A Novel Multiple-Ring Aromatic Spacer Based 2D Ruddlesden–Popper CsPbI3 Solar Cell with Record Efficiency Beyond 16%

Huanhuan Yao, Zhizai Li, Chang Shi, Youkui Xu, Qian Wang, Zhen Hua Li, Guoqiang Peng, Yutian Lei, Haoxu Wang, More Authors

Research output: Contribution to journalArticleScientificpeer-review

10 Citations (Scopus)
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Two-dimensional (2D) Ruddlesden–Popper (RP) CsPbI3 perovskite possesses superior phase stability by introducing steric hindrance. However, due to the quantum and dielectric confinement effect, 2D structures usually exhibit large exciton binding energy, and the charge tunneling barrier across the organic interlayer is difficult to eliminate, resulting in poor charge transport and performance. Here, a multiple-ring aromatic ammonium, 1-naphthylamine (1-NA) spacer is developed for 2D RP CsPbI3 perovskite solar cell (PSC). Theoretical simulations and experimental characterizations demonstrate that the 2D RP CsPbI3 perovskite using 1-NA spacer with extended π-conjugation lengths reduces the exciton binding energy and facilitates the efficient separation of excitons. In addition, its cations have a significant contribution to the conduction band, which can reduce the bandgap, promote electronic coupling between organic and inorganic layers, and improve interlayer charge transport. Importantly, the strong π–π conjugation of 1-NA spacer can enhance intermolecular interactions and hydrogen bonding, and prepare high-quality films with preferred vertical orientation, resulting in lower defect density, and directional charge transport. As a result, the (1-NA)2(Cs)3Pb4I13 PSC exhibits a record 16.62% performance with enhanced stability. This work provides an efficient approach to improve charge transport and device performance by developing multiple-ring aromatic spacers.

Original languageEnglish
Article number2205029
Number of pages10
JournalAdvanced Functional Materials
Issue number35
Publication statusPublished - 2022

Bibliographical note

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  • charge transport
  • exciton binding energy
  • Extended π-conjugation lengths
  • vertical orientations


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