Gong Cheng, Li Haiyun, Wang Huaxin, Zhang Cong, Zhuang Qixin, Wang Awen, Xu Zhiyuan, Cai Wensi, Li Ru, Li Xiong, Zang Zhigang
Key Laboratory of Optoelectronic Technology & Systems (Ministry of Education), Chongqing University, Chongqing, 400044, China.
Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, 430074, Hubei, China.
Nat Commun. 2024 Jun 10;15(1):4922. doi: 10.1038/s41467-024-49395-7.
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-C-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.
卤化物和银的双向迁移会对电极和钙钛矿层造成不可逆的化学腐蚀,影响钙钛矿太阳能电池的长期运行稳定性。在此,我们提出一种银配位诱导的[6,6]-苯基-C-丁酸甲酯n型掺杂策略,以保护银电极免受腐蚀,并阻止碘在PSC内的迁移。同时,DCBP与银之间的配位在PCBM层中诱导n型掺杂,加速了从钙钛矿层的电子提取。所得的PSC显示出26.03%的效率(认证效率为25.51%),非辐射电压损失最小,为126 mV。在一个太阳光照下连续进行2500小时最大功率点跟踪后,所得器件的PCE保持其初始值的95%,即使在85°C和85%相对湿度下加速老化1500小时后,仍保持其初始值的90%以上。