Abstract
In this work, the molecular engineering approach was applied to the organic dyes of AE, AQ, TE, and TQ having the donor-acceptor (D-A) configuration to investigate the solar cell efficiency. In these structures, dimethylaniline and triphenylamine were used as the electron donors and 1,1,4,4-tetracyanobuta-1,3-dienes (originating from TCNE) and 2-(4-(4,4-dicyanobut-3-en-2-ylidene)cyclohexa-2,5-dien-1-ylidene)malononitrile (originating from TCNQ) as the electron acceptors. The incorporation of tetracyanoethylene (TCNE) and 7,7,8,8-tetracyanoquinodimethane (TCNQ) due to the strong electron-withdrawing ability enhance the performance of the dye-sensitized solar cell (DSSC). The results reveal that a change in the electron donor and acceptor moieties affects the photovoltaic processes. Also, the dyes having 2-(4-(4,4-dicyanobut-3-en-2-ylidene)cyclohexa-2,5-dien-1-ylidene)malononitrile electron acceptor (AQ and TQ) have better charge transfer indices such as longer charge transfer distance (DCT) and lower overlap of electron-hole distribution (S) in comparison with the dyes having 1,1,4,4-tetracyanobuta-1,3-dienes as an electron acceptor (AE and TE). Moreover, the properties of the absorption spectra indicate that TCNQ-adduct dyes (AQ and TQ) illustrate a red-shift compared with TCNE-adduct dyes (AE and TE) due to the higher ability of the electron-withdrawing. Finally, AQ and TQ dyes are the preferred candidates to improve the efficiency of the studied DSSCs because of higher charge transfer, electron transfer rate constant, and lower chemical hardness.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.