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<p>The development of efficient inverted perovskite solar cells has been propelled by the adoption of self-assembled monolayers as hole-selective contacts. Nevertheless, the durability of such devices is still hampered by the vulnerability of conventional carbazole molecules to ultraviolet (UV) damage and thermal instability of phosphonic acid anchors. Through spacer-group engineering in the benchmark molecule MeO-2PACz, we elucidated two distinct degradation pathways, with photodegradation occurring in non-conjugated linkages and thermal degradation in conjugated structures. These insights enabled rational design of a novel molecule MP3, which integrates both conjugated and non-conjugated spacer motifs with an electron-withdrawing substituent. This redesigned structure suppressed UV-induced <i>N</i>-dealkylation and thermally driven anhydride formation while enhancing substrate binding via modulated acid dissociation. MP3-based perovskite solar cells achieved a certified efficiency of 27.1% and showed exceptional stability: retaining 93.2% of their initial efficiency after 1,000 h of UV exposure, 91.1% after 100 °C thermal ageing (1,000 h) and 94.8% after 2,200 h of maximum power point tracking at 65 °C.</p>

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UV and thermally stable hole-selective contacts with enhanced assembly density for inverted perovskite solar cells

  • 期刊论文

  • 发表日期：

    2026年6月1日

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  • Liqing Zhan,
  • Zehui Sun,
  • Shuo Zhang,
  • Jingwen He,
  • Weiqun Gao,
  • Tianyin Miao,
  • Zonghao Liu,
  • Ying Zhou,
  • Leyuan Zhang,
  • Lihui Zhou,
  • Xiaofeng Chen,
  • Wei Chen,
  • Weizhong Zheng,
  • Wei Ma,
  • Martin Stolterfoht,
  • Wei-Hong Zhu,
  • Yongzhen Wu

摘要

The development of efficient inverted perovskite solar cells has been propelled by the adoption of self-assembled monolayers as hole-selective contacts. Nevertheless, the durability of such devices is still hampered by the vulnerability of conventional carbazole molecules to ultraviolet (UV) damage and thermal instability of phosphonic acid anchors. Through spacer-group engineering in the benchmark molecule MeO-2PACz, we elucidated two distinct degradation pathways, with photodegradation occurring in non-conjugated linkages and thermal degradation in conjugated structures. These insights enabled rational design of a novel molecule MP3, which integrates both conjugated and non-conjugated spacer motifs with an electron-withdrawing substituent. This redesigned structure suppressed UV-induced N-dealkylation and thermally driven anhydride formation while enhancing substrate binding via modulated acid dissociation. MP3-based perovskite solar cells achieved a certified efficiency of 27.1% and showed exceptional stability: retaining 93.2% of their initial efficiency after 1,000 h of UV exposure, 91.1% after 100 °C thermal ageing (1,000 h) and 94.8% after 2,200 h of maximum power point tracking at 65 °C.