Qu Shujie, Huang Hao, Wang Jinhui, Cui Peng, Li Yiyi, Wang Min, Li Liang, Yang Fu, Sun Changxu, Zhang Qiang, Zhu Pengkun, Wang Yi, Li Meicheng
State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206, China.
Key Laboratory of Advanced Light Conversion Materials and Biophotonics, School of Chemistry and Life Resources Institution, Renmin University of China, Beijing, 100872, China.
Angew Chem Int Ed Engl. 2025 Jan 21;64(4):e202415949. doi: 10.1002/anie.202415949. Epub 2024 Nov 2.
Ion migration is a major issue hindering the long-term stability of perovskite solar cells (PSCs). As an intrinsic characteristic of metal halide perovskite materials, ion migration is closely related to the atomic arrangement and coordination, which are the basic characteristic differences among various facets. Herein, we report the facet-related ion migration, and then achieve the inhibition of ion migration in perovskite through finely modulating the facet orientation. We show that the (100) facet is substantially more vulnerable to cationic migration than the (111) facet. The main reason for this difference in migration is that the cationic migration route in the (111) facet deviates from that in the (100) facet, which increases the active migration energy and weakens the contribution from the electric field during operation. We prepare a (111)-dominated perovskite film by incorporating a facile and green addition of water (HO) into the antisolvent, further achieving a power conversion efficiency (PCE) of 26.0 % (25.4 % certification) on regular planar PSCs and 25.8 % on inverted PSCs. Moreover, the unencapsulated PSCs can maintain 95 % of their initial PCE after 3500-hours operation under simulated AM1.5 illumination at the maximum power point.
离子迁移是阻碍钙钛矿太阳能电池(PSC)长期稳定性的一个主要问题。作为金属卤化物钙钛矿材料的固有特性,离子迁移与原子排列和配位密切相关,而原子排列和配位是不同晶面之间的基本特征差异。在此,我们报道了与晶面相关的离子迁移,然后通过精细调节晶面取向实现了对钙钛矿中离子迁移的抑制。我们表明,(100)晶面比(111)晶面更容易发生阳离子迁移。这种迁移差异的主要原因是(111)晶面中的阳离子迁移路径与(100)晶面中的不同,这增加了有效迁移能量并削弱了运行过程中电场的贡献。我们通过在反溶剂中加入简便且绿色的水(HO)制备了以(111)为主的钙钛矿薄膜,在常规平面PSC上进一步实现了26.0%的功率转换效率(PCE)(认证值为25.4%),在倒置PSC上实现了25.8%的PCE。此外,未封装的PSC在模拟AM1.5光照下最大功率点运行3500小时后,仍能保持其初始PCE的95%。