钙钛矿(结构)
钝化
材料科学
串联
结晶
硅
晶界
能量转换效率
载流子寿命
退火(玻璃)
化学工程
光电子学
纳米技术
复合材料
图层(电子)
微观结构
工程类
作者
Oussama Er‐raji,Mohamed A. A. Mahmoud,Oliver Fischer,Alexandra J. Ramadan,Dmitry Bogachuk,A. Reinholdt,A. Schmitt,Bhushan P. Kore,Thomas W. Gries,Artem Musiienko,Oliver Schultz‐Wittmann,Martin Bivour,Martin Hermle,Martin C. Schubert,Juliane Borchert,Stefan W. Glunz,Patricia S. C. Schulze
出处
期刊:Joule
[Elsevier]
日期:2024-07-01
被引量:2
标识
DOI:10.1016/j.joule.2024.06.018
摘要
Fully textured perovskite silicon tandem solar cells are promising for future low-cost photovoltaic deployment. However, the fill factor and open-circuit voltage of these devices are currently limited by the high density of defects at grain boundaries and at interfaces with charge transport layers. To address this, we devise a strategy to simultaneously enhance perovskite crystallization and passivate the perovskite/C60 interface. By incorporating urea (CO(NH2)2) as an additive in the solution step of the hybrid evaporation/spin-coating perovskite deposition method, the crystallization kinetics are accelerated, leading to the formation of the desired photoactive phase at room temperature. With that, perovskite films with large grain sizes (>1 μm) and improved optoelectronic quality are formed at low annealing temperatures (100°C). Concurrently, remnant urea molecules are expelled at the perovskite surface, which locally displaces the C60 layer, thus reducing interfacial non-radiative recombination losses. With this strategy, the resulting tandem solar cells achieve 30.0% power conversion efficiency.
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