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Title: | New carbazole based dyes as effective co-sensitizers for DSSCs sensitized with ruthenium (II) complex (NCSU-10) |
Authors: | Naik, P. Su, R. Elmorsy, M.R. El-Shafei, A. Adhikari, A.V. |
Issue Date: | 2018 |
Citation: | Journal of Energy Chemistry, 2018, Vol.27, 2, pp.351-360 |
Abstract: | Herein, we report the design and synthesis of three new D A type metal-free carbazole based dyes (S1 3) as effective co-sensitizers for dye-sensitized solar cell (DSSC) sensitized with Ru(II) complex (NCSU-10). In this new design, the electron rich carbazole unit was attached to three different electron withdrawing/anchoring species, viz. 4-amino benzoic acid, sulfanilic acid and barbituric acid. The dyes were characterized by spectral, photophysical and electrochemical analysis. Their optical and electrochemical parameters along with molecular geometries, optimized from DFT have been employed to apprehend the effect of the structures of these co-sensitizers on the photovoltaic performances. Further, S1 3 dyes were co-sensitized along with a well-known NCSU-10 dye in order to broaden the spectral response of the co-sensitized devices and hence improve the efficiency. The photovoltaic performance studies indicated that, the device fabricated using S1 dye as co-sensitizer with 0.2 mM of NCSU-10 exhibited improved PCE of 9.55% with JSC of 22.85 mA cm?2, VOC of 0.672 V and FF of 62.2%, whereas the DSSC fabricated with dye NCSU-10 (0.2 mM) alone displayed PCE of 8.25% with JSC of 20.41 mA cm?2, VOC of 0.667 V and FF of 60.6%. Furthermore, electronic excitations simulated using time-dependent DFT, were in good agreement with the experimentally obtained results of the co-sensitizers, indicating that the exchange-correlation function and basis set utilized for predicting the spectra of the co-sensitizers are quite appropriate for the calculations. In conclusion, the results showed the potential of simple organic co-sensitizers in the development of efficient DSSCs. 2017 Science Press |
URI: | http://idr.nitk.ac.in/jspui/handle/123456789/12197 |
Appears in Collections: | 1. Journal Articles |
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