<p>Perovskite solar cells represent a promising class of photovoltaics that have achieved exceptional levels of performance within a short time. Such high efficiencies often depend on the use of molecule-based selective contacts that form highly ordered molecular assemblies. Although this high degree of ordering usually benefits charge-carrier transport, it is disrupted by structure deformation and phase transformation when subjected to external stresses, which limits the long-term operational stability of perovskite solar cells. Here we demonstrate a molecular contact with an orthogonal <i>π</i>-skeleton that shows better resilience to external stimuli than commonly used conjugated cores. This molecular design yields a disordered, amorphous structure that is not only highly stable but also demonstrates exceptional charge selectivity and transport capability. The perovskite solar cells fabricated with this orthogonal <i>π</i>-skeleton molecule exhibited enhanced long-term durability in accelerated-ageing tests. This orthogonal <i>π</i>-skeleton functionality opens new opportunities in molecular design for applications in organic electronics.</p><p></p>

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Molecular contacts with an orthogonal π-skeleton induce amorphization to enhance perovskite solar cell performance

  • Jingjing Zhou,
  • Yixin Luo,
  • Runda Li,
  • Liuwen Tian,
  • Ke Zhao,
  • Jiahui Shen,
  • Donger Jin,
  • Zixuan Peng,
  • Libing Yao,
  • Li Zhang,
  • Qingqing Liu,
  • Shaochen Zhang,
  • Lu Jin,
  • Shenglong Chu,
  • Sisi Wang,
  • Yuan Tian,
  • Jiazhe Xu,
  • Xu Zhang,
  • Pengju Shi,
  • Xiaonan Wang,
  • Wei Fan,
  • Xuechun Sun,
  • Jingyi Sun,
  • Luo-Zhou Chen,
  • Gang Wu,
  • Wen Shi,
  • Hong-Fei Wang,
  • Tianqi Deng,
  • Rui Wang,
  • Deren Yang,
  • Jingjing Xue

摘要

Perovskite solar cells represent a promising class of photovoltaics that have achieved exceptional levels of performance within a short time. Such high efficiencies often depend on the use of molecule-based selective contacts that form highly ordered molecular assemblies. Although this high degree of ordering usually benefits charge-carrier transport, it is disrupted by structure deformation and phase transformation when subjected to external stresses, which limits the long-term operational stability of perovskite solar cells. Here we demonstrate a molecular contact with an orthogonal π-skeleton that shows better resilience to external stimuli than commonly used conjugated cores. This molecular design yields a disordered, amorphous structure that is not only highly stable but also demonstrates exceptional charge selectivity and transport capability. The perovskite solar cells fabricated with this orthogonal π-skeleton molecule exhibited enhanced long-term durability in accelerated-ageing tests. This orthogonal π-skeleton functionality opens new opportunities in molecular design for applications in organic electronics.