Amphiphilic Carbon Dots Suppress Iodide Ion Migration in Perovskite Solar Cells

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*, Andrey L. Rogach*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

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. © 2025 American Chemical Society.
Original languageEnglish
Pages (from-to)8261–8272
JournalEnergy and Fuels
Volume39
Issue number17
Online published17 Apr 2025
DOIs
Publication statusPublished - 1 May 2025

Funding

This research was supported by the Priority 2030 Federal Academic Leadership Program, the Global Experts project funded by the Moravian-Silesian Region and VSB-TUO (contract 00734/2023/RRC), and the Russian Science Foundation (project 24-62-00022) for the part related to the solar cell characterization. XPS studies were performed on equipment of the Resource Center \u201CPhysical Methods of Surface Investigation\u201D of the Scientific Park of St. Petersburg State University. The authors express their gratitude to the ITMO University Core Facility Center \u201CNanotechnologies\u201D.

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