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Strong Coupling of NiOx and Self-Assembled Molecules via Inserted Reductant for High-Performance Inverted Perovskite Solar Cells

  • Hui Chen
  • , Qi Cao
  • , Xingyu Pu
  • , Qingyuan Zhao
  • , Xilai He
  • , Zihao Zhou
  • , Tong Wang
  • , Guangpeng Feng
  • , Ranhao Yin
  • , Zhongwei Chen
  • , Ilkhom Tajibaev
  • , Ilkhom Boynazarov
  • , Yijun Bai
  • , Shiyao Jia
  • , Xuanhua Li
  • Northwestern Polytechnical University Xian
  • College of Physics
  • Academy of Sciences of the Republic of Uzbekistan
  • Tashkent State Technical University

科研成果: 期刊稿件文章同行评审

18 引用 (Scopus)

摘要

Self-assembled molecules (SAMs) deposited on nickel oxide (NiOx) are the basis for achieving high-performance inverted perovskite solar cells (PSCs). Unfortunately, the dissolution and redeposition of SAMs caused by the perovskite precursors leads to leaky monolayers, resulting in perovskite degradation and reduced stability. Here, a novel method is reported to realize strong coupling between NiOx and SAMs via inserted reductant [9tris(2-carboxyethyl)phosphine hydrochloride (TCEP)] for an integrated NiOx-SAMs hole transport layer (HTL). TCEP reduces NiOx and in situ forms C═O···Ni coordinated bond and O─H···O─Ni hydrogen bond, while its -COOH is connected with SAM's -PO(OH)2 by phosphonate and hydrogen bond, which improve the compactness of SAMs, thereby strengthening hole extraction and lowering interfacial non-radiative recombination. Simulation calculations demonstrate that the HTL strongly coupled by TCEP has a stronger adsorption energy, significantly improving device long-term stability. Therefore, the device based on integrated NiOx-SAMs HTL obtains a substantial efficiency of 26.34%. The devices maintain an impressive 97.5% of their original efficiency after 1000 h of operation under 1-sun illumination and 90.1% after 1000 h of thermal treatment at 85 °C in nitrogen atmosphere. This work offers new horizons for designing NiOx-based HTLs with high SAMs coverage for high-performance PSCs.

源语言英语
文章编号e10553
期刊Advanced Materials
37
43
DOI
出版状态已出版 - 29 10月 2025

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