串联
材料科学
钙钛矿(结构)
制作
能量转换效率
带隙
结晶度
退火(玻璃)
结晶
光电子学
纳米技术
化学工程
复合材料
病理
工程类
替代医学
医学
作者
Changlei Wang,Yue Zhao,Tianshu Ma,Yidan An,Rui He,Jing Wang,Cong Chen,Shengqiang Ren,Fan Fu,Dewei Zhao,Xiaofeng Li
出处
期刊:Nature Energy
[Springer Nature]
日期:2022-07-21
卷期号:7 (8): 744-753
被引量:136
标识
DOI:10.1038/s41560-022-01076-9
摘要
The broad bandgap tunability of organic–inorganic metal halide perovskites enables the fabrication of multi-junction all-perovskite tandem solar cells with ultra-high power conversion efficiencies (PCEs). Controllable crystallization plays a crucial role in the formation of high-quality perovskites. Here we report a universal close-space annealing strategy that increases grain size, enhances crystallinity and prolongs carrier lifetimes in low-bandgap (low-Eg) and wide-bandgap (wide-Eg) perovskite films. By placing the intermediate-phase perovskite films with their faces towards solvent-permeable covers during the annealing process, high-quality perovskite absorber layers are obtained with a slowed solvent releasing process, enabling fabrication of efficient single-junction perovskite solar cells (PVSCs) and all-perovskite tandem solar cells. As a result, the best PCEs of 21.51% and 18.58% for single-junction low-Eg and wide-Eg PVSCs are achieved and thus ensure the fabrication of 25.15% efficiency 4-terminal and 25.05% efficiency 2-terminal all-perovskite tandem solar cells. Controlling the crystallization of perovskites is not trivial. Here Wang et al. develop a close-space annealing to improve the structural and optoelectronic quality of perovskite films with different chemical compositions, leading to over 25% efficiency in all-perovskite tandem solar cells.
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