<p>The development of molecule-based selective contacts has boosted the power conversion efficiencies of inverted perovskite solar cells. However, these molecular films, often assembled as monolayer or multiple layers on the substrate, are prone to molecular desorption and structural deformation, limiting the long-term stability of devices. This instability, in essence, originates from the weak contacting structure between the transparent conductive oxide and molecular layer, with a limited interface offering insufficient adhering forces to immobilize the molecules. A general architectural strategy that circumvents this fundamental limitation without compromising electronic functionality is highly demanded, but remains underexplored. We now report a universal architecture of a bulk nano-heterointerface that reconstructed the molecule-based selective layer. The substantially increased chemical interface and strengthened binding force between the molecules and rationally designed nanoscale scaffolds greatly improved the device operational stability, achieving high efficiency. The strategy proved versatile, successfully applied to various molecular systems to enhance device performances, and remained effective in upscaled devices produced via scalable blade coating.</p>

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Bulk nano-heterointerface secures molecular contacts in perovskite solar cells

  • Yixin Luo,
  • Jiahui Shen,
  • Ke Zhao,
  • Shenglong Chu,
  • Yuan Tian,
  • Lu Jin,
  • Caner Değer,
  • Bo-jun Zhao,
  • Xuechun Sun,
  • Libing Yao,
  • Xiaohe Miao,
  • Li Zhang,
  • Qingqing Liu,
  • Seung-Gu Choi,
  • Qinggui Li,
  • Runda Li,
  • Hengyu Zhang,
  • Haimeng Xin,
  • Jiazhe Xu,
  • Jingjing Zhou,
  • Donger Jin,
  • Rui Wang,
  • Jin-Wook Lee,
  • Ruzhang Liu,
  • Ilhan Yavuz,
  • Hong-fei Wang,
  • Hyo Jae Yoon,
  • Zhenyi Ni,
  • Deren Yang,
  • Jingjing Xue

摘要

The development of molecule-based selective contacts has boosted the power conversion efficiencies of inverted perovskite solar cells. However, these molecular films, often assembled as monolayer or multiple layers on the substrate, are prone to molecular desorption and structural deformation, limiting the long-term stability of devices. This instability, in essence, originates from the weak contacting structure between the transparent conductive oxide and molecular layer, with a limited interface offering insufficient adhering forces to immobilize the molecules. A general architectural strategy that circumvents this fundamental limitation without compromising electronic functionality is highly demanded, but remains underexplored. We now report a universal architecture of a bulk nano-heterointerface that reconstructed the molecule-based selective layer. The substantially increased chemical interface and strengthened binding force between the molecules and rationally designed nanoscale scaffolds greatly improved the device operational stability, achieving high efficiency. The strategy proved versatile, successfully applied to various molecular systems to enhance device performances, and remained effective in upscaled devices produced via scalable blade coating.