4.6 Article

Passivated perovskite crystallization and stability in organic-inorganic halide solar cells by doping a donor polymer

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 5, Issue 6, Pages 2572-2579

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ta08970d

Keywords

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Funding

  1. National Natural Science Foundation of China [61540016, 61674109, 11605278, 11675252]
  2. China Postdoctoral Science Foundation [2015M580460]
  3. Collaborative Innovation Center of Suzhou Nano Science and Technology (Nano-CIC)
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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Photovoltaic performance of planar perovskite hybrid solar cells (pero-HSCs) has been improved by mixing CH(3)NH(3)PbIxCl(3-x) and an electron donor polymer [ N-9''-hepta-hecanyl- 2,7-carbazole-alt- 5,5-(4',7'-di-2-thienyl- 2',1',3'-benzothiadiaz-ole)] (PCDTBT). PCDTBT contains lone pairs of electrons due to the presence of S and N atoms, which could passivate the trap states of the perovskite layer and thus reduce the number of film defects. A Stonehenge-like structure could be formed by the interaction of CH(3)NH(3)PbIxCl(3-x) and PCDTBT, developing more ordered orientation crystallization and a high quality film morphology. The doped solar cells are characterized by their excellent photovoltaic properties and enhanced stability. When the doping concentration is 0.3 mg mL(-1), the fabricated solar cell device exhibits an outstanding power conversion efficiency (PCE) of 15.76%, which represents a significant improvement with respect to the magnitude of 16% obtained for the reference device.

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