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Buried interface anchoring with silane coupling agents for low voltage loss and high-efficiency wide-bandgap perovskite solar cells

  • Ting Zhang
  • , Rudai Zhao
  • , Pengwei Li
  • , Peiwen Gu
  • , Yapeng Shi
  • , Shuaishuai Li
  • , Zhipeng Miao
  • , Sihui Peng
  • , Yunhang Xie
  • , Wenlong Liang
  • , Jie Yu
  • , Chao Liang
  • , Yiqiang Zhang
  • , Yanlin Song
  • Zhengzhou University
  • Chinese Academy of Sciences

科研成果: 期刊稿件文章同行评审

6 引用 (Scopus)

摘要

Perovskite tandem solar cells (TSCs) hold substantial promise for surpassing the efficiency limits of single-junction solar cells. Nevertheless, achieving high open-circuit voltage (VOC) in wide-bandgap perovskite devices remains a challenge due to significant VOC-losses. Here, we introduce a heterogeneous interface anchoring strategy aimed at enhancing interfacial properties by incorporating a silane coupling agent between the perovskite and hole transport layers. Trimethoxysilane (TMOS), an amphiphilic molecule, strengthens interfacial adhesion through enhanced chemical interactions, thereby promoting efficient hole extraction. Additionally, the terminal functional groups of TMOS molecules interact with lead ions, modulating the perovskite film crystallization and improving their overall quality. Devices treated with TMOS exhibit a marked reduction in non-radiative recombination, leading to a significant increase in VOC. Notably, 3-cyanopropyltrimethoxysilane (CN-TMOS) optimizes the uniformity and interfacial contact of the perovskite film, achieving a VOC of 1.345 V and a power conversion efficiency (PCE) of 19.69%. The corresponding VOC-loss, relative to the bandgap, is reduced to 0.425 V, one of the lowest values reported for wide-bandgap perovskite single-junction solar cells. Extending this strategy to all-perovskite TSCs, we achieve a PCE of 28.45% and exceptional operational stability, retaining over 90% of the initial efficiency after 500 h of continuous operation under 1 sun illumination.

源语言英语
页(从-至)3571-3579
页数9
期刊Science Bulletin
70
21
DOI
出版状态已出版 - 15 11月 2025

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