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多功能添加剂实现的高耐久性倒置无机钙钛矿/有机串联太阳能电池

Highly Durable Inverted Inorganic Perovskite/Organic Tandem Solar Cells Enabled by Multifunctional Additives.

作者信息

Li Yanxun, Yan Yichao, Fu Yuang, Jiang Wenlin, Liu Ming, Chen Mingqian, Huang Xiaofeng, Lu Guanghao, Lu Xinhui, Yin Jun, Wu Shengfan, Jen Alex K-Y

机构信息

Department of Materials Science & Engineering, City University of Hong Kong, Kowloon, Hong Kong, 999077, China.

Hong Kong Institute for Clean Energy, City University of Hong Kong, Kowloon, Hong Kong, 999077, China.

出版信息

Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202412515. doi: 10.1002/anie.202412515. Epub 2024 Oct 17.

DOI:10.1002/anie.202412515
PMID:39155244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11656153/
Abstract

Inverted perovskite/organic tandem solar cells (P/O TSCs) suffer from poor long-term device stability due to halide segregation in organic-inorganic hybrid wide-band gap (WBG) perovskites, which hinders their practical deployment. Therefore, developing all-inorganic WBG perovskites for incorporation into P/O TSCs is a promising strategy because of their superior stability under continuous illumination. However, these inorganic WBG perovskites also face some critical issues, including rapid crystallization, phase instability, and large energy loss, etc. To tackle these issues, two multifunctional additives based on 9,10-anthraquinone-2-sulfonic acid (AQS) are developed to regulate the perovskite crystallization by mediating the intermediate phases and suppress the halide segregation through the redox-shuttle effect. By coupling with organic cations having the desirable functional groups and dipole moments, these additives can effectively passivate the defects and adjust the alignment of interface energy levels. Consequently, a record V approaching 1.3 V with high power conversion efficiency (PCE) of 18.59 % could be achieved in a 1.78 eV band gap single-junction inverted all-inorganic PSC. More importantly, the P/O TSC derived from this cell demonstrates a T lifetime of 1000 h under continuous operation, presenting the most stable P/O TSCs reported so far.

摘要

倒置钙钛矿/有机串联太阳能电池(P/O TSCs)由于有机-无机混合宽带隙(WBG)钙钛矿中的卤化物偏析,长期器件稳定性较差,这阻碍了它们的实际应用。因此,开发用于P/O TSCs的全无机WBG钙钛矿是一种很有前景的策略,因为它们在持续光照下具有优异的稳定性。然而,这些无机WBG钙钛矿也面临一些关键问题,包括快速结晶、相不稳定和能量损失大等。为了解决这些问题,开发了两种基于9,10-蒽醌-2-磺酸(AQS)的多功能添加剂,通过介导中间相来调节钙钛矿结晶,并通过氧化还原穿梭效应抑制卤化物偏析。通过与具有所需官能团和偶极矩的有机阳离子偶联,这些添加剂可以有效地钝化缺陷并调整界面能级的排列。因此,在带隙为1.78 eV的单结倒置全无机PSC中,可以实现接近1.3 V的创纪录开路电压(V)和18.59%的高功率转换效率(PCE)。更重要的是,由该电池衍生的P/O TSC在连续运行下的T寿命为1000小时,是迄今为止报道的最稳定的P/O TSCs。

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Adv Mater. 2024 Jun;36(23):e2312237. doi: 10.1002/adma.202312237. Epub 2024 Mar 8.
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