Mixed tin-lead perovskites with balanced crystallization and oxidation barrier for all-perovskite tandem solar cells

串联 钙钛矿(结构) 结晶 材料科学 三碘化物 化学工程 纳米技术 化学 冶金 复合材料 电极 工程类 物理化学 色素敏化染料 电解质
作者
Jin Zhou,Shiqiang Fu,Shun Zhou,Lishuai Huang,Cheng Wang,Hongling Guan,Dexin Pu,Hongsen Cui,Chen Wang,Ti Wang,Weiwei Meng,Guojia Fang,Weijun Ke
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:15 (1): 2324-2324 被引量:143
标识
DOI:10.1038/s41467-024-46679-w
摘要

Abstract Mixed tin-lead perovskite solar cells have driven a lot of passion for research because of their vital role in all-perovskite tandem solar cells, which hold the potential for achieving higher efficiencies compared to single-junction counterparts. However, the pronounced disparity in crystallization processes between tin-based perovskites and lead-based perovskites, coupled with the easy Sn 2+ oxidation, has long been a dominant factor contributing to high defect densities. In this study, we propose a multidimensional strategy to achieve efficient tin-lead perovskite solar cells by employing a functional N-(carboxypheny)guanidine hydrochloride molecule. The tailored N-(carboxypheny)guanidine hydrochloride molecule plays a pivotal role in manipulating the crystallization and grain growth of tin-lead perovskites, while also serving as a preservative to effectively inhibit Sn 2+ oxidation, owing to the strong binding between N-(carboxypheny)guanidine hydrochloride and tin (II) iodide and the elevated energy barriers for oxidation. Consequently, single-junction tin-lead cells exhibit a stabilized power conversion efficiency of 23.11% and can maintain 97.45% of their initial value even after 3500 h of shelf storage in an inert atmosphere without encapsulation. We further integrate tin-lead perovskites into two-terminal monolithic all-perovskite tandem cells, delivering a certified efficiency of 27.35%.
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