两亲性碳点抑制钙钛矿太阳能电池中碘离子的迁移

IF 5.3 3区 工程技术 Q2 ENERGY & FUELS
Igor V. Margaryan, Egor D. Ogorodnikov, Mikhail D. Miruschenko, Anastasiia V. Sokolova, Vladimir S. Ivanov, Guangbo Zhou, Aleksandra V. Koroleva, Evgeniy V. Zhizhin, Sergey V. Makarov, Aleksandr P. Litvin, Elena V. Ushakova* and Andrey L. Rogach*, 
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引用次数: 0

摘要

尽管卤化铅钙钛矿太阳能电池(PSCs)在功率转换效率(PCE)方面取得了相当大的进步,但其运行耐久性仍然是其广泛商业化的关键挑战。PSC不稳定性的主要来源之一是钙钛矿层中的卤化物阴离子迁移,导致钙钛矿晶体结构缺乏稳定性,特别是当温度和湿度升高时,这会导致PCE降低。通过PSC结构的改进,可以消除不希望的离子迁移。例如,适当设计电子和空穴传输层,以及在钙钛矿层中加入碳点(CDs)等纳米颗粒添加剂。该研究表明,带负电荷的两亲性CDs表面含有许多脂肪族、羰基和羟基,可以有效抑制碘化物的迁移过程,从而提高基于FACsPbI3 (FA停留在甲酰胺阳离子上)的psc的性能和稳定性。这些CD添加剂的引入影响了FACsPbI3钙钛矿薄膜的结晶过程,导致钙钛矿晶粒尺寸增加了81%,同时与没有CD的参考样品相比,减少了不需要的PbI2相的外观。此外,将CDs掺入钙钛矿薄膜使我们能够调整其能级结构,促进psc中的载流子提取。结果,基于两亲性聚乙二醇覆盖cd的FACsPbI3钙钛矿薄膜的psc显示出最大短路电流的增加和正向和反向扫描之间的滞后抑制。后一种效应归因于缺陷的钝化,这导致离子迁移途径的减少和电子传输层和钙钛矿活性层之间界面上的I -阴离子的数量。这些改进使这种psc的最大PCE为15%,与没有任何cd的参考设备的最大PCE值相比,提高了29%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Amphiphilic Carbon Dots Suppress Iodide Ion Migration in Perovskite Solar Cells

Amphiphilic Carbon Dots Suppress Iodide Ion Migration in Perovskite Solar Cells

Despite considerable advancements in the power conversion efficiency (PCE) of lead halide perovskite solar cells (PSCs), their operational durability remains a pivotal challenge for their widespread commercialization. One of the primary sources of instability of PSCs is the halide anion migration in the perovskite layer, causing a lack of stability of the perovskite crystal structure, particularly when subjected to increased temperature and moisture, which results in reduction in the PCE. Undesirable ion migration can be eliminated through advancements in PSC architecture, such as proper design of electron and hole transport layers and incorporation of nanoparticle additives such as carbon dots (CDs) into the perovskite layer. This study has shown that negatively charged amphiphilic CDs with many aliphatic, carbonyl, and hydroxyl groups at the surface are effective in suppressing the iodide migration process and thus improve the performance and stability of PSCs based on FACsPbI3 (FA stays for the formamidinium cation). Introduction of these CD additives affects the crystallization process of FACsPbI3 perovskite films, causing an increase of the perovskite grain size by 81% and at the same time a diminished appearance of the undesired PbI2 phase as compared to the reference sample without CDs. Furthermore, incorporation of CDs into perovskite films enables us to adjust their energy level structure, facilitating charge carrier extraction in PSCs. As a result, PSCs based on the FACsPbI3 perovskite films with amphiphilic poly(ethylene glycol)-covered CDs demonstrate an increase in the maximum short-circuit current and suppressed hysteresis between forward and reverse scans. The latter effect is attributed to the passivation of defects, which results in the reduction of the ion migration pathways and the amount of I anions at the interface between the electron transport layer and the perovskite active layer. These improvements result in a maximum PCE of such PSCs of 15%, which is 29% higher as compared to the maximum value of PCE for the reference device without any CDs.

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来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
期刊介绍: Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.
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