Solar energy is one of the best alternatives for combating climate change. Its development has led to the creation of dye-sensitized solar cells (DSSCs). To improve the solar energy conversion efficiency of DSSCs, several organic compounds, including methylenepyran derivatives, have been synthesized. This work contributes to the understanding of some methylenepyran derivatives as dyes. To do this, the physicochemical and photovoltaic properties are evaluated through the dipole moment, the HOMO-LUMO energy gap, UV-Visible absorptions, and the Light Harvesting Efficiency (LHE). The calculations are carried out with DFT and TD-DFT methods in gas and aqueous phases. In both phases, the results show that compound CP, containing the phenyl group, is favorable for good intramolecular charge transfer, while compound CI, with the iodine substituent, is favorable for good light harvesting. CP and CI compounds are the best dyes among the six that were the subjects of this study.
References
[1]
Mishra, A., Fischer, M.K.R. and B?uerle, P. (2009) Metal-Free Organic Dyes for Dye‐Sensitized Solar Cells: From Structure: Property Relationships to Design Rules. AngewandteChemieInternationalEdition, 48, 2474-2499. https://doi.org/10.1002/anie.200804709
[2]
Erden, K., Soyler, D., Barsella, A., ?ahin, O., Soylemez, S. and Dengiz, C. (2024) Synthesis and Optical Characterization of Hydrazone-Substituted Push-Pull-Type NLOphores. TheJournalofOrganicChemistry, 89, 13192-13207. https://doi.org/10.1021/acs.joc.4c01328
[3]
Gr?tzel, M. (2003) Dye-Sensitized Solar Cells. JournalofPhotochemistryandPhotobiologyC: PhotochemistryReviews, 4, 145-153. https://doi.org/10.1016/s1389-5567(03)00026-1
[4]
Wei, D. and Amaratunga, G. (2007) Photoelectrochemical Cell and Its Applications in Optoelectronics. InternationalJournalofElectrochemicalScience, 2, 897-912. https://doi.org/10.1016/s1452-3981(23)17121-5
[5]
Calogero, G. and Marco, G.D. (2008) Red Sicilian Orange and Purple Eggplant Fruits as Natural Sensitizers for Dye-Sensitized Solar Cells. SolarEnergyMaterialsandSolarCells, 92, 1341-1346. https://doi.org/10.1016/j.solmat.2008.05.007
[6]
Wongcharee, K., Meeyoo, V. and Chavadej, S. (2007) Dye-Sensitized Solar Cell Using Natural Dyes Extracted from Rosella and Blue Pea Flowers. SolarEnergyMaterialsandSolarCells, 91, 566-571. https://doi.org/10.1016/j.solmat.2006.11.005
[7]
Roy, M.S., Balraju, P., Kumar, M. and Sharma, G.D. (2008) Dye-Sensitized Solar Cell Based on Rose Bengal Dye and Nanocrystalline TiO2. SolarEnergyMaterialsandSolarCells, 92, 909-913. https://doi.org/10.1016/j.solmat.2008.02.022
[8]
Wang, X., Bolag, A., Yun, W., Zhang, X., Bao, T., Ning, J., et al. (2020) Synthesis, Characterization and Dye-Sensitized Solar Cell Application of a Novel Symmetric Diphenylpyran Dye with Dual Rhodamine-3-Acetic Acid Anchors. JournalofPhysics: ConferenceSeries, 1549, Article ID: 032072. https://doi.org/10.1088/1742-6596/1549/3/032072
[9]
Verbitskiy, E.V., Cheprakova, E.M., Subbotina, J.O., Schepochkin, A.V., Slepukhin, P.A., Rusinov, G.L., et al. (2014) Synthesis, Spectral and Electrochemical Properties of Pyrimidine-Containing Dyes as Photosensitizers for Dye-Sensitized Solar Cells. DyesandPigments, 100, 201-214. https://doi.org/10.1016/j.dyepig.2013.09.006
[10]
Bolag, A., Nishida, J., Hara, K. and Yamashita, Y. (2012) Enhanced Performance of Dye-Sensitized Solar Cells with Novel 2,6-Diphenyl-4H-Pyranylidene Dyes. OrganicElectronics, 13, 425-431. https://doi.org/10.1016/j.orgel.2011.11.020
[11]
Solanke, P., Achelle, S., Cabon, N., Pytela, O., Barsella, A., Caro, B., et al. (2016) Proaromatic Pyranylidene Chalcogen Analogues and Cyclopenta[c]Thiophen-4,6-Dione as Electron Donors and Acceptor in Efficient Charge-Transfer Chromophores. DyesandPigments, 134, 129-138. https://doi.org/10.1016/j.dyepig.2016.07.008
[12]
Gauthier, S., Vologdin, N., Achelle, S., Barsella, A., Caro, B. and Robin-le Guen, F. (2013) Methylenepyran Based Dipolar and Quadrupolar Dyes: Synthesis, Electrochemical and Photochemical Properties. Tetrahedron, 69, 8392-8399. https://doi.org/10.1016/j.tet.2013.07.066
[13]
Bolag, A., Nishida, J., Hara, K. and Yamashita, Y. (2011) Dye-Sensitized Solar Cells Based on Novel Diphenylpyran Derivatives. ChemistryLetters, 40, 510-511. https://doi.org/10.1246/cl.2011.510
[14]
Parr, R.G. (1980) Density Functional Theory of Atoms and Molecules. In: Fukui, K. and Pullman, B., Eds., Horizons of Quantum Chemistry, Vol. 3, Springer. https://doi.org/10.1007/978-94-009-9027-2_2
[15]
Becke, A.D. (1993) Density-Functional Thermochemistry. III. The Role of Exact Exchange. TheJournalofChemicalPhysics, 98, 5648-5652. https://doi.org/10.1063/1.464913
[16]
Hay, P.J. and Wadt, W.R. (1985) abInitio Effective Core Potentials for Molecular Calculations. Potentials for the Transition Metal Atoms Sc to Hg. TheJournalofChemicalPhysics, 82, 270-283. https://doi.org/10.1063/1.448799
[17]
Burke, K., Werschnik, J. and Gross, E.K.U. (2005) Time-Dependent Density Functional Theory: Past, Present, and Future. TheJournalofChemicalPhysics, 123, Article ID: 062206. https://doi.org/10.1063/1.1904586
[18]
Amovilli, C., Barone, V., Cammi, R., Cancès, E., Cossi, M., Mennucci, B., et al. (1998) Recent Advances in the Description of Solvent Effects with the Polarizable Continuum Model. AdvancesinQuantumChemistry, 32, 227-261. https://doi.org/10.1016/s0065-3276(08)60416-5
[19]
Frisch, M.J., Trucks, G.W., Schlegel, H.B., Scuseria, G.E., Robb, M.A., Cheeseman, J.R., et al. (2009) Gaussian09, Revision A.02. Gaussian, Inc.
[20]
Raimundo, J., Blanchard, P., Gallego-Planas, N., Mercier, N., Ledoux-Rak, I., Hierle, R., et al. (2001) Design and Synthesis of Push-Pull Chromophores for Second-Order Nonlinear Optics Derived from Rigidified Thiophene-Based Π-Conjugating Spacers. TheJournalofOrganicChemistry, 67, 205-218. https://doi.org/10.1021/jo010713f
[21]
Oudar, J.L. and Chemla, D.S. (1977) Hyperpolarizabilities of the Nitroanilines and Their Relations to the Excited State Dipole Moment. TheJournalofChemicalPhysics, 66, 2664-2668. https://doi.org/10.1063/1.434213
[22]
Oudar, J.L. (1977) Optical Nonlinearities of Conjugated Molecules. Stilbene Derivatives and Highly Polar Aromatic Compounds. TheJournalofChemicalPhysics, 67, 446-457. https://doi.org/10.1063/1.434888
[23]
Koopmans, T. (1934) über die Zuordnung von Wellenfunktionen und Eigenwerten zu den Einzelnen Elektronen Eines Atoms. Physica, 1, 104-113. https://doi.org/10.1016/s0031-8914(34)90011-2
[24]
Zhang, J., Kan, Y., Li, H., Geng, Y., Wu, Y. and Su, Z. (2012) How to Design Proper Π-Spacer Order of the D-π-A Dyes for DSSCs? A Density Functional Response. DyesandPigments, 95, 313-321. https://doi.org/10.1016/j.dyepig.2012.05.020
[25]
Manzoor, T., Niaz, S. and Pandith, A.H. (2019) Exploring the Effect of Different Coumarin Donors on the Optical and Photovoltaic Properties of Azo-Bridged Push-Pull Systems: A Theoretical Approach. InternationalJournalofQuantumChemistry, 119, e25979. https://doi.org/10.1002/qua.25979
[26]
Manzoor, T. and Pandith, A.H. (2018) Theoretical Studies on the Structure, Optoelectronic and Photosensitizer Applications of NKX Class of Coumarin Dye Molecules. ChemistrySelect, 3, 2376-2385. https://doi.org/10.1002/slct.201702948
[27]
Ogunyemi, B.T., Oyeneyin, O.E., Esan, O.T. and Adejoro, I.A. (2020) Computational Modelling and Characterisation of Phosphole Adopted in Triphenyl Amine Photosensitisers for Solar Cell Applications. ResultsinChemistry, 2, Article ID: 100069. https://doi.org/10.1016/j.rechem.2020.100069
[28]
Verma, P. and Chetti, P. (2025) Investigation of the Influence of Donor and Internal Acceptor on Photovoltaic Parameters in D-A1-π-A Dye Sensitizers for Efficient DSSCs. ChemicalPhysicsImpact, 10, Article ID: 100789. https://doi.org/10.1016/j.chphi.2024.100789