In situ Blending For Co-Deposition of Electron Transport and Perovskite Layers Enables Over 24% Efficiency Stable Inverted Solar Cells

被引:3
|
作者
Wang, Wanhai [1 ,2 ]
Li, Xiaofeng [2 ]
Huang, Pengyu [1 ]
Yang, Li [2 ,3 ]
Gao, Liang [1 ]
Jiang, Yonghe [1 ]
Hu, Jianfei [2 ]
Gao, Yinhu [2 ]
Che, Yuliang [2 ]
Deng, Jidong [2 ]
Zhang, Jinbao [2 ,3 ]
Tang, Weihua [1 ,2 ,3 ]
机构
[1] Xiamen Univ, Inst Flexible Elect IFE, Coll Mat, Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Mat, Fujian Key Lab Adv Mat, Xiamen Key Lab Elect Ceram Mat & Devices, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金;
关键词
co-deposition; electron transport layer; in situ blending; perovskite solar cell; GENERATION;
D O I
10.1002/adma.202407349
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Simplifying the manufacturing processes of multilayered high-performance perovskite solar cells (PSCs) is yet of vital importance for their cost-effective production. Herein, an in situ blending strategy is presented for co-deposition of electron transport layer (ETL) and perovskite absorber by incorporating (3-(7-butyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo- [lmn][3,8]phenanthrolin-2(1H)-yl)propyl)phosphonic acid (NDP) into the perovskite precursor solutions. The phosphonic acid-like anchoring group coupled with its large molecular size drives the migration of NDP toward indium tin oxide (ITO) surface to form a distinct ETL during perovskite film forming. This strategy circumvents the critical wetting issue and simultaneously improves the interfacial charge collection efficiencies. Consequently, n-i-p PSCs based on in situ blended NDP achieve a champion power conversion efficiency (PCE) of 24.01%, which is one of the highest values for PSCs using organic ETLs. This performance is notably higher than that of ETL-free (21.19%) and independently spin-coated (21.42%) counterparts. More encouragingly, the in situ blending strategy dramatically enhances the device stability under harsh conditions by retaining over 90% of initial efficiencies after 250 h in 100 degrees C or 65% humidity storage. Moreover, this strategy is universally adaptable to various perovskite compositions, device architectures, and electron transport materials (ETMs), showing great potential for applications in diverse optoelectronic devices. Electron transport layer (ETL) materials have been rationally designed for in situ blending to co-deposit ETL and light-absorbing layers simultaneously in inverted perovskite solar cells. Such a strategy significantly improves the qualities of perovskite growth and buried interface to improve charge transport/collection. A record high power conversion efficiency over 24% is achieved for organic ETLs based devices. image
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页数:10
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