Research Article  Open Access
Yuanzuo Li, Huixing Li, Peng Song, Chaofan Sun, "Photoactive Layer of DSSCS Based on Natural Dyes: A Study of Experiment and Theory", Journal of Nanomaterials, vol. 2015, Article ID 139382, 6 pages, 2015. https://doi.org/10.1155/2015/139382
Photoactive Layer of DSSCS Based on Natural Dyes: A Study of Experiment and Theory
Abstract
Three natural dyes (Forsythia suspensa, Herba Violae, and Corn leaf) have been investigated as potential sensitizers for dyesensitized solar cells. UVvis absorption spectra reveal that three natural dyes mainly contain the compound of pheophytin a. Among three DSSCs, the highest photo electronic conversion efficiency is 0.96% with open circuit voltage () of 0.66 V, short circuit current density () of 1.97 mA cm^{−2}, and fill factor (ff) of 0.74. Theoretical timedependent density functional theory and charge difference density are used to explore the nature of excited states. Results demonstrate that the first state is an intramolecular charge transfer (ICT) state, and electron injection could occur owing to the thermodynamically driving force.
1. Introduction
Since the initial report on dyesensitized solar cells (DSSCs) by Hagfeldt and Graetzel [1], much effort has been devoted toward designing and synthesizing metalfree photosensitizers to improve sunlight harvesting efficiency and yield efficient charge separation [2–5]. Most of the efficient DSSCs are sensitized with the dyes having ruthenium based complexes that have been shown to operate with power conversion around 10% using nanoporous TiO_{2} electrodes [6]. However, due to the high cost of ruthenium complexes and the long term unavailability of these noble metals [7], there is a need to search for alternative photosensitizers for the use in TiO_{2}based photovoltaic devices.
Recently, several studies have focused on the natural dyes as DSSCs sensitizers [8–15] because the natural dyes could be extracted from flowers, vegetables, wood, seed, fruits, and so forth, by using minimal chemical procedures. Several natural pigments such as anthocyanin [10–12], chlorophyll [13], tannin [14], and carotene [15] have been used as sensitizer in DSSCS, and the highest photoelectronic conversion efficiency based on natural dyes is around 2% [10, 11]. In this study, we extract three dyes from natural plants of Forsythia syspensa, Herba Violae, and Corn leaf to use as DSSCS and achieve the highest efficiency = 0.96% with a good fill factor of 0.74 under AM 1.5 using a density of power 100 mW/cm^{2}.
2. Methods
Forsythia suspensa (Fs), Herba Violae (Hv), and Corn leaf (Cl) were collected fresh and kept in a vacuum furnace by controlling temperature at 70°C to remove the moisture. The dried samples were crushed in a mortar to make them into powder, and then powdered samples were mixed into ethanol, and the concentration of three samples is 1 g/mL. After extraction for about a week under the opaque condition, further purification of the extracts was avoided in order to achieve efficient sensitization using simple extraction procedures. The structure of DSSCs is mainly composed of electrode, dyes, and electrolyte solution. The elaborated preparation procedure is listed as follows: (a) the TiO_{2} electrode was prepared; add 10 mL isopropyl titanate to water, and keep hydrolysis for 3 h; then add HNO_{3} and HAC to the solution, under 80°C; the mixed solution was stirred until it became transparent clear blue; later, at 200°C hydrothermal reaction was carried on for 12 h. After cooling and spin steaming, centrifugal, terpineol ethyl, and cellulose were added to the ball grinder; the paste was prepared completely by ball mill, rotary steam, and threeroll mill. (b) The application of screen printing technology was used, which printed the TiO_{2} paste to the clean surface of conductive glass, and the active area of cell was 0.16 cm^{2}; after ethanol bath and drying, the anode electrodes were sintered, and then the anode electrodes were treated in TiCl_{4} solution. In the next process, the anode electrodes were sintered as well, and after the processing, the anode immediately was removed after the natural cooling to 80°C, and the anode electrodes were soaked in the natural dye without light for 24 h. (c) The anode electrode and the platinum plating counter electrode were assembled into the cell, in the middle of the two electrodes, and the electrolyte solution was added (0.5 mol/L LiI, 0.05 mol/L I2 TBP, and GUSCN were included). UVvis spectra were measured with TU1900 spectrometer (Beijing, China), and the FTIR spectra were measured with FTIR 360 spectrometer (Nicolet, Madison, WI, USA). Solar energy conversion efficiency measurements were done with a solar simulation instrument (Pecell15, Japan), and light intensity was adjusted via a reference standard Sisolar solar cell at 1 sun light intensity of 100 mW cm^{−2}. Theoretically, the ground state optimization and absorption simulation were done with DFT/B3LYP [16–19] and TDDFT/CAMB3LYP [20, 21] using same basis set 631G(d). For comparison, M062x function was also used. All quantum chemical calculations were done with Gaussian 09 [22]. Quantum chemical calculations [23–27] and threedimensional (3D) realspace analyses [25, 26] were used to study the relationship between structures and the optical properties, which has been used to explain charge transfer and excited states properties of organic system.
3. Results and Discussion
UVvis absorption spectra of Forsythia suspensa (Fs), Herba Violae (Hv), and Corn leaf (Cl) in ethanol were shown in Figure 1(a), and for comparison, simulated absorption spectrum was shown in Figure 1(b), and the calculated data were listed in Table 1. It is found that the absorption spectra of three dyes cover the two absorption bands from 400 nm to 700 nm, and they display a strongest absorption band (666–669 nm) that corresponds to the red absorption band (666 nm) of pheophytin a [28, 29]. The calculation reproduces the two absorption spectra of dyes (see Figure 1(b)), and the first absorption in ethanol is found to be 595.51 nm () by using TDCAMB3LYP/631G(d)//B3LYP/631G(d), which makes a red shift of 50 nm compared with the first absorption peak with TDM062x/631G(d)//B3LYP/631G(d) ( = 545 nm).
 
Data from TDM062x/631G(d)//B3LYP/631G(d). 
(a)
(b)
The transition energy and oscillator strength were listed in Table 1. As shown in Table 1, it is found that the excited state is composed of electron transition from HOMO to LUMO with the weight of 0.62279. It is very important for DSSCS to perform well with energy match; that is, the HOMO energy level should be laid below the redox couple, and LUMO energy level should be higher than that of TiO_{2} semiconductor. Therefore, the energy level match is necessary for the optical electronic transfer and electron recovery in the system of solar cells. Comparison results show that the HOMO energy level is found to be −5.21 eV, which is lower than that of HOMO of the redox couple I^{−}/I^{3−} (−4.8 eV [28, 29]), which means that excited dye can obtain electron from the redox couple to recovery; and LUMO energy level is −2.736 eV, which is above the conduction band of TiO_{2}. The energy gap is 2.474 eV, and exciton binding energy can be obtained from the difference values between excitation energy and energy gap, which are 0.392 eV and 0.199 eV through the two functional evaluations of CamB3LYP and M062x, respectively.
Fourier transform infrared spectrum of three dyes in the range of 400–4000 cm^{−1} was measured experimentally, as shown in Figure 2(a). For comparison, a simulated spectrum in ethanol was also calculated theoretically (see Figure 2(b)). Figure 2(a) shows that the three dyes have similar shape and peak site of IR, and strong spectra of IR are found to be 3000–4000 cm^{−1} and 1000–2000 cm^{−1}, that is, 1107.15, 1398.74, 1634.78, 2359.23, 2924.52, and 3420.00 cm^{−1}, respectively. Figure 2(b) shows that there is a peak site of 3520 cm^{−1}, and it is a vibration of NH, as supported by the vibration analysis in Figure 3. From 3000 to 3200 cm^{−1} region, the vibration of 3072 cm^{−1} comes from the stretching vibration of CH on polyene hydrocarbon (see Figure 3). The stretching vibrations of C=O on the thiophene units and carboxyl group are 1752 cm^{−1} and 1795 cm^{−1}, respectively. The sharp and strong absorption peaks for C=C stretching mode and the out of plane of CH bending mode were 1660 cm^{−1} and 952 cm^{−1}, respectively.
(a)
(b)
Currentvoltage curves for Fs (black line), Hv (red line), and Cl (blue line) were shown in Figure 4, respectively. Table 2 shows  (currentvoltage) characteristics of the DSSCs sensitized with three dyes, which are composed of short circuit current density (), open circuit voltage (), fill factor (ff), and energy conversion efficiency (). The DSSCs sensitized with Herba Violae dye showed conversion efficiency () of 0.96%, with open circuit voltage () of 0.66 V, short circuit current density () of 1.97 mA cm^{−2}, and fill factor (ff) of 0.74. The DSSCs sensitized with Fs showed conversion efficiency () of 0.90%, and the open circuit voltage of Fs is smaller than that of Hv, but short circuit current density of Fs is larger than that of Hv. For three solar cells, the values of and for Cl are both smaller than the two other cells, and its conversion efficiency () is 0.47.

To better study the excited states properties of the dye, the 3D realspace analysis is employed, which successfully explained the excited states properties of oligomers and polymers [25–27]. The 3D realspace analysis was shown in Figure 5, and density of molecular orbital for HOMO and LUMO was shown in supporting materials Figure S1 in Supplementary Material available online at http://dx.doi.org/10.1155/2015/139382. From Figure S1, it is found that electron density distributions of the HOMO and LUMO are mainly located on the pheophytin body and there is no electron density under the polyene hydrocarbon, which are supported by charge difference density (CDD) analysis (see Figure 5). As shown, CDD shows that the excited state only occurs on the pheophytin body (where red and green represent the electron and hole, resp.). The state is an intramolecular charge transfer state (ICT) because the holes are located on the central rings, and electron is transferred into outside area. It is worth nothing that the red electrons are located on the attaching group C=O of pheophytin, and the increasing electron density upon the surface of semiconductor should be an important condition for the electron injection. The density of second state is similar to the first excited state. S3 and S4 are located excited states, and there is no electron upon attaching group. At the same time, the S6 excited state is also a located excited state (which is different with S3 and S4), and Figure 5 shows that excited electron and hole pair almost only appear upon the attaching group.
For DSSCs, excited electron should be quickly injected from the discontinuous energy level of dyes into the CB of the semiconductor titanium dioxide. Thermodynamically, driving force of the electron injection process can be described as the difference between excited state oxidation potential and CB edges. From Rehm and Weller equation [30], can be calculated as follows:where and are the excited and ground state oxidation potentials and is the electronic transition energy, and the ground state oxidation potential is computed from the HOMO energy. The value of is calculated to be −0.82 V which is more negative than the CB edge of TiO_{2} (0.5 V versus normal hydrogen electrode (NHE)) [31–33], and electron injection is more easy to occur owing to the bigger difference between the excited state oxidation potentials and CB edge.
4. Conclusions
Three DSSCs based on natural dyes extracted from Forsythia suspensa, Herba Violae, and Corn leaf have been studied, and optical electronic results show that the highest photoelectronic conversion efficiency = 0.96% with open circuit voltage () of 0.66 V, short circuit current density () of 1.97 mA cm^{−2}, and fill factor (ff) of 0.74. TDDFT calculations show that the objected system has wide absorption region, and charge difference density demonstrated that there is an ICT state for the S1 state and provided the orientation of charge transfer. Electron injection is thermodynamically permitted.
Conflict of Interests
The authors declare no conflict of interests.
Acknowledgments
This work was supported by the Fundamental Research Funds for the Central Universities (Grant no. 2572014CB31), the Heilongjiang Provincial Youth Science Foundation (Grant no. QC2013C006), and the National Natural Science Foundation of China (Grant nos. 11404055 and 11374353).
Supplementary Materials
Figure S1. Energy and electron density of HOMO and LUMO.
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Copyright © 2015 Yuanzuo Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.