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通过电子传输层工程实现CsPbI钙钛矿量子点太阳能电池的降解抑制与性能增强

Suppressed Degradation and Enhanced Performance of CsPbI Perovskite Quantum Dot Solar Cells via Engineering of Electron Transport Layers.

作者信息

Lim S, Kim J, Park J Y, Min J, Yun S, Park T, Kim Y, Choi J

机构信息

Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.

Department of Chemical Engineering, Hanyang University, Seoul 04763, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2021 Feb 10;13(5):6119-6129. doi: 10.1021/acsami.0c15484. Epub 2021 Jan 27.

DOI:10.1021/acsami.0c15484
PMID:33499586
Abstract

CsPbI perovskite quantum dots (CsPbI-PQDs) have recently come into focus as a light-harvesting material that can act as a platform through which to combine the material advantages of both perovskites and QDs. However, the low cubic-phase stability of CsPbI-PQDs in ambient conditions has been recognized as a factor that inhibits device stability. TiO nanoparticles are the most regularly used materials as an electron transport layer (ETL) in CsPbI-PQD photovoltaics; however, we found that TiO can facilitate the cubic-phase degradation of CsPbI-PQDs due to its vigorous photocatalytic activity. To address these issues, we have developed chloride-passivated SnO QDs (Cl@SnO QDs), which have low photocatalytic activity and few surface traps, to suppress the cubic-phase degradation of CsPbI-PQDs. Given these advantages, the CsPbI-PQD solar cells based on Cl@SnO ETLs show significantly improved device operational stability (under conditions of 50% relative humidity and 1-sun illumination), compared to those based on TiO ETLs. In addition, the Cl@SnO-based devices showed improved open circuit voltage and photocurrent density, resulting in enhanced power conversion efficiency (PCE) up to 14.5% compared to that of TiO-based control devices (PCE of 13.8%).

摘要

CsPbI钙钛矿量子点(CsPbI-PQDs)最近作为一种光捕获材料受到关注,它可以作为一个平台,将钙钛矿和量子点的材料优势结合起来。然而,CsPbI-PQDs在环境条件下立方相稳定性低已被认为是抑制器件稳定性的一个因素。TiO纳米颗粒是CsPbI-PQD光伏器件中最常用的电子传输层(ETL)材料;然而,我们发现TiO因其强烈的光催化活性会促进CsPbI-PQDs的立方相降解。为了解决这些问题,我们开发了氯化物钝化的SnO量子点(Cl@SnO QDs),其具有低光催化活性和少量表面陷阱,以抑制CsPbI-PQDs的立方相降解。鉴于这些优点,与基于TiO ETL的器件相比,基于Cl@SnO ETL的CsPbI-PQD太阳能电池在器件运行稳定性方面有显著提高(在50%相对湿度和1个太阳光照条件下)。此外,基于Cl@SnO的器件显示出开路电压和光电流密度的提高,与基于TiO的对照器件(PCE为13.8%)相比,功率转换效率(PCE)提高到了14.5%。

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