钙钛矿(结构)
材料科学
串联
光伏
硅
化学工程
聚合物
离子键合
光电子学
纳米技术
离子
化学
光伏系统
有机化学
复合材料
工程类
生态学
生物
作者
Lu Liu,Bita Farhadi,Jianxun Li,Siyi Liu,Linfeng Lu,Hui Wang,Minyong Du,Liyou Yang,Shaojuan Bao,Jiang Xiao,Xinrui Dong,Qingqing Miao,Dongdong Li,Kai Wang,Shengzhong Liu
标识
DOI:10.1002/anie.202317972
摘要
Abstract The pursuit of highly efficient and stable wide‐band gap (WBG) perovskite solar cells (PSCs), especially for monolithic perovskite/silicon tandem devices, is a key focus in achieving the commercialization of perovskite photovoltaics. In this study, we initially designed poly(ionic liquid)s (PILs) with varying alkyl chain lengths based on density functional theory calculations. Results pinpoint that PILs with longer alkyl chain lengths tend to exhibit more robust binding energy with the perovskite structure. Then we synthesized the PILs to craft a hydrophobic hydrogen‐bonded polymer network (HHPN) that passivates the WBG perovskite/electron transport layer interface, inhibits ion migration and serves as a barrier layer against water and oxygen ingression. Accordingly, the HHPN effectively curbs nonradiative recombination losses while facilitating efficient carrier transport, resulting in substantially enhanced open‐circuit voltage ( V oc ) and fill factor. As a result, the optimized single‐junction WBG PSC achieves an impressive efficiency of 23.18 %, with V oc as high as 1.25 V, which is the highest reported for WBG (over 1.67 eV) PSCs. These devices also demonstrate outstanding thermostability and humidity resistance. Notably, this versatile strategy can be extended to textured perovskite/silicon tandem cells, reaching a remarkable efficiency of 28.24 % while maintaining exceptional operational stability.
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