- Research article
- Open Access
DFT and TD-DFT calculation of new thienopyrazine-based small molecules for organic solar cells
© The Author(s) 2016
Received: 28 February 2016
Accepted: 20 October 2016
Published: 27 October 2016
Novel six organic donor-π-acceptor molecules (D-π-A) used for Bulk Heterojunction organic solar cells (BHJ), based on thienopyrazine were studied by density functional theory (DFT) and time-dependent DFT (TD-DFT) approaches, to shed light on how the π-conjugation order influence the performance of the solar cells. The electron acceptor group was 2-cyanoacrylic for all compounds, whereas the electron donor unit was varied and the influence was investigated.
The TD-DFT method, combined with a hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP) in conjunction with a polarizable continuum model of salvation (PCM) together with a 6-31G(d,p) basis set, was used to predict the excitation energies, the absorption and the emission spectra of all molecules.
The trend of the calculated HOMO–LUMO gaps nicely compares with the spectral data. In addition, the estimated values of the open-circuit photovoltage (Voc) for these compounds were presented in two cases/PC60BM and/PC71BM.
The study of structural, electronics and optical properties for these compounds could help to design more efficient functional photovoltaic organic materials.
The organic bulk heterojunction solar cells (BHJ) are considered as one of the promising alternative used for renewable energy. This is attributed to their several advantages to fabricate the flexible large-area devices and also to their low cost compared to other alternatives based on inorganic materials [1, 2]. Generally, the organic BHJ solar cells based on the mixture of electron donor (material organic) and electron acceptor materials as PCBM or its derivatives and have been utilized in the aim to harvest the sunlight. Over the past few years, considerable effort has been focused on improving organic solar cells (OSC) performance to achieve power conversion efficiencies (PCE) of 10%. The following strategies have been adopted for this purpose [3–13]: (1) design of the new photoactive materials able to increase the efficiency of photoconversion such as fullerenes and π-conjugated semiconducting polymers; (2) use of functional layers of buffering, charge transport, optical spacing, etc., and; (3) morphological tuning of photoactive films by post-annealing, solvent drying, or processing by using additives. After many efforts, the design of the organic BHJ solar cells based on polymer semiconducting (PSCs) as an electron donating and PCBM as an electron accepting showed impressive performances in converting solar energy to electrical energy. Finally, the power conversion efficiency (PCE) was improved in the range of 7–9.2% [14–21] for single layer PSCs and 10.6%  for tandem structured PSCs. These kinds of solar cells based on polymers have potential applications in next-generation solar cells compared to dye-sensitized solar cells (DSSC) and inorganic thin-film. On the other hand, considerable research has been directed to developing an efficient small-molecule organic used as a semiconductors and to improve their performance in the organic solar cells (OSCs), with the near-term goal of achieving a PCE comparable to that of polymer solar cells (PSCs) [22–24].
Small-molecule organic semi-conductors are more suitable than polymer-based ones for mass production because the latter suffer from poor reproducibility of the average molecular weight, high dispersity, and difficulties in purification. Recently, the small molecule for organic solar cells (SMOSCs) with PCEs exceeding 6% have been reported  thus making solution-processed SMOSCs strong competitors to PSCs. This inspires us to develop a new low band gap for small molecules for organic solar cells application. In order to achieve high current density in SMOSCs, utilizing new donor molecules that can efficiently absorb the sunlight at the maximum solar flux region (500–900 nm) of the solar spectrum, because the energy conversion efficiency of the small molecule for organic solar cells is directly attached to the light harvesting ability of the electron donor molecules. In addition, to get high open circuit voltage (Voc), the HOMO levels of the donor molecules should be down a −5.0 eV, in which this factor is calculated by the difference between the HOMO and LUMO levels of the donor and acceptor materials, respectively. The most small molecule organic semiconductors used in solar cells have a push–pull structure comprising electron donors and acceptors in objective to enhance the intramolecular charge transfer (ICT) and the band gap becomes narrow and then, yielding higher molar absorptivity [22–25]. A common strategy to enhance the power conversion efficiency of low band gap conjugated molecules as an alternating (D-A) or (D-π-A) structures because this improves the excitation charge transfer and transport . Different authors described in recent studies the importance of compounds with D-π-A structure and their role in the elaboration of the organic solar cell [27–29]. The organic material based on thienopyrazine has been used as a donor unit; still receive considerable attention for their exceptional optoelectronic properties [30, 31]. Knowledge about the optoelectronic properties of these new materials can help with the design of new materials with optimized properties for solar energy conversion. In our previous works [32, 33], we have reported a theoretical study of photovoltaic properties on a series of D-π-A structures of thienopyrazine derivatives as photoactive components of organic BHJ solar cells.
In order to obtain materials with more predominant capability, the development of novel structures is now being undertaken following the molecular engineering guidelines, the theoretical studies on the electronic structures of these materials have been done in order to rationalization the properties of known ones and the prediction those of unknown ones . As is known, the knowledge of the HOMO and LUMO levels of the materials is crucial in studying organic solar cells. The HOMO and LUMO energy levels of the donor and of the acceptor compounds present an important factor for photovoltaic devices which determine if the charge transfer will be happen between donor and acceptor. The thienopyrazine derivatives would be much more promising for developing the panchromatic materials for photovoltaic, and thus, provide much higher efficiencies if new absorption bands could be created in the visible light region.
All calculations were carried out using density functional theory (DFT) with B3LYP (Becke three-parameter Lee–Yang–Parr) exchange-correlation functional . 6-31G(d,p) was used as a basis set for all atoms (C, N, H, O, S). Recently, Tretiak and Magyar  have demonstrated that the charge transfer states can be achieved in D-π-A structure a large fraction of HF exchange is used. A newly designed, functional, the long range Coulomb-attenuating method (CAM-B3LYP) considered long-range interactions by comprising 81% of B88 and 19% of HF exchange at short-range and 35% of B88 and 65% of HF exchange at long-range . Furthermore, The CAM-B3LYP has been used especially in recent work and was demonstrated its ability to predict the excitation energies and the absorption spectra of the D-π-A molecules [37–40]. Therefore, in this work, TD-CAM-B3LYP method has been used to simulate the vertical excitation energy and electronic absorption spectra. It is important to take into account the solvent effect on theoretical calculations when seeking to reproduce or predict the experimental spectra with a reasonable accuracy. Polarizable continuum model (PCM)  has emerged in the last two decades as the most effective tools to treat bulk solvent effects for both the ground and excited states. In this work, the integral equation formalism polarizable continuum model (IEF-PCM) [42, 43] was used to calculate the excitation energy. The oscillator strengths and excited state energies were investigated using TD-DFT calculations on the fully DFT optimized geometries.
all calculations were performed using the Gaussian 09 package .
Results and discussion
Ground state geometry
Optimized selected bond lengths and bond angles of the studied molecules obtained by B3LYP/6-31G(d,p) level [the unit of bond lengths is angstroms (Å), the bond angles and dihedral angles is degree (°)]
As shown in Table 1, all calculations have been done by using DFT/B3LYP/6-31G(d,p) level. The large torsional angle Φ1 of the compounds P1, P2, P3, P4, P5 and P6 suggest that strong steric hindrance exists between the donor and π-spacer.
For P2, the dihedral angles Φ1 formed between the donor group and π-spacer is 0.78°, indicating a smaller conjugation effect compared to the other compounds where the coplanarity can be observed, but this geometry of P2 allows inhibiting the formation of π-stacked aggregation efficiently. Furthermore, the dihedral angles Φ2 of all compounds is very small (2.77, 2.95, 2.85, 2.82, 2.84 and 2.76) wich indicates that the acceptor (cyanoacrylic unit) is coplanar with π-spacer (thiophene–thienopyrazine–thiophene). In the excited state (S1), we remark that the dihedral angles Φ1 for all compounds are significantly decreased in comparison with those in the ground state (S0), except P2 and P6, Φ1 is almost similar to that of the ground state. It indicates that the nature of the S1 state of the molecular skeleton of all compounds is different from the S0 state, and the complete coplanarity in S1 state triggers the fast transfer of the photo-induced electron from S0 to S1.
The shorter value from the length of bridge bonds between π-spacer and the donor (LB1) and in another side between π-spacer and acceptor (LB2) favored the ICT within the D-π-A molecules. However, in the ground state (S0) the calculated critical bond lengths LB1 and LB2 are in the range of 1.421–1.462 Å showing especially more C=C character, except the compound P6, which enhances the π-electron delocalization and thus decreases the LB of the studied compounds and then favors intramolecular charge transfer ICT. On the other hand, upon photoexcitation to the excited state (S1), the bond lengths and torsional angles for these compounds significantly decreased in comparison with those in the ground state (S0), especially the linkage between the π-spacer and the acceptor moiety (LB2). These results indicate that the connection of acceptor group (2-cyanoacrylic acid) and the π-bridge is crucial for highly enhanced ICT character, which is important for the absorption spectra red-shift.
Among electronic applications of these materials is their use as organic solar cells, we note that theoretical knowledge of the HOMO and LUMO energy levels of the components is crucial in studying organic solar cells. The HOMO and LUMO energy levels of the donor and of the acceptor components for photovoltaic devices are very important factors to determine whether the effective charge transfer will happen between donor and acceptor. The experiment showed that the HOMO and LUMO energies were obtained from an empirical formula based on the onset of the oxidation and reduction peaks measured by cyclic voltammetry. But in the theory, the HOMO and LUMO energies can be calculated by DFT calculation. However, it is noticeable that solid-state packing effects are not included in the DFT calculations, which tend to affect the HOMO and LUMO energy levels in a thin film compared to an isolated molecule as considered in the calculations. Even if these calculated energy levels are not accurate, it is possible to use them to get information by comparing similar oligomers or polymers.
Calculated EHOMO, ELUMO levels, energy gap (Eg), dipole moment (ρ) and other quantum parameters chemical as electronegativity (χ), chemical potential (μ) and chemical hardness (η) values of the studied compounds obtained by B3LYP/6-31G(d,p) level
Quantum chemical parameters
Generally, the molecules having a large dipole moment, possesses a strong asymmetry in the distribution of electronic charge, therefore can be more reactive and be sensitive to change its electronic structure and its electronic properties under an external electric field. Through the Table 2, we can observe that the dipole moment (ρ) of compounds P1 and P4 are greater than others compounds, therefore we can say that these compound are more reactive that other compound, indeed, these compounds are more favorite to liberate the electrons to PCBM.
On another side, we note that the PCBM has the smallest value of the chemical potential (μ = −4.9) compared to six compounds (P1, P2, P3, P4, P5, and P6) (see Table 2), this is a tendency to view the electrons to escape from compound Pi has a high chemical potential to PCBM which has a small chemical potential, therefore PCBM behaves as an acceptor of electrons and others compounds Pi behave as a donor of electrons. For the electronegativity, we remark that the PCBM has a high value of electronegativity than other compounds (P1, P2, P3, P4, P5, and P6) (Table 2), thus the PCBM is the compound that is able to attract to him the electrons from others compounds. In another hand, we remark that the PCBM compound has a high value of chemical hardness (η) in comparison with other six compounds, this indicates that the PCBM is very difficult to liberate the electrons, while the other compounds are good candidates to give electrons to the PCBM (see Table 2).
where the JSC is estimated by the maximum current which flows in the device under illumination when no voltage is applied, in which dependent on the morphology of the device and on the lifetime and the mobility of the charge carriers .
The maximum open-circuit voltage (Voc) of the BHJ is determined by the difference between the HOMO of the donor (π-conjugated molecule) and the LUMO of the acceptor, taking into account the energy lost during the photo-charge generation [47, 48]. It has been found that the VOC is not very dependent on the work functions of the electrodes [49, 50].
In addition, low LUMO of the π-conjugated compounds and a high LUMO of the acceptor of the electron (PC71BM, PC60BM) increase the value of VOC, which contributes a high efficiency of the solar cells [48, 50].
Energy values of ELUMO (eV), EHOMO (eV), Egap (eV) and the open circuit Voltage Voc (eV) and LUMOdonor−LUMOacceptorof the studied molecules obtained by B3LYP/6-31G(d,p) level
LD − LA(PC60BM)
LD − LA(PC71BM)
Therefore, all the studied molecules can be used as BHJ because the electron injection process from the excited molecule to the conduction band of PCBM and the subsequent regeneration is possible in an organic sensitized solar cell.
Absorption spectra data obtained by TD-DFT methods for the title compounds at CAM-B3LYP/6-31G(d,p) optimized geometries in the gas phase and in solvent phase (chloroform)
In the gas phase
In solvent phase
HOMO → LUMO
HOMO → LUMO
HOMO → LUMO
HOMO → LUMO
HOMO → LUMO
HOMO → LUMO
Emission spectra data obtained by TD-DFT methods for the title compounds at B3LYP/6–31G(d,p) optimized geometries in chloroform solvent
ʎmax emis (nm)
Radiative life times (ns)
LUMO → HOMO
LUMO → HOMO
LUMO → HOMO
LUMO → HOMO
LUMO → HOMO
LUMO → HOMO
Excited state lifetimes
where (c) is the velocity of light, E Flu is the excitation energy, and ƒ is the oscillator strength (O.S.). The computed lifetimes (τ), for the title compounds are listed in Table 5. However, an increase in lifetimes of Pi will retard the charge recombination process and enhance the efficiency of the photovoltaics cells. So, long radiative lifetimes facilitate the electron transfer upon the photoexcited electron, from LUMO of electron-donor to LUMO of electron-acceptor, thus lead to high light-emitting efficiency. The radiative lifetimes of the study compounds are from 7.61 to 7.11 ns and increases in the following order P4 < P1 < P2 < P5 < P3 < P6. This result is sufficient to obtain a high light-emitting efficiency, especially for P6.
We have used the density functional theory method to investigate the geometries and electronic properties of some thienopyrazine-derivatives in alternate donor-π-acceptor structure. The modification of chemical structures can greatly modulate and improve the electronic and optical properties of pristine studied materials. The electronic properties of new conjugated materials based on thienopyrazine and heterocyclic compounds and different acceptor moieties have been computed by using 6-31G(d,p) basis set at a density functional B3LYP level, in order to guide the synthesis of novel materials with specific electronic properties. The concluding remarks are:
The predicted band gaps by using DFT-B3LYP/6-31G(d,p) are in the range of 1.968–2.171 eV, knowing that the small band gap due to the increasing of the displacement of the electron between donor and acceptor spacer is very easy. The much lower Eg of P1, P2, and P3 compared to other compounds a significant effect of intramolecular charge transfer. However, the Eg values of P1, P2 and P3 are smaller than that of P6.
The theoretical values of the open circuit voltage Voc of the studied molecules range from 1.499 to 1.804 eV in the case of PC60BM and 0.425 to 0.73 eV in the case of PC71BM, these values are sufficient for a possible efficient electron injection. After the results, we note that all the studied molecules can be used as BHJ because the electron injection process from the excited molecule to the conduction band of PCBM and the subsequent regeneration is possible in an organic sensitized solar cell. It is concluded that We note that the higher power conversion efficiency could be achieved for P2 is 4 and 3% for P3.
The TD-DFT calculations, at least TD-CAM-B3LYP/6-31G(d,p) was used to replicate the optical transitions in order to predict the excited and emission states; the predicted result of the absorption wavelengths for P1, P2, P3, P4, P5, and P6 is 805.02, 794.65, 801.53, 793.82, 790.72 and 727.01 nm respectively.
The decreasing of the band gap of these six materials due to increasing the absorption wavelengths, then the best commands which can be used in photovoltaic cells such as donor of electronic, is one which has the small band gap and large wavelengths, thus all compounds (1–6) are appropriate to do this role.
MB, ATB, MB and MM done the quantum calculation, analyzed and interpreted the data of materials, analysis tools or data; wrote the paper. MH, SMB and MB proposed the studied compounds and checked the analyzed and interpreted the data of materials, analysis tools or data. All authors read and approved the final manuscript.
This work was supported by Volubilis Program (No MA/11/248), and the convention CNRST/CNRS (Project chimie 1009).
The authors declare that they have no competing interests.
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