4.8 Article

Light-Induced Increase of Electron Diffusion Length in a p-n Junction Type CH3NH3PbBr3 Perovskite Solar Cell

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 6, Issue 13, Pages 2469-2476

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.5b00889

Keywords

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Funding

  1. Leona M. and Harry B. Helmsley Charitable Trust
  2. Israel National Nano-Initiative
  3. Israel Ministry of Science
  4. Nancy and Stephen Grand Center for Sensors and Security
  5. Helmholtz Virtual Institute Microstructure Control in Thin-Film Solar Cells [VI-520]
  6. WIS for an Alternative Sustainable Energy Initiative (AERI)

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High band gap, high open-circuit voltage solar cells with methylammonium lead tribromide (MAPbBr(3)) perovskite absorbers are of interest for spectral splitting and photoelectrochemical applications, because of their good performance and ease of processing. The physical origin of high performance in these and similar perovskite-based devices remains only partially understood. Using cross-sectional electron-beam-induced current (EBIC) measurements, we find an increase in carrier diffusion length in MAPbBr(3)(Cl)-based solar cells upon low intensity (a few percent of 1 sun intensity) blue laser illumination. Comparing dark and illuminated conditions, the minority carrier (electron) diffusion length increases about 3.5 times from L-n = 100 +/- 50 nm to 360 +/- 22 nm. The EBIC cross section profile indicates a p-n structure between the n-FTO/TiO, and p-perovskite, rather than the p-i-n structure, reported for the iodide derivative. On the basis of the variation in space-charge region width with varying bias, measured by EBIC and capacitance-voltage measurements, we estimate the net-doping concentration in MAPbBr(3)(Cl) to be 3-6 x 10(17) cm(-3).

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