Electron-enriched thione enables strong Pb–S interaction for stabilizing high quality CsPbI 3 perovskite films with low-temperature processing

Cesium lead iodide (CsPbI 3 ) perovskite is a promising photovoltaic material with a suitable bandgap and high thermal stability. However, it involves complicated phase transitions, and black-phase CsPbI 3 is mostly formed and stabilized at high temperatures (200–360 °C), making its practical applic...

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Veröffentlicht in:Chemical science (Cambridge) 2020-03, Vol.11 (12), p.3132-3140
Hauptverfasser: Xu, Xiaojia, Zhang, Hao, Li, Erpeng, Ru, Pengbin, Chen, Han, Chen, Zhenhua, Wu, Yongzhen, Tian, He, Zhu, Wei-Hong
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Sprache:eng
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Zusammenfassung:Cesium lead iodide (CsPbI 3 ) perovskite is a promising photovoltaic material with a suitable bandgap and high thermal stability. However, it involves complicated phase transitions, and black-phase CsPbI 3 is mostly formed and stabilized at high temperatures (200–360 °C), making its practical application challenging. Here, for the first time, we have demonstrated a feasible route for growing high quality black-phase CsPbI 3 thin films under mild conditions by using a neutral molecular additive of 4(1 H )-pyridinethione (4-PT). The resulting CsPbI 3 thin films are morphologically uniform and phase stable under ambient conditions, consisting of micron-sized grains with oriented crystal stacking. With a range of characterization experiments on intermolecular interactions, the electron-enriched thione group in 4-PT is distinguished to be critical to enabling a strong Pb–S interaction, which not only influences the crystallization paths, but also stabilizes the black-phase CsPbI 3 via crystal surface functionalization. The 4-PT based CsPbI 3 achieves 13.88% power conversion efficiency in a p–i–n structured device architecture, and encapsulated devices can retain over 85% of their initial efficiencies after 20 days of storage in an ambient environment, which are the best results among fully low-temperature processed CsPbI 3 photovoltaics.
ISSN:2041-6520
2041-6539
DOI:10.1039/C9SC06574A