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Research Article | Open Access

Star-shaped bridge-linking polymer for robust buried interface in high-efficiency and stable perovskite solar cells

Yuetong Wu1,§Zhenxiao Lv1,§Xiangyu Li2,§Yu Zhang1Xiao Zhu3Yanrun Chen1Wenfang Zheng4Rundong Fan1Zifeng Wu1Huachao Zai3Lianghui Liu1Guangyao Cui1Xiaowei Wang2Kailin Li1Cheng Zhu4Anchao Feng2 ( )Huanping Zhou1,5,6 ( )
Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, School of Materials Science and Engineering, Peking University, Beijing 100871, China
State Key Laboratory of Organic–Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, China
School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing 100083, China
School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China
Institute of Carbon Neutrality, Peking University, Beijing 100871, China
Southwest United Graduate School, Kunming 650092, China

§ Yuetong Wu, Zhenxiao Lv, and Xiangyu Li contributed equally to this work.

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Abstract

Metal halide perovskite solar cells (PSCs) are anticipated to play a pivotal role in the next generation of photovoltaic technologies, but their unsatisfactory stability hinders further commercial applications. Particularly, numerous interfacial defects and poor mechanical adhesion at the perovskite buried interface present a critical obstacle hindering power conversion efficiency (PCE) and long-term stability of PSCs. Here, different from conventional small-molecule or linear polymer interface modifiers, we introduce a star-shaped PMMA-b-PDMAEMA (S-MD, where PMMA = poly(methyl methacrylate) and PDMAEMA = poly(dimethylaminoethyl methacrylate)) polymer as a multifunctional bridge-linking polymer for simultaneous defect passivation and mechanical reinforcement at the buried interface of inverted (p–i–n) PSCs. S-MD features a three-dimensional architecture with multiple extended conjugated arms, offering multiple Lewis base functional groups (e.g., C=O and R–N(CH3)2) with a high density of multidentate coordination sites. These groups can effectively coordinate with electron-deficient defects at the perovskite buried interface, enabling improved crystallization, reduced defect density, and enhanced interfacial adhesion. As a result, the interfacial fracture strength increases from 0.13 to 1.66 MPa. The resultant device achieves a PCE of 26.35% (certified steady-state PCE of 25.96%). The flexible device retains over 90% of its initial efficiency after 3000 flexing cycles at a curvature radius of 6 mm (R = 6 mm). This work highlights a multidentate coordinating, star-shaped polymer interface strategy that offers a promising pathway toward highly efficient and stable inverted PSCs.

Graphical Abstract

A star-shaped bridge-linking polymer (PMMA-b-PDMAEMA (S-MD, where PMMA = poly(methyl methacrylate) and PDMAEMA = poly(dimethylaminoethyl methacrylate))) is introduced to passivate defects and enhance mechanical adhesion at the buried interface of inverted perovskite solar cells (PSCs). The resultant device achieves a power conversion efficiency (PCE) of 26.35% (certified steady-state PCE of 25.96%) and the flexible device retains over 90% of its initial efficiency after 3000 flexing cycles at a curvature radius of 6 mm (R = 6 mm). This work highlights a multidentate coordinating, star-shaped polymer interface strategy that offers a promising pathway toward highly efficient and stable inverted PSCs.

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Nano Research
Article number: 94908049

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Cite this article:
Wu Y, Lv Z, Li X, et al. Star-shaped bridge-linking polymer for robust buried interface in high-efficiency and stable perovskite solar cells. Nano Research, 2026, 19(2): 94908049. https://doi.org/10.26599/NR.2025.94908049
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Received: 10 July 2025
Revised: 04 September 2025
Accepted: 08 September 2025
Published: 30 January 2026
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).