4.7 Article

Efficient and Stable Perovskite Solar Cells by Fluorinated Ionic Liquid-Induced Component Interaction

Journal

SOLAR RRL
Volume 5, Issue 1, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/solr.202000582

Keywords

component interaction; fluorinated ionic liquids; perovskite solar cells; stability

Funding

  1. Natural Science Foundation of China [51972172, 61705102, 91833304]
  2. Natural Science Basic Research Plan in Shaanxi Province of China [2019JM-326]
  3. Joint Research Funds of Department of Science & Technology of Shaanxi Province
  4. Northwestern Polytechnical University [2020GXLH-Z-018]
  5. Young 1000 Talents Global Recruitment Program of China
  6. Fundamental Research Funds for the Central Universities
  7. TUM.solar in the context of the Bavarian Collaborative Research Project Solar Technologies Go Hybrid (SolTech)

Ask authors/readers for more resources

A novel strategy to enhance the performance and stability of organic halide perovskite solar cells by adding a small amount of the ionic liquid MA(+)DFA(-) is reported. The ionic liquid can anchor the organic cations via hydrogen bonding and improve the Pb-O interaction, leading to improved stability and superior photo carrier dynamics. Devices with high efficiency and excellent stability over 180 days in a nitrogen atmosphere at room temperature are achieved with the ionic liquid.
The instability of organic cations in lead halide perovskite materials is a major obstacle for the commercial breakthrough of perovskite photovoltaics due to desorption of organic cations during the thermal annealing and device operation. Herein, a novel strategy is reported to improve the performance and stability of organic halide perovskite solar cells containing organic cations by adding a small amount of the ionic liquid methylammonium difluoroacetate (MA(+)DFA(-)). Nuclear magnetic resonance and Fourier-transform infrared spectroscopy measurements show that MA(+)DFA(-) can anchor the organic cations via hydrogen bonding and enhance the Pb-O interaction in perovskite precursors, leading to the retardation of the perovskite crystallization and improved stability of the perovskite precursor solution. Dynamic light scattering and scanning electron microscopy verify the defect-passivation effect of MA(+)DFA(-) on the perovskite precursors and films. The passivated perovskite film shows superior photo carrier dynamics as investigated by time-resolved photoluminescence and transient absorption spectra. Moreover, the hydrogen bonding of the perovskite with MA(+)DFA(-) imparts excellent ambient and thermal stability to the film as revealed by X-ray diffraction measurements. As a result, devices with a high efficiency of 21.46% and excellent stability over 180 days in nitrogen atmosphere at room temperature are achieved with the ionic liquid.

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