4.7 Article

Chemical Stabilization of Perovskite Solar Cells with Functional Fulleropyrrolidines

Journal

ACS CENTRAL SCIENCE
Volume 4, Issue 2, Pages 216-222

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscentsci.7b00454

Keywords

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Funding

  1. Office of Naval Research, Materials Division [N00014-15-1-2244]
  2. NSF-CHE [1506839]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [1506839] Funding Source: National Science Foundation

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While perovskite solar cells have invigorated the photovoltaic research community due to their excellent power conversion efficiencies (PCEs), these devices notably suffer from poor stability. To address this crucial issue, a solution-processable organic chemical inhibition layer (OCIL) was integrated into perovskite solar cells, resulting in improved device stability and a maximum PCE of 16.3%. Photoenhanced self-doping of the fulleropyrrolidine mixture in the interlayers afforded devices that were advantageously insensitive to OCIL thickness, ranging from 4 to 190 nm. X-ray photoelectron spectroscopy (XPS) indicated that the fulleropyrrolidine mixture improved device stability by stabilizing the metal electrode and trapping ionic defects (i.e., I-) that originate from the perovskite active layer. Moreover, degraded devices were rejuvenated by repeatedly peeling away and replacing the OCIL/Ag electrode, and this repeel and replace process resulted in further improvement to device stability with minimal variation of device efficiency.

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