4.8 Article

Constructing All-Inorganic Perovskite/Fluoride Nanocomposites for Efficient and Ultra-Stable Perovskite Solar Cells

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 47, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202106386

Keywords

CsPbI; (3); F-passivation; perovskite solar cells; photoluminescence; stability

Funding

  1. Strategic Priority Research Program of CAS [XDB20000000]
  2. Director's Fund of Fujian Science & Technology Innovation Laboratory for Optoelectronic Information [2020ZZ114]
  3. National Natural Science Foundation of China (NSFC) [21731006, 91733301, 51872007, 21871256]
  4. Key Research Program of Frontier Sciences CAS [QYZDY-SSW-SLH025]
  5. National Key Research and Development Program of China [2019YFA0707003, 2019YFE0114100]

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Organic-inorganic hybrid perovskite solar cells have faced challenges in achieving both high efficiency and long-term stability. A new CsPbI3/CaF2 perovskite/fluoride nanocomposite shows promise in addressing these issues, delivering efficient and ultra-stable performance. By incorporating CaF2 into the crystal lattice of CsPbI3 perovskite, the nanocomposite effectively passivates defects and suppresses ion migration, resulting in improved power conversion efficiency and extended device lifetime compared to control devices.
Organic-inorganic hybrid perovskite solar cells (PSCs) have rapidly developed over the past decade and have achieved the latest certified power conversion efficiency (PCE) up to 25.5%. However, unsatisfactory long-term operational stability for these hybrid PSCs remains a huge obstacle to further development and commercialization. Herein, a unique hetero-structured CsPbI3/CaF2 perovskite/fluoride nanocomposites (PFNCs) is fabricated via a newly developed facile two-step hetero-epitaxial growth strategy to deliver efficient and ultra-stable PSCs. After being incorporated into the crystal lattice of alpha-phase CsPbI3 perovskite, the cubic-phase CaF2 in the resultant CsPbI3/CaF2 PFNCs can not only passivate the intrinsic defects of CsPbI3 perovskite itself but also effectively suppress the notorious ion migration in hybrid perovskite Cs(0.05)FA(0.81)MA(0.14)PbI(2.55)Br(0.45) (CsFAMA) thin-films of PSCs. As such, the CsFAMA PSC devices based on CsPbI3/CaF2-deposited perovskite thin-film achieve a mean PCE of 20.45%, in sharp contrast to 19.33% of the control devices without deposition. Specifically, the CsPbI3/CaF2-deposited PSC retains 85% of its original PCE after 1000 h continuous operation at the maximum power point under AM 1.5G solar light, far better than those of the control and CsPbI3-deposited PSCs with a device T-85 lifetime of 315 and 125 h, respectively.

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