全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

DFT Study of the Reactivity of Some Methylenepyran Derivatives Used in Dye-Sensitized Solar Cells

DOI: 10.4236/cc.2026.144006, PP. 95-104

Keywords: Methylenepyran, Dyes, HOMO-LUMO Energy Gap, UV-Visible, DFT

Full-Text   Cite this paper   Add to My Lib

Abstract:

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. Angewandte Chemie International Edition, 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. The Journal of Organic Chemistry, 89, 13192-13207.
https://doi.org/10.1021/acs.joc.4c01328
[3]  Gr?tzel, M. (2003) Dye-Sensitized Solar Cells. Journal of Photochemistry and Photobiology C: Photochemistry Reviews, 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. International Journal of Electrochemical Science, 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. Solar Energy Materials and Solar Cells, 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. Solar Energy Materials and Solar Cells, 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. Solar Energy Materials and Solar Cells, 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. Journal of Physics: Conference Series, 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. Dyes and Pigments, 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. Organic Electronics, 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. Dyes and Pigments, 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. Chemistry Letters, 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. The Journal of Chemical Physics, 98, 5648-5652.
https://doi.org/10.1063/1.464913
[16]  Hay, P.J. and Wadt, W.R. (1985) ab Initio Effective Core Potentials for Molecular Calculations. Potentials for the Transition Metal Atoms Sc to Hg. The Journal of Chemical Physics, 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. The Journal of Chemical Physics, 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. Advances in Quantum Chemistry, 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. The Journal of Organic Chemistry, 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. The Journal of Chemical Physics, 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. The Journal of Chemical Physics, 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. Dyes and Pigments, 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. International Journal of Quantum Chemistry, 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. Results in Chemistry, 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. Chemical Physics Impact, 10, Article ID: 100789.
https://doi.org/10.1016/j.chphi.2024.100789

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133