4.8 Article

Guanidinium thiocyanate selective Ostwald ripening induced large grain for high performance perovskite solar cells

Journal

NANO ENERGY
Volume 41, Issue -, Pages 476-487

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2017.10.006

Keywords

Perovskite solar cells; Large grains; Improved fill factor; High efficiency; Ostwald ripening

Funding

  1. Australian Research Council Future Fellowship [FT120100674]
  2. Queensland-Chinese Academy of Science (Q-CAS) collaborative research fund
  3. Queensland University of Technology (QUT) postgraduate scholarship
  4. CSIRO top-up scholarship
  5. Science and Engineering faculty, QUT
  6. MINECO of Spain [MAT2013-47192-C3-1-R]
  7. Generalitat Valenciana [ACOMP/2015/105]
  8. Spanish Ministerio de Economia y Competitividad [RYC-2014-16809]

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Organic-inorganic lead halide perovskite has become one of the most attractive materials for future low-cost high-efficiency solar technology. However, the polycrystalline nature of perovskite thin-film often possesses an exceptional density of defects, especially at grain boundaries (GBs) and film surface, limiting further improvement in the power conversion efficiency (PCE) of the perovskite device. Here, we report a simple method to reduce GBs and to passivate the surface of a methylammonium lead tri-iodide (MAPbI(3)) film by guanidinium thiocyanate (GUTS)-assisted Ostwald ripening post treatment. High-optoelectronic quality MAPbI(3) film consisting of micron-sized grains were synthesized by post-treating a MAPbI(3) film with GUTS/isopropanol solution (4 mg/mL, GUTS-4). Analysis of the electrochemical impedance spectra (EIS) of the solar cells showed that interfacial charge recombination resistance of the device based on a GUTS-4 post-treated MAPbI(3) absorber film was increased by a factor of 1.15-2.6, depending on light illumination intensity, compared to the control MAPbI3 cell. This is consistent with results of the open-circuit voltage (V-oc) decay and the light intensity dependent photovoltage evolution which shows device with GUTS treatment had one order longer charge carrier lifetime and was more ideal (ideality factor = 1.25). Further characterization by Kelvin probe force microscope indicated that GUTS-4 treatment shifted the energetics of the MAPbI3 film by similar to 100 meV towards better energy level alignment with adjacent SnO2 electron transport layer, leading to a more favorable charge extraction process at the MAPbI(3)/SnO2 interface. As a result, the PCE of PSCs was enhanced from 14.59% to 16.37% and the hysteresis effect was mitigated.

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