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用于钙钛矿太阳能电池的低维钙钛矿钝化层的阴阳离子协同调控

Anion-Cation Synergistic Regulation of Low-Dimensional Perovskite Passivation Layer for Perovskite Solar Cells.

作者信息

Li Shengwen, Gu Hao, Zhu Annan, Guo Jia, Xi Chenpeng, Qiu Xiaosong, Chen Ying, Pan Hui, Chen Jiangzhao, Xing Guichuan, Chen Shi

机构信息

Institute of Applied Physics and Materials Engineering, University of Macau, Taipa, Macao, 999078, China.

Faulty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming, China.

出版信息

Adv Mater. 2025 Jul;37(28):e2500988. doi: 10.1002/adma.202500988. Epub 2025 Apr 24.

DOI:10.1002/adma.202500988
PMID:40270282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12272002/
Abstract

Mixing 2D and 3D perovskite together is an effective strategy to enhance the stability of perovskite solar cells (PSCs). This strategy has been widely used in many recent works. Typically, 2D layer is formed by introducing 2D spacer onto 3D surfaces through in situ intercalation reaction. However, this intercalation may not stop after the 2D layer is formed. Progressive migration of 2D spacer into 3D bulk leads to increased n-values of 2D phases and deviation from optimized structural design. The high n-value 2D perovskite is less stable than the low n-value 2D perovskite and may be prone to degradation under external stresses. Here, a heteroatom ammonium ligand, thiomorpholine (SMOR) is found, which can effectively passivate the perovskite surface, and form a 1D phase or 2D phase depending on cation to anion ratio and the type of anions. Due to lower formation energy at 1:1 cation to anion ratio, 1D phase can prevent the formation of high-n-value 2D phase and show excellent thermal stability. The passivation of SMOR-based 1D perovskite boosts the device efficiency to 25.6% (certified 24.7%). More importantly, the unpackaged device can maintain >80% of its initial efficiency after stable operation at 85 °C for 1000 h.

摘要

将二维和三维钙钛矿混合在一起是提高钙钛矿太阳能电池(PSC)稳定性的有效策略。这一策略在最近的许多研究中都得到了广泛应用。通常,二维层是通过原位插层反应将二维间隔物引入三维表面而形成的。然而,这种插层在二维层形成后可能不会停止。二维间隔物向三维主体的逐步迁移会导致二维相的n值增加,并偏离优化的结构设计。高n值的二维钙钛矿比低n值的二维钙钛矿稳定性差,在外部应力下可能容易降解。在此,发现了一种杂原子铵配体,硫代吗啉(SMOR),它可以有效地钝化钙钛矿表面,并根据阳离子与阴离子的比例和阴离子的类型形成一维相或二维相。由于阳离子与阴离子比例为1:1时形成能较低,一维相可以防止高n值二维相的形成,并表现出优异的热稳定性。基于SMOR的一维钙钛矿的钝化将器件效率提高到了25.6%(认证效率为24.7%)。更重要的是,未封装的器件在85℃稳定运行1000小时后,可以保持其初始效率的80%以上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/b274f9552dc2/ADMA-37-2500988-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/ceb601b9f4db/ADMA-37-2500988-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/1ed87df22af0/ADMA-37-2500988-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/84940ef168d9/ADMA-37-2500988-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/09f1a7c00200/ADMA-37-2500988-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/b274f9552dc2/ADMA-37-2500988-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/ceb601b9f4db/ADMA-37-2500988-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/1ed87df22af0/ADMA-37-2500988-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/84940ef168d9/ADMA-37-2500988-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/09f1a7c00200/ADMA-37-2500988-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0041/12272002/b274f9552dc2/ADMA-37-2500988-g001.jpg

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