材料科学
光电流
光活性层
钙钛矿(结构)
聚合物太阳能电池
能量转换效率
异质结
薄膜
光电子学
载流子
活动层
磁滞
带隙
化学工程
纳米技术
图层(电子)
薄膜晶体管
工程类
物理
量子力学
作者
Lening Shen,Tao Zhu,Xinwen Zhang,Keven Gong,He Wang,Xiong Gong
出处
期刊:Nano Energy
[Elsevier BV]
日期:2022-01-03
卷期号:93: 106907-106907
被引量:25
标识
DOI:10.1016/j.nanoen.2021.106907
摘要
Perovskite solar cells (PSCs) as alternative cost-effective solar technology have drawn great concentrations in both academic and industrial sectors in the past years. Through the film morphological manipulation of perovskite photoactive layers and generic interfacial engineering, efficient PSCs have been reported. However, intrinsic unbalanced charge transport within the perovskite photoactive layer, which restricted further boost device performance of PSCs, was not fully addressed. In this study, we report high-performance bulk heterojunction (BHJ) PSCs based on the composites composed of n-type Cs 0.15 FA 0.85 PbI 3 (where FA is formamidinium, HC(NH 2 ) 2 ) incorporated with p-type low optical gap conjugated polymer. Compared to pristine Cs 0.15 FA 0.85 PbI 3 thin film, the BHJ composite thin film possesses enhanced and balanced charge carrier mobilities, enlarged crystal sizes, and suppressed non-radiation charge carrier recombination. Most importantly, a photo-induced charge transfer occurs within the BHJ composite thin film. As a result, the BHJ PSCs exhibit a power conversion efficiency (PCE) of 21.08%. In addition, un-encapsulated BHJ PSCs possess remarkably enhanced stability (as they retain 80% of their initial PCE after ~ 200 days in ambient conditions) and diminished photocurrent hysteresis (photocurrent hysteresis index of 0.012) compared to those based on pristine Cs 0.15 FA 0.85 PbI 3 thin film. All these results demonstrate that the PSCs with a BHJ device structure are one of the facile ways to approach high-performance PSCs. Bulk heterojunction perovskite solar cells based on n-type Cs 0.15 FA 0.85 PbI 3 (where FA is formamidinium) incorporated with p-type low optical gap conjugated polymer exhibited 21.8% of power conversion efficiency (PCE), and in addition, un-encapsulated cells retained 80% of their initial PCE after ~ 200 days in ambient conditions and diminished photocurrent hysteresis (photocurrent hysteresis index of 0.012). • n-type perovskites mixed with p-type low optical gap conjugated polymers forming bulk heterojunction (BHJ) composites. • Enhanced and balanced charge carrier mobilities, enlarged crystal sizes, and suppressed non-radiative charge carrier recombination observed from BHJ composite. • Photo-induced charge transfer occurs within BHJ composites. • BHJ perovskite solar cells (PSCs) exhibit a power conversion efficiency (PCE) of 21.08%. • Un-encapsulated BHJ PSCs possess remarkably enhanced stability and dramatically suppressed photocurrent hysteresis compared to PSCs based on pristine perovskite thin film.
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