4.8 Article

Defect Healing in FAPb(I1-xBrx)(3) Perovskites: Multifunctional Fluorinated Sulfonate Surfactant Anchoring Enables >21% Modules with Improved Operation Stability

Journal

ADVANCED ENERGY MATERIALS
Volume 12, Issue 20, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202200632

Keywords

crystallization orientation modulation; defect passivation; fluorinated sulfonate surfactants; long-term stability; perovskite solar cells

Funding

  1. Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Korea government (MOTIE) [20203040010320]
  2. Institute of Information & Communications Technology Planning & Evaluation (IITP) - Korea government [2020-0-00541]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) - Korea government [20016588]
  4. National Research Foundation of Korea (NRF) - Ministry of education [NRF-2021R1I1A1A01050938]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [20016588] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Formamidinium lead triiodide-based perovskite solar cells have shown great potential for future photovoltaic technologies. The introduction of heptadecafluorooctanesulfonic acid tetraethylammonium salt (HFSTT) as a modifier has improved the quality and stability of the perovskite films, leading to high power conversion efficiencies and long-term performance.
Formamidinium lead triiodide-based perovskite solar cells have emerged as one of the most promising candidates that can be potentially used to develop photovoltaic technologies in the future. The commercial use of perovskite solar cell modules (PSCMs) is limited as it is challenging to fabricate high-quality, efficient, and stable large-area perovskite light-absorbing films. Heptadecafluorooctanesulfonic acid tetraethylammonium salt (HFSTT), containing fluorinated long alkyl chains as hydrophobic tails and sulfonic acid groups (SO3(-)) as hydrophilic heads, which exhibit a great synergistic potential in large-area film uniform fabrication, crystallization orientation modulation, defect passivation, and device operation stability enhancement, are introduced. The HFSTT-modified films exhibit a prominent (100) orientation and lower trap-state density as well as enhanced carrier mobilities and diffusion lengths, facilitating a champion unit device with an impressive power conversion efficiency (PCE) of 23.88% (0.14 cm(2)) and 22.52% (1 cm(2)) with a low voltage deficit around 0.341 V. The unencapsulated device retains approximate to 70% of its initial efficiency after 1000 h under heat damping test (60 degrees C and approximate to 60% RH). Moreover, the PSCMs exhibiting PCEs of 21.05% (with notable fill factor 0.79) and 18.27% are characterized by the active areas of 25.98 and 60.68 cm(2), respectively.

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