TY - JOUR
T1 - Molecular design of new hydrazone dyes for dye-sensitized solar cells: Synthesis, characterization and DFT study
AU - Al-Sehemi, Abdullah G.
AU - Irfan, Ahmad
AU - Asiri, Abdullah M.
AU - Ammar, Yousry Ahmed
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): 08-NAN155-7
Acknowledgements: The present work has been carried out under Project No. 08-NAN155-7 funded by KAUST (King Abdul Aziz City for Science and Technology) through the Long Term Comprehensive National Plan for Science, Technology and Innovation program.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2012/7
Y1 - 2012/7
N2 - Three new sensitizers 2-{4-[2-(4-Nitrobenzylidene)hydrazino)]phenyl} ethylene-1,1,2-tricarbonitrile (NBHPET), 2-{4-[2-p-Chlorobenzylidenehydrazino] phenyl}- ethylene-1,1,2-tri carbonitrile (CBHPET) and 2-{4-[2-p- Bromobenzylidenehydrazino] phenyl}ethylene-1,1,2-tricarbonitrile (BBHPET) have been synthesized. The dyes showed pronounced solvatochromic effects as the polarity of the solvents increased. The structures have been optimized at B3LYP/6-31G(d) level of theory. The torsion in E-isomer is smaller than Z-isomer and azo isomers. The highest occupied molecular orbitals are delocalized on whole molecule while lowest unoccupied molecular orbitals are distributed on the tricarbonitrile. The lowest unoccupied molecular orbital energies are above the conduction band of titanium dioxide, highest occupied molecular orbitals of the dyes are below the redox couple of new synthesized dyes and small energy gap revealed these dyes would be better sensitizers for dye-sensitized solar cells. © 2012 Elsevier B.V. All rights reserved.
AB - Three new sensitizers 2-{4-[2-(4-Nitrobenzylidene)hydrazino)]phenyl} ethylene-1,1,2-tricarbonitrile (NBHPET), 2-{4-[2-p-Chlorobenzylidenehydrazino] phenyl}- ethylene-1,1,2-tri carbonitrile (CBHPET) and 2-{4-[2-p- Bromobenzylidenehydrazino] phenyl}ethylene-1,1,2-tricarbonitrile (BBHPET) have been synthesized. The dyes showed pronounced solvatochromic effects as the polarity of the solvents increased. The structures have been optimized at B3LYP/6-31G(d) level of theory. The torsion in E-isomer is smaller than Z-isomer and azo isomers. The highest occupied molecular orbitals are delocalized on whole molecule while lowest unoccupied molecular orbitals are distributed on the tricarbonitrile. The lowest unoccupied molecular orbital energies are above the conduction band of titanium dioxide, highest occupied molecular orbitals of the dyes are below the redox couple of new synthesized dyes and small energy gap revealed these dyes would be better sensitizers for dye-sensitized solar cells. © 2012 Elsevier B.V. All rights reserved.
UR - http://hdl.handle.net/10754/598873
UR - https://linkinghub.elsevier.com/retrieve/pii/S0022286012001494
UR - http://www.scopus.com/inward/record.url?scp=84861801705&partnerID=8YFLogxK
U2 - 10.1016/j.molstruc.2012.02.035
DO - 10.1016/j.molstruc.2012.02.035
M3 - Article
SN - 0022-2860
VL - 1019
SP - 130
EP - 134
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
ER -