4.6 Article

Multisource Vacuum Deposition of Methylammonium-Free Perovskite Solar Cells

Journal

ACS ENERGY LETTERS
Volume 5, Issue 8, Pages 2498-2504

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.0c00839

Keywords

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Funding

  1. European Research Council (ERC) [756962]
  2. Marie Sklodowska-Curie actions under the European Union's Horizon 2020 research and innovation programme [841386]
  3. Royal Society
  4. Tata Group [UF150033]
  5. Taiwan Cambridge Scholarship
  6. Henry Royce Institute, Cambridge [EP/P024947/1]
  7. Engineering and Physical Research Council (EPSRC) [EP/R023980/1]
  8. EPSRC Centre for Advanced Materials for Integrated Energy Systems (CAM-IES) [EP/P007767/1]
  9. EPSRC [EP/P007767/1, EP/R023980/1, EP/P024947/1, EP/S019367/1] Funding Source: UKRI
  10. Marie Curie Actions (MSCA) [841386] Funding Source: Marie Curie Actions (MSCA)

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Halide perovskites of the form ABX(3) have shown outstanding properties for solar cells. The highest reported compositions consist of mixtures of A-site cations methylammonium (MA), formamidinium (FA) and cesium, and X-site iodide and bromide ions, and are produced by solution processing. However, it is unclear whether solution processing will yield sufficient spatial performance uniformity for large-scale photovoltaic modules or compatibility with deposition of multilayered tandem solar cell stacks. In addition, the volatile MA cation presents long-term stability issues. Here, we report the multisource vacuum deposition of FA(0.7)Cs(0.3)Pb(I0.9Br0.1)(3) perovskite thin films with high-quality morphological, structural, and optoelectronic properties. We find that the controlled addition of excess PbI2 during the deposition is critical for achieving high performance and stability of the absorber material, and we fabricate p-i-n solar cells with stabilized power output of 18.2%. We also reveal the sensitivity of the deposition process to a range of parameters, including substrate, annealing temperature, evaporation rates, and source purity, providing a guide for further evaporation efforts. Our results demonstrate the enormous promise for MA-free perovskite solar cells employing industry-scalable multisource evaporation processes.

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