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本文引用的文献

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Design of Intrinsically Stable Hole-Selective Self-Assembled Monolayers by Introducing Fused-Ring Intramolecular Donor-Acceptor Interactions.
Angew Chem Int Ed Engl. 2025 Jul 7;64(28):e202507273. doi: 10.1002/anie.202507273. Epub 2025 May 12.
2
Management of Intramolecular Noncovalent Interactions in Dopant-Free Hole Transport Materials for High-Performance Perovskite Solar Cells.用于高性能钙钛矿太阳能电池的无掺杂空穴传输材料中分子内非共价相互作用的管理
Angew Chem Int Ed Engl. 2025 May 26;64(22):e202504144. doi: 10.1002/anie.202504144. Epub 2025 Apr 2.
3
Enlarging moment and regulating orientation of buried interfacial dipole for efficient inverted perovskite solar cells.通过增大埋入界面偶极矩并调整其取向来制备高效倒置钙钛矿太阳能电池。
Nat Commun. 2025 Feb 1;16(1):1252. doi: 10.1038/s41467-024-55653-5.
4
Reinforcing Coverage of Self-assembled Monomolecular Layers for Inverted Perovskite Solar Cells with Efficiency of 25.70 .增强用于效率为25.70%的倒置钙钛矿太阳能电池的自组装单分子层的覆盖度
Angew Chem Int Ed Engl. 2025 Mar 24;64(13):e202423827. doi: 10.1002/anie.202423827. Epub 2025 Jan 10.
5
Stabilization Strategies of Buried Interface for Efficient SAM-Based Inverted Perovskite Solar Cells.用于高效基于自组装单分子层的倒置钙钛矿太阳能电池的掩埋界面稳定策略
Angew Chem Int Ed Engl. 2025 Jan 21;64(4):e202419608. doi: 10.1002/anie.202419608. Epub 2024 Dec 4.
6
Stereo-Hindrance Induced Conformal Self-Assembled Monolayer for High Efficiency Inverted Perovskite Solar Cells.用于高效倒置钙钛矿太阳能电池的立体位阻诱导共形自组装单分子层
Small. 2024 Dec;20(52):e2407387. doi: 10.1002/smll.202407387. Epub 2024 Nov 6.
7
Efficient wide-bandgap perovskite photovoltaics with homogeneous halogen-phase distribution.具有均匀卤素相分布的高效宽带隙钙钛矿光伏电池。
Nat Commun. 2024 Oct 16;15(1):8899. doi: 10.1038/s41467-024-53344-9.
8
Co-adsorbed self-assembled monolayer enables high-performance perovskite and organic solar cells.共吸附自组装单分子层可实现高性能钙钛矿和有机太阳能电池。
Nat Commun. 2024 Sep 1;15(1):7605. doi: 10.1038/s41467-024-51760-5.
9
Enhancing Hole Transport Uniformity for Efficient Inverted Perovskite Solar Cells through Optimizing Buried Interface Contacts and Suppressing Interface Recombination.通过优化掩埋界面接触和抑制界面复合来提高高效倒置钙钛矿太阳能电池的空穴传输均匀性
Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202412601. doi: 10.1002/anie.202412601. Epub 2024 Oct 22.
10
Recent Advances in Carbazole-Based Self-Assembled Monolayer for Solution-Processed Optoelectronic Devices.用于溶液处理光电器件的咔唑基自组装单分子层的最新进展
Adv Mater. 2024 Aug;36(33):e2405630. doi: 10.1002/adma.202405630. Epub 2024 Jun 28.

用于高性能倒置钙钛矿太阳能电池双面埋入界面钝化的苄基膦酸工程化致密自组装单分子层

Benzylphosphonic Acid-Engineered Compact Self-Assembled Monolayers for Bifacial Buried Interface Passivation in High-Performance Inverted Perovskite Solar Cells.

作者信息

Zhang Liujiang, Fu Meirong, Jiang Xianyuan, Zhang Ziheng, Wang Chenyue, Su Zhenhuang, He Bingchen, Tang Lin, Zheng Guanhaojie, Gao Xingyu, He Jianhua

机构信息

The Institute for Advanced Studies, Wuhan University, Wuhan, 430072, China.

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201204, China.

出版信息

Adv Sci (Weinh). 2025 Dec;12(45):e12117. doi: 10.1002/advs.202512117. Epub 2025 Sep 25.

DOI:10.1002/advs.202512117
PMID:40995688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12677647/
Abstract

While [4-(3,6-Dimethyl-9H-carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) self-assembled monolayers (SAMs) enable high-performance inverted perovskite solar cells (PSCs), their sparse coverage on nickel oxide (NiOx) induces heterogeneous interfacial charge distribution at the buried perovskite interface. This increases non-radiative recombination, ultimately limiting device performance. Herein, benzylphosphonic acid (BPPA) is added, a small molecule featuring a phosphonic acid group, into Me-4PACz to construct a co-assembled monolayer (Co-SAM) with enhanced molecular ordering on NiOx. The resulting compact Co-SAM hole transport layer (HTL) simultaneously improves electrical conductivity, hole mobility, and interfacial energy level alignment, facilitating efficient hole injection. Moreover, BPPA's phosphonic acid groups enable bifacial passivation: coordinating NiOx surface defects while chelating uncoordinated Pb at the perovskite interface, significantly suppressing non-radiative recombination. Optimized Me-4PACz/BPPA-based PSCs achieve a champion power conversion efficiency (PCE) of 26.35%, while retaining 90% of the initial efficiency after 3000 h in a nitrogen atmosphere without encapsulation. This molecular co-assembly strategy concurrently refines HTL properties and buried interface passivation, providing a generalized approach for high-efficiency, stable PSCs.

摘要

虽然[4-(3,6-二甲基-9H-咔唑-9-基)丁基]膦酸(Me-4PACz)自组装单分子层(SAMs)可实现高性能倒置钙钛矿太阳能电池(PSC),但其在氧化镍(NiOx)上的稀疏覆盖会在掩埋的钙钛矿界面处引发异质界面电荷分布。这会增加非辐射复合,最终限制器件性能。在此,将具有膦酸基团的小分子苄基膦酸(BPPA)添加到Me-4PACz中,以在NiOx上构建具有增强分子有序性的共组装单分子层(Co-SAM)。由此形成的致密Co-SAM空穴传输层(HTL)同时提高了电导率、空穴迁移率和界面能级对准,促进了高效空穴注入。此外,BPPA的膦酸基团可实现双面钝化:配位NiOx表面缺陷,同时螯合钙钛矿界面处未配位的Pb,显著抑制非辐射复合。基于优化的Me-4PACz/BPPA的PSC实现了26.35%的最佳功率转换效率(PCE),并且在无封装的氮气气氛中3000小时后仍保留初始效率的90%。这种分子共组装策略同时优化了HTL性能和掩埋界面钝化,为高效、稳定的PSC提供了一种通用方法。