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Thienochrysenocarbazole‐Based Dyes for Solar Cell: A Theoretical Investigation of the Tethering‐Position‐Related Influence of Triple‐Bond on the Electronic and Optical Properties
Author(s) -
Mu Yanfei,
Dong Guangxing,
Dong Xiandui,
Zhang Min
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201802746
Subject(s) - chemistry , triple bond , acceptor , density functional theory , organic solar cell , thiophene , moiety , band gap , dihedral angle , homo/lumo , photochemistry , computational chemistry , materials science , stereochemistry , molecule , double bond , hydrogen bond , organic chemistry , optoelectronics , polymer , physics , condensed matter physics
The development of organic dyes based on polycyclic aromatic hydrocarbons (PAHs) donors characteristic of coplanar skeleton in conjunction with acceptors involving benzothiadiazole unit recently brought forth consecutive improvement for dye‐sensitized solar cells (DSCs). In this paper, we systematically investigate the tethering‐position‐related influence of triple‐bond insertion on the intrinsic geometric, electronic and optical properties of organic dyes with PAHs as the central blocks based on the density functional theory. We consider two isomer donors, where a thienochrysenocarbazole (TCC) unit is substituted by alkoxyphenyl at either thiophene ( t ‐PTCC) or naphthalene ( n ‐PTCC) moiety, with benzothiadiazole‐benzoic acid acceptor linked to the donor either directly or through ethynyl linkage. The tethering‐position‐related torsion angle between the donor and acceptor plays a significant role in determining the electronic and optical properties of these sensitizers. The introduction of triple‐bond can bring forth improved coplanarity of skeleton as well as energy‐gap shrinkage; however, it also results in an increased distance between the spatial distributions of the frontier molecular orbitals. Our study has underlined that the resultant red or blue shifting of absorption spectrum induced by the triple‐bond insertion is jointly determined by the interplay between the overlap degree of frontier molecular orbitals and energy‐gap.