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Strengthened Charge-Selective Perovskite/SAM Heterocontact for Efficient and Durable Perovskite Solar Cells via Interfacial Reconfiguration

  • Xiaoyun Wan
  • , Hao Wang
  • , Haixin Chen
  • , Kai Jiang
  • , Jiyuan Chen
  • , Di Li
  • , Xuelin Wang
  • , Ziheng Zhang
  • , Zhijie Wang
  • , Menghui Jia
  • , Shuo Zhang
  • , Ruihao Tang
  • , Jinxiang Wang
  • , Lixuan Kan
  • , Zaifei Ma
  • , Bo Li
  • , Yongbo Yuan
  • , Shaobing Xiong
  • , Yefeng Yao
  • , Jianxin Tang
  • Junhao Chu, Qinye Bao*
*此作品的通讯作者
  • School of Physics
  • East China Normal University
  • College of Future Information Technology
  • Fudan University
  • Key Laboratory of Polar Materials and Devices (MOE)
  • College of Materials Science and Engineering
  • Donghua University
  • Soochow University
  • Shanghai Frontiers Science Research Base of Intelligent Optoelectronics and Perception
  • Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center
  • East China University of Science and Technology
  • Central South University
  • School of Chemistry and Chemical Engineering
  • Shanghai Jiao Tong University
  • Shanxi University

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

Hole-selective self-assembled molecular (SAM) layer plays a critical role in driving the optoelectronic performance of inverted perovskite solar cells (PSCs). Nevertheless, the inherent aggregation of SAMs at the buried heterocontact that causes large energy loss and severe instability, strongly hinders PSCs’ practical deployment. Herein, we propose an effective in situ strategy of reconfiguring a robust buried hole-selective heterocontact between SAM and perovskite to promote charge extraction with improved energetics, while suppressing the formation of interfacial voids and defects. We also demonstrate that thermally activated polymerization network densely covers the SAM at the heterocontact, minimizing underlying electrode exposure and preventing upper perovskite decomposition. Simultaneously, perovskite film directly grown on network exhibits a higher crystallinity, along with releasing the residual stress. Consequently, the PSC achieves an impressive efficiency of 26.87% for 1.57 eV bandgap cells and one of the highest fill factors of 87.04% reported so far. Encouragingly, the modified device features an excellent thermal and operational stability, significantly advancing the progress of PSCs toward industrialization.

源语言英语
期刊论文编号e1018855
期刊Angewandte Chemie - International Edition
卷65
期40
DOI
出版状态已出版 - 28 9月 2026

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