Natural chlorophyll-related porphyrins and chlorins for dye-sensitized solar cells

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Abstract

Natural-chlorophyll-related porphyrins, including (2H, Zn, Cu)-protoporphyrin IX (Por-1) and Zn-mesoporphyrin IX (Por-2), and chlorins, including chlorin e6 (Chl-1), chlorin e4 (Chl-2), and rhodin G7 (Chl-3), have been used in dye-sensitized solar cells (DSSCs). For porphyrin sensitizers that have vinyl groups at the β-positions, zinc coordinated Por-1 gives the highest solar-energy-to- electricity conversion efficiency (ν) of up to 2.9%. Replacing the vinyl groups of ZnPor-1 with ethyl groups increases the open-circuit voltage (V oc) from 0.61 V to 0.66 V, but decreases the short-circuit current (Jsc) from 7.0 mA·cm-2 to 6.1 mA·cm-2 and the value of ν to 2.8%. Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations suggest that the higher Jsc values of Zn-based porphyrin sensitizers result from the favorable electron injection from the LUMO at higher energy levels. In the case of the chlorin sensitizers, the number of carboxyl protons has a large effect on the photovoltaic performance. Chl-2 with two carboxyl protons gives much higher values of Jsc, Voc, and ν than does Chl-1 with three carboxyl protons. Replacing the protons of Chl-1 with sodium ions can substantially improve the photovoltaic performance of Chl-1-based solar cells. Furthermore, the sodium salt of Chl-3 with an aldehyde group at the C7 position shows poorer photovoltaic performance than does the sodium salt of Chl-1 with methyl groups at the C7 position. This is due to the low light-harvesting capability of Chl-3. © 2012 by the authors.

Figures

  • Figure 1. The chemical structures of chlorophyll related porphyrin sensitizers.
  • Figure 2. The electronic absorption spectra of porphyrin sensitizers in ethanol solution.
  • Figure 3. Calculated electronic absorption spectra for the set of porphyrin sensitizers.
  • Figure 4. Frontier molecular orbitals of the porphyrin sensitizers based on DFT/CAM-B3LYP/6-31G (d,p) calculations with CPCM (ethanol).
  • Figure 5. Comparison of energy levels of the HOMO-1, HOMO, LUMO, and LUMO molecular orbitals of the porphyrin sensitizers to that of the CBE of TiO2.
  • Figure 6. IPCE profiles and I-V curves of DSSCs based on porphyrin sensitized TiO2 electrodes.
  • Table 1. Photovoltaic performance of DSSCs using chlorophyll derivatives having porphyrin macrocycle.
  • Figure 7. The chemical structures of chlorophyll related chlorin sensitizers.

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APA

Wang, X. F., & Kitao, O. (2012). Natural chlorophyll-related porphyrins and chlorins for dye-sensitized solar cells. Molecules, 17(4), 4484–4497. https://doi.org/10.3390/molecules17044484

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