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<p>Triple‐junction solar cells theoretically outperform their double-junction and single‐junction counterparts in power conversion efficiency, yet practical perovskite–perovskite–silicon devices have fallen short of both theoretical limits and commercial targets. To address surface defects in the top perovskite junction, we introduce a piperazine-1,4-diium chloride treatment, which replaces less stable lithium fluoride. For interfacing the top and middle perovskite junctions, we optimize the size of gold nanoparticles deposited on atomic layer-deposited tin oxide for best ohmic contacting with minimal optical losses. Applying these strategies, our champion 1-cm<sup>2</sup> triple‐junction cell achieved a third party-verified reverse‐scan power conversion efficiency of 27.06% with an open circuit voltage of 3.16 V. Scaling up to 16 cm<sup>2</sup>, the device produced a certified steady‐state power conversion efficiency of 23.3%. Device longevity also improved by eliminating methylammonium and incorporating rubidium into the perovskite bulk alongside the piperazine-1,4-diium chloride surface layer. An encapsulated 1-cm<sup>2</sup> cell retained 95% of its initial efficiency after 407 h at maximum power point and passed the IEC 61215 thermal cycling test. These results represent advancements towards efficient and stable perovskite–perovskite–silicon triple-junction solar cells.</p>

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Tailoring nanoscale interfaces for perovskite–perovskite–silicon triple-junction solar cells

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月7日

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  • Jianghui Zheng,
  • Guoliang Wang,
  • Leiping Duan,
  • Weiyuan Duan,
  • Yang Jiang,
  • Phoebe Pearce,
  • Yijun Gao,
  • Md Arafat Mahmud,
  • Chwenhaw Liao,
  • Tik Lun Leung,
  • Jueming Bing,
  • Zhuofeng Li,
  • Zhenyu Sun,
  • Xin Cui,
  • Christopher Bailey,
  • Marko Jankovec,
  • Jianpeng Yi,
  • Runmin Tao,
  • Lijie Zheng,
  • Baihong Zhu,
  • Yue Sun,
  • Nan Sun,
  • Gaosheng Huang,
  • Li Wang,
  • Andreas Lambertz,
  • Stephen Bremner,
  • Xinqin Liao,
  • Tingzhu Wu,
  • Guohua Xie,
  • Mathias Uller Rothmann,
  • Marko Topič,
  • David R. McKenzie,
  • Kaining Ding,
  • Wei Li,
  • Zhong Chen,
  • Anita W. Y. Ho-Baillie

摘要

Triple‐junction solar cells theoretically outperform their double-junction and single‐junction counterparts in power conversion efficiency, yet practical perovskite–perovskite–silicon devices have fallen short of both theoretical limits and commercial targets. To address surface defects in the top perovskite junction, we introduce a piperazine-1,4-diium chloride treatment, which replaces less stable lithium fluoride. For interfacing the top and middle perovskite junctions, we optimize the size of gold nanoparticles deposited on atomic layer-deposited tin oxide for best ohmic contacting with minimal optical losses. Applying these strategies, our champion 1-cm2 triple‐junction cell achieved a third party-verified reverse‐scan power conversion efficiency of 27.06% with an open circuit voltage of 3.16 V. Scaling up to 16 cm2, the device produced a certified steady‐state power conversion efficiency of 23.3%. Device longevity also improved by eliminating methylammonium and incorporating rubidium into the perovskite bulk alongside the piperazine-1,4-diium chloride surface layer. An encapsulated 1-cm2 cell retained 95% of its initial efficiency after 407 h at maximum power point and passed the IEC 61215 thermal cycling test. These results represent advancements towards efficient and stable perovskite–perovskite–silicon triple-junction solar cells.