铷
串联
钙钛矿(结构)
纳米技术
材料科学
化学
结晶学
钾
有机化学
复合材料
作者
Xufeng Liao,Xuefei Jia,Weisheng Li,Xiting Lang,Jianhua Zhang,Xinyu Zhao,Yitong Ji,Qingguo Du,Chun‐Hsiao Kuan,Zhiwei Ren,Wenchao Huang,Yang Bai,Kaicheng Zhang,Chuanxiao Xiao,Qianqian Lin,Yi‐Bing Cheng,Jinhui Tong
标识
DOI:10.1038/s41467-025-56549-8
摘要
All-perovskite tandem solar cells (APTSCs) offer the potential to surpass the Shockley-Queisser limit of single-junction solar cells at low cost. However, high-performance APTSCs contain unstable methylammonium (MA) cation in the tin-lead (Sn-Pb) narrow bandgap subcells. Currently, MA-free Sn-Pb perovskite solar cells (PSCs) show lower performance compared with their MA-containing counterparts. This is due to the high trap density associated with Sn2+ oxidation, which is exacerbated by the rapid crystallization of MA-free Sn-containing perovskite. Here, a multifunctional additive rubidium acetate (RbAC) is proposed to passivate Sn-Pb perovskite. We find that RbAC can suppress Sn2+ oxidation, alleviate microstrain, and improve the crystallinity of the MA-free Sn-Pb perovskite. Consequently, the resultant Sn-Pb PSCs achieve a power conversion efficiency (PCE) of 23.02%, with an open circuit voltage (Voc) of 0.897 V, and a filling factor (FF) of 80.64%, and more importantly the stability of the device is significantly improved. When further integrated with a 1.79-electron volt MA-free wide-bandgap PSC, a 29.33% (certified 28.11%) efficient MA-free APTSCs with a high Voc of 2.22 volts is achieved. The high trap density associated with tin (II) oxidation impacts the device performance of methylammonium cation-free tin-lead perovskite solar cells. Here, authors employ rubidium acetate for defect passivation and achieve efficient and stable single-junction and all-perovskite tandem solar cells.
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