利用多功能自组装单层优化埋藏界面增强锡基钙钛矿太阳能电池的电荷收集。

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Materials & Interfaces Pub Date : 2025-04-02 Epub Date: 2025-03-20 DOI:10.1021/acsami.5c01653
Junyu Qu, Xiaoxue Wang, Chuan Luo, Chenwu Zeng, Hangyu Zhou, Zihao Yang, Zhihao Zhang, Jialun Jin, Yuanfang Huang, Chao Ding, Cong Chen, Shengqiang Ren, Dewei Zhao
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引用次数: 0

摘要

聚(3,4-乙烯二氧噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)是一种广泛应用于倒置锡基钙钛矿太阳能电池(Sn-PSCs)的空穴传输材料。然而,这些利用PEDOT:PSS的sn - psc的效率和稳定性并不令人满意,部分原因是担心它们的工作功能不匹配、疏水性和化学相互作用。本文在PEDOT:PSS/Sn钙钛矿界面上引入自组装单层(SAM) (2-(7h -二苯并[c,g]咔唑-7-基)乙基)膦酸(2PADCB)作为多功能缓冲分子。在PEDOT:PSS中,2PADCB分子中的磷酸基与噻吩环上的硫原子发生反应。该反应过程有效地将SAM分子牢牢地固定在PEDOT:PSS表面。此外,它减少了PEDOT与PSS之间的结合位点,减轻了PEDOT:PSS表面的酸化和PSS过量导致的导电性差。此外,在2PADCB分子末端基团上另外两个苯环的存在增加了Sn2+周围的电子密度,从而抑制了Sn2+的氧化。此外,2PADCB分子的疏水特性减轻了PEDOT:PSS的水分渗透,从而保护了Sn钙钛矿的降解。因此,基于PEDOT:PSS/2PADCB薄膜的sn - psc获得了14.7%的冠军效率,高于原始材料(12.5%)。此外,2PADCB分子提高了器件的稳定性,在1个太阳照射160小时后保持90%的初始效率。这种效率和稳定性的提高主要是由于与2PADCB分子的界面质量得到改善,从而导致在PEDOT:PSS/Sn钙钛矿界面上更好的载流子传输和抑制电荷重组。我们的工作表明,在PEDOT:PSS/钙钛矿界面引入2PADCB分子是制备高效稳定的Sn-PSCs的一种很有前途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing Charge Collection of Tin-Based Perovskite Solar Cells by Optimizing the Buried Interface with a Multifunctional Self-Assembled Monolayer.

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a widely used hole transport material in inverted tin-based perovskite solar cells (Sn-PSCs). However, the efficiency and stability of these Sn-PSCs that utilize PEDOT:PSS are unsatisfactory, partly due to concerns about their mismatched work functions, hydrophobicity, and chemical interactions. Here, we introduce a self-assembled monolayer (SAM), (2-(7H-dibenzo[c,g]carbazol-7-yl)ethyl) phosphonic acid (2PADCB) as a multifunctional buffer molecule at the buried PEDOT:PSS/Sn perovskite interface. The phosphate group in the 2PADCB molecule reacts with the sulfur atom on the thiophene ring in PEDOT:PSS. This reaction process effectively anchors the SAM molecule firmly to the surface of PEDOT:PSS. Additionally, it reduces the binding sites between PEDOT and PSS, alleviating the acidification of the PEDOT:PSS surface and the poor conductivity caused by excessive PSS. Furthermore, the presence of two additional benzene rings in the 2PADCB molecule terminal group increases the electron density around Sn2+, thereby inhibiting its oxidation. Additionally, the hydrophobic characteristics of the 2PADCB molecule mitigate moisture infiltration from PEDOT:PSS, thereby protecting the degradation of Sn perovskite. Consequently, the Sn-PSCs based on the PEDOT:PSS/2PADCB film achieve a champion efficiency of 14.7%, higher than that of their pristine counterpart (12.5%). Moreover, the 2PADCB molecule improves the stability of the device by maintaining 90% of its initial efficiency after 160 h under 1 Sun illumination. Such enhancement in efficiency and stability is mainly attributed to the improved interface quality with the 2PADCB molecule, leading to better carrier transport and suppressed charge recombination at the buried PEDOT:PSS/Sn perovskite interface. Our work suggests that introducing the 2PADCB molecule at the PEDOT:PSS/perovskite interface is a promising method for efficient and stable Sn-PSCs.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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