Sustainable thermal regulation improves stability and efficiency in all-perovskite tandem solar cells

被引:17
|
作者
Tan, Shuchen [1 ]
Li, Chongwen [2 ]
Peng, Cheng [1 ]
Yan, Wenjian [1 ]
Bu, Hongkai [1 ]
Jiang, Haokun [1 ]
Yue, Fang [1 ]
Zhang, Linbao [1 ]
Gao, Hongtao [1 ]
Zhou, Zhongmin [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[2] Univ Toronto, Dept Elect & Comp Engn, 35 St George St, Toronto, ON M5S 1A4, Canada
基金
中国国家自然科学基金;
关键词
LEAD IODIDE PEROVSKITES; TIN; METHYLAMMONIUM; CONDUCTIVITY; ELECTRONICS;
D O I
10.1038/s41467-024-48552-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mixed Sn-Pb perovskites have emerged as promising photovoltaic materials for both single- and multi-junction solar cells. However, achieving their scale-up and practical application requires further enhancement in stability. We identify that their poor thermal conductivity results in insufficient thermal transfer, leading to heat accumulation within the absorber layer that accelerates thermal degradation. A thermal regulation strategy by incorporating carboranes into perovskites is developed; these are electron-delocalized carbon-boron molecules known for their efficient heat transfer capability. We specifically select ortho-carborane due to its low thermal hysteresis. We observe its existence through the perovskite layer showing a decreasing trend from the buried interface to the top surface, effectively transferring heat and lowering the surface temperature by around 5 degrees C under illumination. o-CB also facilitates hole extraction at the perovskite/PEDOT:PSS interface and reduces charge recombination. These enable mixed Sn-Pb cells to exhibit improved thermal stability, retaining 80% of their initial efficiencies after aging at 85 degrees C for 1080hours. When integrated into monolithic all-perovskite tandems, we achieve efficiencies of over 27%. A tandem cell maintains 87% of its initial PCE after 704h of continuous operation under illumination.
引用
收藏
页数:9
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