI:0000 0004 0368 7223)
3 Chongqing University, Key Laboratory of Optoelectronic Technology & Systems (Ministry of Education), Chongqing, China (GRID:grid.190737.b) (ISNI:0000 0001 0154 0904); Yanshan University, College of Information Science and Engineering, Qinhuangdao, China (GRID:grid.413012.5) (ISNI:0000 0000 8954 0417)