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通过新型间隔阳离子添加剂提高柔性钙钛矿太阳能电池的效率和稳定性。

Improved efficiency and stability of flexible perovskite solar cells by a new spacer cation additive.

作者信息

Zhang Xiaobo, Ma Yang, Chen Xiaoqing, Li Xuhong, Zhou Wencai, Ouedraogo Nabonswende Aida Nadege, Shirai Yasuhiro, Zhang Yongzhe, Yan Hui

机构信息

College of Material Sciences and Engineering, Beijing University of Technology Beijing 100124 China.

Key Laboratory of Optoelectronics Technology, Ministry of Education, Faculty of Information Technology, Beijing University of Technology Beijing 100124 China

出版信息

RSC Adv. 2021 Oct 14;11(53):33637-33645. doi: 10.1039/d1ra05399j. eCollection 2021 Oct 8.

DOI:10.1039/d1ra05399j
PMID:35497527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9042258/
Abstract

Flexible perovskite solar cells (PSCs) have attracted tremendous attention due to their potential application in portable and wearable electronics. However, the photoelectric conversion efficiency (PCE) of flexible PSCs is still far lower than that of usual rigid PSCs. Moreover, the mechanical stability of flexible PSCs cannot meet the needs of commercial applications because of the cracking of perovskite grains caused by bending stress. Here, we introduced a spacer cation additive (2-(chloromethyl) pyridine hydrochloride, CPHC) within the perovskite organic precursor to improve the device PCE and its mechanical stability. We observed that the CPHC spacer cation additive could simultaneously facilitate the crystallization of perovskite and stitch the grain boundaries to improve the flexibility. Compared to the 17.64% PCE of the control devices, the target flexible PSCs achieved a more highly efficiency over 19% with an improved mechanical stability (87.2% of the initial PCE after the 1000 cycles with the bending radius = 6 mm). In addition, compared to methylammonium or formamidinium cation, due to the stronger hydrophobic and larger activation energy barrier for the ion migration of the CPHC spacer cation, the device retained over 80% of the initial PCE after 30 days storage in an ambient environment.

摘要

柔性钙钛矿太阳能电池(PSCs)因其在便携式和可穿戴电子产品中的潜在应用而备受关注。然而,柔性PSCs的光电转换效率(PCE)仍远低于普通刚性PSCs。此外,由于弯曲应力导致钙钛矿晶粒开裂,柔性PSCs的机械稳定性无法满足商业应用的需求。在此,我们在钙钛矿有机前驱体中引入了一种间隔阳离子添加剂(2-(氯甲基)吡啶盐酸盐,CPHC),以提高器件的PCE及其机械稳定性。我们观察到,CPHC间隔阳离子添加剂可以同时促进钙钛矿的结晶并缝合晶界以提高柔韧性。与对照器件17.64%的PCE相比,目标柔性PSCs实现了超过19%的更高效率,且机械稳定性得到改善(在弯曲半径 = 6 mm的1000次循环后,初始PCE的87.2%)。此外,与甲铵或甲脒阳离子相比,由于CPHC间隔阳离子具有更强的疏水性和更大的离子迁移活化能垒,该器件在环境中储存30天后仍保留了超过80%的初始PCE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7f/9042258/9bf31a135449/d1ra05399j-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7f/9042258/9e9a75c02dc0/d1ra05399j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7f/9042258/9bf31a135449/d1ra05399j-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7f/9042258/9e9a75c02dc0/d1ra05399j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7f/9042258/9bf31a135449/d1ra05399j-f5.jpg

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本文引用的文献

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Bio-inspired vertebral design for scalable and flexible perovskite solar cells.生物启发的椎体设计,用于可扩展和灵活的钙钛矿太阳能电池。
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解析金属卤化物钙钛矿太阳能电池中的陷阱态的空间和能量分布。
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Mechanism of PbI in Situ Passivated Perovskite Films for Enhancing the Performance of Perovskite Solar Cells.PbI 原位钝化钙钛矿薄膜提高钙钛矿太阳能电池性能的机制。
ACS Appl Mater Interfaces. 2019 Nov 27;11(47):44101-44108. doi: 10.1021/acsami.9b13648. Epub 2019 Nov 13.
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Multifunctional Chemical Linker Imidazoleacetic Acid Hydrochloride for 21% Efficient and Stable Planar Perovskite Solar Cells.多功能化学连接剂盐酸咪唑乙酸用于 21%高效稳定的平面钙钛矿太阳能电池。
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Nanoscale Insights into Photovoltaic Hysteresis in Triple-Cation Mixed-Halide Perovskite: Resolving the Role of Polarization and Ionic Migration.三阳离子混合卤化物钙钛矿光伏滞后现象的纳米尺度洞察:解析极化和离子迁移的作用
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Pyridine-Terminated Conjugated Organic Molecules as an Interfacial Hole Transfer Bridge for NiO-Based Perovskite Solar Cells.吡啶端基共轭有机分子作为基于氧化镍的钙钛矿太阳能电池的界面空穴传输桥
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