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Photovoltaic properties of novel reactive azobenzoquinolines: experimental and theoretical investigations

  • Ededet A. Eno , Hitler Louis EMAIL logo , Tomsmith O. Unimuke , Ernest C. Agwamba , Anita T. Etim , Justina I. Mbonu , Henry O. Edet , ThankGod Egemoye , Kayode A. Adegoke and Umar S. Ameuru
Published/Copyright: December 12, 2023
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Abstract

In this work, synthesis, characterization, DFT, TD-DFT study of some novel reactive azobenzoquinoline dye structures to elucidate their photovoltaic properties. The azobenzoquinoline compounds were experimentally synthesized through a series of reaction routes starting from acenaphthene to obtained aminododecylnaphthalimide and finally coupled with diazonium salts to get the desired azobenzoquinoline. Azo dye synthesized differ in the number of alkyl chains designated as (AR1, AR2, AR3, and AR4) which were experimentally analyzed using FT-IR and NMR spectroscopic methods. The synthesized structures were modelled for computational investigation using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) combined with B3LYP and 6-31+G(d) basis set level of theory. The results showed that the HOMO-LUMO energy gap was steady at approximately 2.8 eV as the alkyl chain increases, which has been proven to be within the material energy gap limit for application in photovoltaic. The highest intramolecular natural bond orbital (NBO) for the studied compounds is 27.60, 55.06, 55.06, and 55.04 kcal/mol for AR1, AR2, AR3, and AR4 respectively and the donor and acceptor interacting orbitals for the highest stabilization energy (E (2)) are LP(1)N 18 and π*C 16O 19 respectively. The photovoltaic properties in terms of light-harvesting efficiency (LHE), Short circuit current density (J SC), Gibbs free energy of injection (ΔG inj), open-circuit voltage (V OC) and Gibbs free energy of regeneration (ΔG reg) were evaluated to be within the required limit for DSSC design. Overall, the obtained theoretical photovoltaic results were compared with other experimental and computational findings, thus, are in excellent agreement for organic solar cell design.


Corresponding author: Hitler Louis, Department of Pure and Applied Chemistry, University of Calabar, Calabar, Nigeria, E-mail:

Acknowledgment

The authors are thankful to all those who have supported this work in any way.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This research has not received funding from any repository.

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/psr-2021-0191).


Received: 2021-10-31
Accepted: 2022-03-28
Published Online: 2023-12-12

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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