4.6 Article

Improved Absorber Phase Stability, Performance, and Lifetime in Inorganic Perovskite Solar Cells with Alkyltrimethoxysilane Strain-Release Layers at the Perovskite/TiO2 Interface

期刊

ACS ENERGY LETTERS
卷 7, 期 10, 页码 3531-3538

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.2c01610

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资金

  1. U.S. DOE Office of Science Facilities, at Brookhaven National Laboratory [DE-SC0012704]
  2. Princeton Center for Complex Materials, a National Science Foundation (NSF) -MRSEC program [DMR-1420541]
  3. Maeder Graduate Fellowship in Energy and the Environment
  4. National Science Foundation [DMR-1627453, CMMI-1824674, STTR-1843743]
  5. United States - Israel Binational Science Foundation [2018349]

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Compared to its hybrid counterparts, all-inorganic beta-CsPbI3 exhibits superior chemical and thermal stability. However, the stability of beta-CsPbI3 perovskite solar cells (PSCs) under normal operating conditions is still not as good as hybrid counterparts. A study found that lattice distortion near the perovskite/electron transport layer (ETL) interface can induce polymorphic transformation in aged CsPbI3 films. By introducing strain-release layers (SRLs) at the perovskite/ETL interface, the lattice distortion is effectively suppressed, leading to improved charge transfer and stability. Incorporating this approach in beta-CsPbI3 solar cells resulted in high efficiency and long operational lifetime under continuous illumination.
All-inorganic beta-CsPbI3 has superior chemical and thermal stability compared to its hybrid counterparts, but the stability of state-of-the-art beta-CsPbI3 perovskite solar cells (PSCs) under normal operating conditions (i.e., under illumination in an inert atmosphere) remains inferior to their hybrid counterparts. Here, we found that the lattice distortion in CsPbI3 near the perovskite/electron transport layer (ETL) interface can induce polymorphic transformation in encapsulated CsPbI3 films aged under illumination. To suppress this lattice distortion, we introduced alkyltrimethoxysilane strain-release layers (SRLs) at the perovskite/ETL interface. We found the SRL with the longest alkyl chain is the most effective at reducing interfacial lattice distortion, leading to enhanced charge transfer at the perovskite/ETL interface and improved phase/device stability. Its incorporation in beta-CsPbI3 solar cells resulted in a power-conversion efficiency of 20.1% and an operational lifetime with an extrapolated T(80 )of > 3000 h for encapsulated devices tested under continuous illumination under maximum power point tracking conditions.

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