• Opto-Electronic Science
  • Vol. 1, Issue 4, 210005 (2022)
Efthymis Serpetzoglou1、*, Ioannis Konidakis1, George Kourmoulakis1、3, Ioanna Demeridou1、4, Konstantinos Chatzimanolis2, Christos Zervos2, George Kioseoglou1、3, Emmanuel Kymakis2, and Emmanuel Stratakis1、3、4、*
Author Affiliations
  • 1Institute of Electronic Structure and Laser (IESL), Foundation for Research and Technology-Hellas (FORTH), Herakleio 70013, Greece
  • 2Electrical and Computer Engineering Department, Hellenic Mediterranean University, Herakleio 71004, Greece
  • 3Department of Materials Science and Technology, University of Crete, Herakleio 70013, Greece
  • 4Department of Physics, University of Crete, Herakleio 70013, Greece
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    DOI: 10.29026/oes.2022.210005 Cite this Article
    Efthymis Serpetzoglou, Ioannis Konidakis, George Kourmoulakis, Ioanna Demeridou, Konstantinos Chatzimanolis, Christos Zervos, George Kioseoglou, Emmanuel Kymakis, Emmanuel Stratakis. Charge carrier dynamics in different crystal phases of CH3NH3PbI3 perovskite[J]. Opto-Electronic Science, 2022, 1(4): 210005 Copy Citation Text show less
    μPL spectra following excitation at 543 nm of the (a) Glass/CH3NH3PbI3, (b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3 architectures.
    Fig. 1. μPL spectra following excitation at 543 nm of the (a) Glass/CH3NH3PbI3, (b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3 architectures.
    Shift of the μPL emission peak as a function of temperature for (a) Glass/CH3NH3PbI3,(b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3 architectures for the orthorhombic (red solid circles) and tetragonal (blue solid circles) perovskite crystal phases.
    Fig. 2. Shift of the μPL emission peak as a function of temperature for (a) Glass/CH3NH3PbI3,(b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3 architectures for the orthorhombic (red solid circles) and tetragonal (blue solid circles) perovskite crystal phases.
    FWHM of the PL peaks corresponding to the orthorhombic (black diamonds) and tetragonal (red circles) phases of CH3NH3PbI3 as a function of temperature (a) Glass/CH3NH3PbI3, (b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3. Green solid lines show the fitting acquired by the temperature-independent inhomogeneous broadening (Γ0) and the interaction between charge carriers and longitudinal optical phonons (LO-phonons), as described by the Fröhlich Hamiltonian.
    Fig. 3. FWHM of the PL peaks corresponding to the orthorhombic (black diamonds) and tetragonal (red circles) phases of CH3NH3PbI3 as a function of temperature (a) Glass/CH3NH3PbI3, (b) Glass/ITO/PEDOT:PSS/CH3NH3PbI3 and (c) Glass/ITO/PTAA/CH3NH3PbI3. Green solid lines show the fitting acquired by the temperature-independent inhomogeneous broadening (Γ0) and the interaction between charge carriers and longitudinal optical phonons (LO-phonons), as described by the Fröhlich Hamiltonian.
    Optical density (ΔOD) vs. wavelength at various delay times for Glass/ITO/PEDOT:PSS/CH3NH3PbI3 architecture at (a) 85 K, (b) 120 K and (c) 180 K.
    Fig. 4. Optical density (ΔOD) vs. wavelength at various delay times for Glass/ITO/PEDOT:PSS/CH3NH3PbI3 architecture at (a) 85 K, (b) 120 K and (c) 180 K.
    Optical density ΔOD vs. wavelength at various delay times for Glass/ITO/PTAA/CH3NH3PbI3 configuration at (a) 85 K, (b) 120 K and (c) 180 K.
    Fig. 5. Optical density ΔOD vs. wavelength at various delay times for Glass/ITO/PTAA/CH3NH3PbI3 configuration at (a) 85 K, (b) 120 K and (c) 180 K.
    Optical density (ΔOD) peaks wavelength as a function of temperature for Glass/ITO/PEDOT:PSS/CH3NH3PbI3 architecture and Glass/ITO/PTAA/CH3NH3PbI3configurations, as extracted from TAS spectra at t = 0 ps (see Fig. 4 and Fig. 5 blue lines).
    Fig. 6. Optical density (ΔOD) peaks wavelength as a function of temperature for Glass/ITO/PEDOT:PSS/CH3NH3PbI3 architecture and Glass/ITO/PTAA/CH3NH3PbI3configurations, as extracted from TAS spectra at t = 0 ps (see Fig. 4 and Fig. 5 blue lines).
    Normalized optical density (ΔOD) vs. delay time for Glass/ITO/PEDOT:PSS/CH3NH3PbI3and Glass/ITO/PTAA/CH3NH3PbI3configurations for the orthorhombic phase at (a) 85 K, (b) 120 K and for the tetragonal phase at (c) 120 K and (d) 180 K. Symbols present the transient band edge bleach kinetics, while solid lined present the decay exponential fitting. Insets are shown the initial time scale for Glass/ITO/PTAA/CH3NH3PbI3.
    Fig. 7. Normalized optical density (ΔOD) vs. delay time for Glass/ITO/PEDOT:PSS/CH3NH3PbI3and Glass/ITO/PTAA/CH3NH3PbI3configurations for the orthorhombic phase at (a) 85 K, (b) 120 K and for the tetragonal phase at (c) 120 K and (d) 180 K. Symbols present the transient band edge bleach kinetics, while solid lined present the decay exponential fitting. Insets are shown the initial time scale for Glass/ITO/PTAA/CH3NH3PbI3.
    Temperature (K) PEDOT: PSSPTAA
    λmax (nm) τ1 ± 2 (ps) τ2 ± 8 (ps) τ3 ± 13 (ps) k2±0.2×10–10 (cm3s–1) λmax (nm) τ1 ± 2 (ps) τ2 ± 8 (ps) τ3 ± 13 (ps) k2±0.2×10–10 (cm3s–1)
    857376.15625629.9×10–107276.22962969.1×10–10
    120730121719629.9×10–107245.7643243.8×10–10
    76616.74499951.3×10–97607.31373626.6×10–10
    18075214.72669331.2×10–107665.75718391.0×10–10
    Table 1. Time components and bimolecular recombination rate (k2) for the Glass/ITO/PEDOT:PSS/CΗ33PbΙ3 and Glass/ITO/PTAA/CH3NH3PbI3 architectures.
    Efthymis Serpetzoglou, Ioannis Konidakis, George Kourmoulakis, Ioanna Demeridou, Konstantinos Chatzimanolis, Christos Zervos, George Kioseoglou, Emmanuel Kymakis, Emmanuel Stratakis. Charge carrier dynamics in different crystal phases of CH3NH3PbI3 perovskite[J]. Opto-Electronic Science, 2022, 1(4): 210005
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