Two polymer donors, FTAZ and J71 , and two fused-ring electron acceptors, ITIC1 and ITIC2 , are used to investigate the effects of conjugation dimension on the performance of organic solar cells (OSCs). FTAZ and J71 , and ITIC1 and ITIC2 share the same molecular backbone, respectively, while J71 and ITIC2 possess conjugated thienyl side chains. The addition of conjugated side chains slightly red-shifts the absorption spectra and lowers the bandgap due to the extended 2D conjugation. Conjugated side chains on the acceptor induce the self-aggregation of the acceptors, while conjugated side chains on the donor increase the miscibility of the donors and acceptors, thus optimizing the morphology of the active layers. The blends based on mixed combinations, namely 1D donor/2D acceptor and 2D donor/1D acceptor, show better performance relative to 1D donor/1D acceptor and 2D donor/2D acceptor.
more »
« less
Designing Thiadiazoloquinoxaline-Based Conjugated Polymers for Efficient Organic Photovoltaics: A DFT/TDDFT Study
Clean and renewable energy development is becoming frontier research for future energy resources, as renewable energy offers sustainable and environmentally friendly alternatives to non-renewable sources such as fossil fuels. Among various renewable energy sources, tremendous progress has been made in converting solar energy to electric energy by developing efficient organic photovoltaics. Organic photovoltaic materials comprising conjugated polymers (CP) with narrow optical energy gaps are promising candidates for developing sustainable sources due to their potentially lower manufacturing costs. Organic semiconductor materials with a high electron affinity are required for many optoelectronic applications. We have designed a series of organic semiconductors comprised of cyclopentadithiophene as a donor and thiadiazoloquinoxaline (TQ) as an acceptor, varying the π-conjugation and TQ-derivatives. We have employed density functional theory (DFT) and time-dependent DFT (TDDFT) to evaluate the designed CP’s optoelectronic properties, such as optical energy gap, dipole moment, and absorption spectra. Our DFT/TDDFT result shows that the energy gap of CPs is lowered and redshifted in the absorption spectra if there is no insertion of conjugation units such as thiophene and selenophene between donor and acceptor. In addition, selenophene shows relatively better redshift behavior compared to thiophene. Our work also provides rational insight into designing donor/acceptor-based CPs for organic solar cells.
more »
« less
- Award ID(s):
- 1757220
- PAR ID:
- 10578740
- Publisher / Repository:
- MDPI
- Date Published:
- Journal Name:
- Molecules
- Volume:
- 29
- Issue:
- 7
- ISSN:
- 1420-3049
- Page Range / eLocation ID:
- 1580
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
null (Ed.)Understanding the structural parameters that determine the extension of π-conjugation in 2-dimensions is key for controlling the optical, photophysical, and electronic properties of 2D-π-conjugated materials. In this article, three non-slanted H-mers including a donor–acceptor H-mer (H-mer-3) with an increase in dihedral angle (twist) between the strands and rungs are synthesized and studied. These non-slanted H-mers represent the repeat units of 2D-π-conjugated materials. H-mer-3, containing donor-strands and an acceptor-rung, is an unexplored donor–acceptor architecture in both slanted and non-slanted H-mers. The H-mers displayed both acid and base dependent optical properties. While the rungs have a little impact on the H-mer absorption spectra they play a key role in the emission and fluorescence lifetime. H-mer-3 ( i.e. , donor–acceptor H-mer) shows a higher Stokes shift and fluorescence lifetime than the other two H-mers. The twist and the presence of an electron deficient rung in H-mer-3 facilitated an intramolecular charge transfer in the excited state from the strands to the electron deficient rung, and therefore control over the H-mer emission properties. The lack of insulating pendant chains, reduced π–π interactions in thinfilms, and longer fluorescence lifetimes make these H-mers interesting candidates for various electronic and optoelectronic applications.more » « less
-
The design of organic light emitting diode (OLED) materials with the potential for exhibiting thermally-activated delayed fluorescence (TADF) is reported. Using computational methods (DFT/TD-DFT) as a guiding tool, six materials with a benzobisoxazole (BBO) core and donor–acceptor–donor architectures were designed by changing the conjugation position of carbazole-substituted phenyl substituents and the type of BBO isomer ( cis - vs. trans -). Experimental steady-state and transient absorption spectroscopic techniques were utilized to probe the TADF activity of these molecules. Each material was then used in host–guest OLED devices as either near-UV dopants or host with low singlet-triplet energy differences. The electroluminescent properties show that when used as dopants these materials provide near-UV emission (CIE y < 0.06 and CIE x = 0.16), whereas when used as hosts, these materials show reduced operating voltages and increased performance efficiencies when compared to commercial materials.more » « less
-
Ten novel fullerene-derivatives (FDs) of C60 and C70 had been designed as acceptor for polymer solar cell (PSC) by employing the quantitative structure-property relationship (QSPR) model, which was developed strategically with a reasonably big pool of experimental power conversion efficiency (PCE) data. The QSPR model was checked and validated with stringent parameter and reliability of predicted PCE values of all designed FDs. They were assessed by the applicability domain (AD) and process randomization test. The predicted PCE of FDs range from 7.96 to 23.01. The obtained encouraging results led us to the additional theoretical analysis of the energetics and UV-Vis spectra of isolated dyes employing Density functional theory (DFT) and Time-dependent-DFT (TD-DFT) calculations using PBE/6-31G(d,p) and CAM-B3LYP/6-311G(d,p) level calculations, respectively. The FD4 is the best C60-derivatives candidates for PSCs as it has the lowest exciton binding energy, up-shifted lowest unoccupied molecular orbital (LUMO) energy level to increase open-circuit voltage (VOC) and strong absorption in the UV region. In case of C70-derivatives, FD7 is potential candidate for future PSCs due to its strong absorption in UV-Vis region and lower exciton binding energy with higher VOC. Our optoelectronic results strongly support the developed QSPR model equation. Analyzing QSPR model and optoelectronic parameters, we concluded that the FD1, FD2, FD4, and FD10 are the most potential candidates for acceptor fragment of fullerene-based PSC. The outcomes of tactical molecular design followed by the investigation of optoelectronic features are suggested to be employed as a significant resource for the synthesis of FDs as an acceptor of PSCs.more » « less
-
We compared an indacenodithiophene(IDT)-based fused-ring electron acceptor IDIC1 with its counterpart IHIC1 in which the central benzene unit is replaced by a naphthalene unit, and investigated the effects of the benzene/naphthalene core on the optical and electronic properties as well as on the performance of organic solar cells (OSCs). Compared with benzene-cored IDIC1, naphthalene-cored IHIC1 shows a larger π-conjugation with stronger intermolecular π–π stacking. Relative to benzene-cored IDIC1, naphthalene-cored IHIC1 shows a higher lowest unoccupied molecular orbital energy level (IHIC1: −3.75 eV, IDIC1: −3.81 eV) and a higher electron mobility (IHIC1: 3.0 × 10 −4 cm 2 V −1 s −1 , IDIC1: 1.5 × 10 −4 cm 2 V −1 s −1 ). When paired with the polymer donor FTAZ that has matched energy levels and a complementary absorption spectrum, IHIC1-based OSCs show higher values of open-circuit voltage, short-circuit current density, fill factor and power conversion efficiency relative to those of the IDIC1-based control devices. These results demonstrate that extending benzene in IDT to naphthalene is a promising approach to upshift energy levels, enhance electron mobility, and finally achieve higher efficiency in nonfullerene acceptor-based OSCs.more » « less