Literature DB >> 33855239

Influence of concentration of anthocyanins on electron transport in dye sensitized solar cells.

Alex Okello1, Brian Owino Owuor2, Jane Namukobe3, Denis Okello1, Julius Mwabora2.   

Abstract

The influence of concentration of anthocyanins in dye sensitized solar cells (DSSC) has been investigated, with focus on how concentration influence electron transport. The influence on electron transport was then linked to solar cell performance. Anthocyanins were extracted from fresh flowers of Acanthus pubscenes using methanol acidified with 0.5% trifluoracetic acid, concentrated using a rotary evaporator and partitioned against ethyl acetate. Concentration of the anthocyanins was determined using Keracyanin Chloride as a standard. DSSC were fabricated using Titanium dioxide as anode, anthocyanins as sensitizers and Platinum as counter electrode material. Titanium dioxide was deposited on Fluorine doped Tin oxide glass substrate using slot coating method. Platinum was deposited on FTO glass substrate using a brush previously dipped in plastisol precursor, and annealed at 450 0C for 20 min to activate Platinum. Dye sensitized solar cells were assembled using anthocyanins at varying concentrations. Performance parameters of the solar cells were measured using a solar simulator which was fitted with digital source meter. Electron transport parameters were studied using electrochemical impedance spectroscopy (EIS). Open circuit voltage, short circuit current and fill factor were observed to increase with concentration of anthocyanins. The increase in solar cell performance was attributed to increase in charge density which led more charges being available for transported to solar cell contacts. The increased charge resulted in a negative shift in Fermi level of electrons in the conduction band of TiO2. The shift in Fermi level resulted into an increase in open circuit voltage and the overall solar cell performance. EIS studies revealed increase in recombination resistance with concentration of anthocyanins. The increase in recombination resistance was found to be related to increase in electron density, and hence the shift in the Fermi level of electrons in the conduction band of TiO2.
© 2021 The Authors.

Entities:  

Keywords:  Dye sensitized solar cells; Electron lifetime; Fermi level; Impedance electron spectroscopy; Recombination resistance; Slot coating; TiO2

Year:  2021        PMID: 33855239      PMCID: PMC8027771          DOI: 10.1016/j.heliyon.2021.e06571

Source DB:  PubMed          Journal:  Heliyon        ISSN: 2405-8440


Introduction

The world today is facing a daunting task of mitigating the impact of greenhouse gasses emitted mostly from fossil sources of energy [1]. The greenhouse gasses emitted by the sources have led to global warming, and this has adverse effects on eco systems [2]. Because of the greenhouse gasses, there are now climate changes, and this coupled with growing energy demand and depletion of fossil resources, presents need for sustainable and environmentally friendly energy technology [3]. Fortunately, energy from the sun to the earths is about J per year [3]. This amount of energy, when harvested with a suitable technology and converted into electricity can meet all man's energy needs, while at the same time keeping the environment clean [1, 3, 4]. In the last few decades, researchers have therefore embarked on research to design technologies that can be used to harvest this energy [5]. A type of solar cell that has drawn attention since 1991 is the dye sensitized solar cells. It has a low cost of fabrication, and is environmentally friendly, among its' advantages [6]. The basic structure of the dye sensitized solar cell (DSSC) consists of a photoanode and a cathode in between which is a redox electrolyte [6, 7]. The cathode is made of Platinum, while the anode is made of mesoporous Titanium dioxide. Both Platinum and Titanium dioxide are separately deposited on Fluorine doped Tin Oxide (FTO) glass substrate. Titanium is given a sense of light by loading it with a dye [8]. When illuminated, electrons in the dye immediately move from the highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO), and subsequently releases electrons into the conduction band of Titanium dioxide [8, 9]. A redox electrolyte restores the dye back to its original state by donating an electron to the dye. The redox electrolyte is itself restored to its original state, once it receives the electron that was injected in the condition band of Titanium. The use of Platinum at the cathode is to catalyze the transfer of electrons from the external circuit to the redox couple. However, the main disadvantage of the dye sensitized solar cell is their low efficiency. A lot of efforts have been made towards improvement of their efficiency [10]. Some of the areas that have been looked at include; increasing the absorption of light by the solar cells within the electromagnetic spectrum, increasing the distance covered by light through multiple reflection in the photoanode, and many more [11]. As a result, there has been significant increase in efficiency of DSSC, achieving 14.1 % by 2017 [12] for DSSC based on ruthenium-based complexes. However, the ruthenium-based dye solar cells are expensive and secondly, ruthenium metals used in making the dyes are scarce [13]. One the other hand, dyes from natural plants are relatively cheap and are in abundancy. Because of the comparative advantages of natural dyes over the ruthenium-based dyes, there has been numerous researches involving naturals dyes, the world over. Natural dyes contain light absorbing pigments. The dyes can be extracted from plant leaves, fruits, flowers and stems. The compounds responsible for light absorption in the pigments are anthocyanins, chlorophyll, betalines and many more. These have been variously explored for application in dye sensitized solar cells [1, 11, 14, 15, 16]. Radin studied dye solar cells fabricated using dye extracts from fresh fruits which included; blueberry, blackrasberry, cherry,cranberry, raspberry, strawberry, red grape [17]. The choice of the fruits was based on their total anthocyanins contents. The dyes were extracted using water as solvent. The highest efficiency obtained was 0.17%. Compared to other dyes in the study, this high performance of the dye was attributed to the short distance between the anthocyanin, cyanidin skeleton and the point of attachment to the TiO2 surface. The short distance facilitates more efficient charge transfer to the anode. In another study, Wuletaw and Delele studied dye solar cells using dye extracts from flowers of Acanthus sennii chiovenda and Euphorbia cotinifolia [14]. The solar conversion efficiency of the solar cells obtained were 0.15% and 0.136% respectively. The 0.15% efficiency was for a solar cell sensitized using ethanol acidified with 1% HCl. Torchani and colleagues, investigated the performance of dye solar cells using dye extracts from Henna and Mallow. Dye solar cells sensitized using extracts from Mallow had a solar conversion efficiency of 0.215%. Henna based solar cell had a solar conversion efficiency of 0.157% [18]. In addition, Abebe and colleagues used dye extracts from Teclea shimperi fruits as sensitizers. The dyes were extracted using different solvents which included water, acidified methanol, acidified ethanol, and acidified water-ethanol mixture at room temperature. The solar cell structure consisted of PEDOT coated FTO counter, TiO2 based anode, and a qusi-solide state electrolyte. Solar cells sensitized using dyes extracted using acidified ethanol produced the best efficiency of 0.3400.012%. Raja and co-workers explored the use of dye extracts from Opuntia dillenii and Tamarindus indica [4]. The dyes were extracted using methanol acidified with 1% HCl. Betalain was extracted from Opuntia dilleniid and anthocyanins were extracted from Tamarindus indica. The betalain based solar cell had efficiency of 0.47%. Anthocyanins sensitized solar, had an efficiency of 0.14%. The mixture of anthocyanins and betalain in ratio 1:1 by volume produced the best efficiency of 0.2%. While it is clear that the solar conversion efficiency of solar cells based on natural dyes are very low, we do hypothesize that, the differences in performance are due to variations in concentration of light absorbing compounds in the dyes. The differences in concentration do influence electron transport in different ways, and the result is the differences in solar conversion efficiency. Dye sensitized solar cells were fabricated based on anthocyanins as sensitizer at varying concentrations. Electron transport was studied using EIS. Electron transport parameters were then used to explain solar cell performances. It was observed that, solar cell performance improves with increase in concentration of anthocyanins. The highest efficiency obtained was 0.145% with concentration of 1.18 mg/ml. EIS studies revealed that, the improvement in solar cell performance was due to increase in recombination resistance at the anode as concentration of anthocyanins increases.

Experimental part

Materials

Methanol, ethyl acetate, acetone,2-propanol, trifluoracetic acid, were purchased locally and were of HPLC grade. Liquid electrolyte (Iodolyte AN-50), platinum catalyst paste (plastisol T/SP), Fluorine doped (FTO) oxide glass substrate (7Ω2), hot melt sealing film meltonix (60μm) were purchased from Solaronix SA. Kerocyanin chloride, liquid detergent, Helmanex III, TiO2 nano powder (Degussa P25) comprising of approximately 30% rutile, and 70% anatase, Triton X-100, glass wool and polyethylene glycol (M.W 10,000) were purchased from Merck.

Materials preparation and anthocyanins extraction

Fresh flowers of Acanthus pubscens were collected from Matugga along Bombo road side, in Wakiso district, in central Uganda. Confirmation of the plant type was done at Makerere University Herbarium in the department of Plant Science, Microbiology and Biotechnology. Fresh flowers (g) of Acanthus pubscens were macerated in methanol (ml) acidified with % trifluoracetic acid for 24 hours. The soaked flowers were sieved and filtered with a funnel fitted with glass wool to obtain ml of crude extract. The filtrate was concentrated using a rotary evaporator set at 30 °C to obtain 40mls. The reason for concentration was to expel methanol, a polar solvent that cannot be partitioned against ethyl acetate [19]. 40 mls were partitioned against ethyl acetate in a separating funnel. The lower layer contained mainly anthocyanins, while the upper layer contained mainly chlorophylls, flavanols, carotenes and polyphenols [20]. The two layers were separated using a separating funnel, and the upper layer discarded. Excess ethyl acetate in the aqueous layer was expelled by subjecting the sample to rotary evaporation for a short time again, and 27mls was recovered. ml of the concentrated sample was divided and transferred into four amber bottles, each carrying 5mls. The amber bottles helped to protect the anthocyanins from light degradation. To each of the four samples was added 20mls, 35mls, 50mls and 65mls of methanol acidified with 0.5% trifluoracetic acid.

Preparation of calibration curve

The major anthocyanin in Acanthus pubscene is cyanidin rutinoside [21]. To determine the concentration of anthocyanins in the dye samples, Kercyanin Chloride standard was used. 0.114 mg, 0.226 mg, 0.329 mg, 0.467 mg and 0.569 mg of Kercyanin Chloride was measured using an electronic balance. The different masses were each dissolved in 10ml of deionized water. Their absorbance was determined at 530 nm using a Jenway spectrophotometer (Model 7305, UK).

Preparation of electrodes

FTO glass substrates were dipped in a bath of helmanex III (1%) for 20 min in an ultrasonic bath and later rinsed three times with deionized water. Finally, the electrodes were bathed in ultra-sonic bath of acetone for 20 min and 2-propanol for 20 min. Titanium paste was prepared by blending 4g of commercial TiO2 nanopowder, 8ml of 0.1M nitric acid solution and polyethylene glycol and Triton X-100. The mixture was completely ground in porcelain mortar to form a paste [15]. The prepared TiO2 paste was deposited by slot coating [14]. Deposition was on the conducting side of the FTO glass substrate, on an of area 36 mm2, defined by a scorch tape. The deposited TiO2 was annealed at 450 °C in an open-air tube furnace (Labtech, model LEEF-4025-3) for 20 min. When it had cooled to about 30 °C, the anodes were dipped in anthocyanins at varying concentrations and left to absorb the anthocyanins for 16 hours. The cathode was prepared by coating FTO glass substrates with a Platinum. An art brush was dipped in plastisol, a platinum precursor and applied onto the FTO glass substrate. Platinum catalyst was activated by annealing in the tube furnace for 20 min. The counter electrodes were left to cool naturally in air.

Assembly of solar cells

The anodes, loaded with the dyes were picked from their holders and washed with ethanol. The anodes were placed with conducting side facing up. Meltonix, cut with a hole of about 8mm by 8mm was placed such that, the deposited TiO2 loaded with the dye was within the hole. The prepared counter electrode, was placed on top of the anode such that, contacts to the solar cells were sufficient for applying copper tape to improve electrical contact, and connecting crocodile clips. Sealing was done by use of a hot solder iron, pressed ontop of the counter electrode, along the edges of the solar cell. The electrolyte, Iodolyte-AN 50 was injected into two holes behind the counter electrode, and the holes sealed with cell cups and meltonix as before.

Measurement of photovoltaic performance and electron transport

Using a solar simulator, intensity of light was set at 1000Wm-2. A Keithley instrument (Model 2400,4066884, C32) was used to measure open circuit voltage, short circuit current, fill factor. Electrochemical impedance spectroscopy (EIS) was done using an Autolab PGSTAT 204. A voltage of 0.7V was applied to the solar cells, and frequency was set to vary from 1Hz to 1MHz.

Results and discussion

Calibration curve and absorption properties of anthocyanins

The absorbance values of standard solutions at varying concentrations were measured at 530 nm.Absorbance was plotted against concentration (Figure 1) using matlab software.
Figure 1

Absorbance-concentration curve for the Kercyanin Chloride standard solutions. The equation inset relates absorbance to concentration. y: Absorbance; x: concentration (mg/ml).

Absorbance-concentration curve for the Kercyanin Chloride standard solutions. The equation inset relates absorbance to concentration. y: Absorbance; x: concentration (mg/ml). As predicted by the Lambert-Bear law, there is a linear relationship between absorbance and concentration [16]. Absorbance of anthocyanins were now measured at 530 nm together with their spectra. The results were plotted using matlab as before, and the spectra is presented in Figure 2.
Figure 2

UV-vis spectra for dyes at varying concentrations; a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. The arrow represents absorbance picks for the different concentrations at 530 nm.

UV-vis spectra for dyes at varying concentrations; a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. The arrow represents absorbance picks for the different concentrations at 530 nm. Using the equation , absorbance values were used to compute concentration of the dye samples. These were; a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. From the UV-vis spectra, Figure 2, all the absorbances peak at approximately 530 nm. This is consistent with results obtained by Namukobe (2006). In an acidic medium, dye extracts with mainly anthocyanins are known to have absorbance peaks at 530 nm [22]. This indicates that, the dye extracts contains mainly anthocyanins. In addition, as concentration increases, the area under the spectra increases. This means the dye is able to absorb more photons as concentration increases. Furthermore, at 530 nm, the peaks increase with concentration. This observation is consistent with the Lambert-Bear law, a linear relationship between absorbance and concentration for a given pathlength of light [16].

Photovoltaic performance

Performance parameters, namely; open circuit voltage (Voc), short circuit current (Isc), and fill factor (FF), were measured. Conversion efficiency (η) was computed using the relation; ; where, is current density, is the power of light incident onto the solar cells [23]. The results are presented in Figure 3 and Table 1.
Figure 3

Current-Voltage (I–V) curves for the dye sensitized solar cells showing the influence of anthocyanins on solar cell performance at 1 sun. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml.

Table 1

Performance of the DSSC with varying concentrations of anthocyanins, measured at 1 sun. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. Voc (V): open circuit voltage; Isc(mA/cm2): short circuit current density; FF: fill factor; η (%): solar conversion efficiency.

Concentration (mg/ml)Voc(V)Isc(mA/cm2)FFη (%)
d0.4685.3330.5820.145
c0.4655.2240.5770.140
b0.4245.0280.5240.111
a0.3805.7780.6200.065
Current-Voltage (I–V) curves for the dye sensitized solar cells showing the influence of anthocyanins on solar cell performance at 1 sun. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. Performance of the DSSC with varying concentrations of anthocyanins, measured at 1 sun. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d:1.18 mg/ml. Voc (V): open circuit voltage; Isc(mA/cm2): short circuit current density; FF: fill factor; η (%): solar conversion efficiency. Table 1 shows that except for the solar cell for which concentration of anthocyanins was lowest; a:0.4 mg/ml, open circuit voltage, short circuit density, fill factor and efficiency all increase with increase in concentration of anthocyanins. Maximum efficiency of 0.145% is obtained at maximum concentration, d. The corresponding; open circuit voltage is 0.468V, short circuit current density:5.333 mA/cm2, and fill factor: 0.582. Increase in fill factor is observed to be marginal, becoming better at higher concentration. The marginal increase is probably due to marginal increase in short current density. Table 2 is a summary of selected studies done on solar cells using natural dyes and an N3 synthetic dye.
Table 2

Summary of performance of selected dyes. Voc(V):open circuit voltage; Isc(mA/cm2): short circuit current density; FF: fill factor; η (%): efficiency.

SpecimenMajor compound presentVoc(V)Isc (mA/cm2)FFη (%)Reference
Acanthus pubscensAnthocyanin (Cyanidin)0.4685.3330.5820.145This work
Acanthus senii chioNot known0.5070.4910.6040.150[14]
BlueberryAnthocyanin (Cyanidin)0.3920.960.470.17[17]
Canarium odontophyllumAnthocyanin (Cyanidin)0.359.740.5461.43[24]
Canarium OdontophyllumAnthocyanin (Pelargonidin)0.3576.570.4840.87[24]
Opuntia dilleniiBetalain0.5211.090.690.47[4]
Tamarindus indicaAnthocyanin0.5320.350.670.14[4]
Red frangipani flowersNot known0.4950.940.650.301[25]
-N3 dye0.7828.310.624.05[25]
Summary of performance of selected dyes. Voc(V):open circuit voltage; Isc(mA/cm2): short circuit current density; FF: fill factor; η (%): efficiency. Performances in Table 2 shows that, dye sensitized solar cells based on natural dyes are generally low. In the table, the highest efficiency of a dye sensitized solar cell based on a natural dye is 0.301%. For N3 dye, which is a synthetic dye, the conversion efficiency is 4.05%. The poor performance of solar cells based on natural dyes have been attributed to probably poor interaction of natural dyes with TiO2 surface.

Discussion of increase in solar cell performance

The increase in short current density as concentration increases can be attributed to increased absorption of light [26]. The increased absorbance of photons leads to increased photogenerated electrons (charge density) resulting into more current. Open circuit voltage increases because of a shift in Fermi level of electrons in the conduction band of TiO2 [27]. To explain the shift in Fermi level of electrons in the conduction band, we consider the definition of open circuit voltage given by Eq. (1) [28].where; is the Fermi level of electrons in the conduction band of TiO2, is the electron charge, is the Boltzmann constant, is temperature of the semiconductor material (TiO2), is the density of states, is the number of electrons injected in the conduction band of the conduction band of TiO2 and is the redox potential of the electrolyte. The first two terms on the right-hand side of Eq. (1) is collectively called the quasi Fermi level of electrons in the conduction band of TiO2. This quasi Fermi level is influenced by the number of electrons, injected into the conduction band of TiO2 [28]. Because is always less than , when becomes large at high concentration of anthocyanins, the term approaches zero. The open circuit voltage is then approximated by Eq. (2) [29]. There is a difference of the term between Equation 1 and Equation 2. The difference is the shift in Fermi level of electrons in the conduction band of TiO2 that results into increase in open circuit voltage. Eq. (2) also gives the maximum possible open circuit voltage that can obtained from a dye sensitized solar cell. However, owing to recombination losses, the open circuit voltage obtained is always low [17, 27]. Other factors which affect the quasi Fermi level include; (1) the number of anchoring groups that attached themselves to TiO2 surface and, (2) type of anchoring group [30]. Anthocyanins extracted from Acanthus Pubscens contains two types of anthocyanins, namely; Cyanidin -3-rutinoside (3%) and Cyanidin-3-glucoside (97%) [21]. The structures are shown in Figure 4.
Figure 4

a Schematic representation of chemical structure of Cyanidin-3-glucoside and b Scheme of Cyanidin-3-rutinoside [21].

a Schematic representation of chemical structure of Cyanidin-3-glucoside and b Scheme of Cyanidin-3-rutinoside [21]. The attachment of cyanidin 3-glucoside onto the semiconductor TiO2 surface is shown in Figure 5.
Figure 5

Schematic representation of complexation between cyanidin and TiO2 surface; a: flavilium form of the anthocyanins; b:quinonoidal form; Glu:glucoside or rutinoside (Adapted from [13] under creative commons licenses [31]).

Schematic representation of complexation between cyanidin and TiO2 surface; a: flavilium form of the anthocyanins; b:quinonoidal form; Glu:glucoside or rutinoside (Adapted from [13] under creative commons licenses [31]). The mode of attachment is through bidentate. The adsorption of the dye onto the semiconductor surface acts as a pathway for injecting electrons into the conduction band of TiO2 [13]. The interaction of these two types of anthocyanins with TiO2 too probably causes a shift in the Fermi level of electrons in the conduction band [13, 27]. The saturation of short circuit current as well as open circuit voltage as observed from the closeness of I–V curves as concentration increases can be attributed to decrease in electron injection efficiency into the conduction band of TiO2 as a result of shift in the conduction band, the nature of materials used to construct the solar cells [27] and steric hinderance on the surface of TiO2 as the concentration of anthocyanins increase [32]. The steric hindrance affects the attachment of dye molecules on the TiO2 surface and therefore not only affects charge injection in the conduction band of TiO2 [8,17], but also the Fermi level of electrons in TiO2. Both fill factor and solar conversion efficiency are functions of short circuit current and open circuit voltage. Their variations are there for influenced by changes in open circuit voltage and short circuit current.

Electrochemical impedance spectroscopy

Information about electron transport in the solar cells was investigated using impedance spectroscopy. Figure 6 shows the impedance spectra that was obtained.
Figure 6

Nyquist plot, a graph of imaginary impedance against real impedance for the solar cells at varying concentrations. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d: 1.18 mg/ml.

Nyquist plot, a graph of imaginary impedance against real impedance for the solar cells at varying concentrations. a:0.4 mg/ml; b:0.6 mg/ml; c:1.0 mg/ml; and d: 1.18 mg/ml. Interpretation of the EIS spectra was done in line with the transmission line model [33]. Figure 7 was proposed as the equivalent circuit for the solar cell, and was used to interprete the EIS spectra.
Figure 7

Simplified transmission line model; R1: Series resistance; R2: recombination resistance of counter electrode; R3: recombination resistance of anode; C1: chemical capacitance of anode; C2: Helmholtz capacitance of counter electrode; W: Warburg impendance.

Simplified transmission line model; R1: Series resistance; R2: recombination resistance of counter electrode; R3: recombination resistance of anode; C1: chemical capacitance of anode; C2: Helmholtz capacitance of counter electrode; W: Warburg impendance. Usually, the impedance spectra consist of three arcs [34]. The visibility of the arcs depends on the applied biasing voltage to the solar cell [33]. At some applied voltages, depending on the solar cell, the arcs may overlap one another [35]. In Figure 6, the clearly visible arc is associated with a parallel combination of resistance to recombination, R3 at the anode, and the chemical capacitance C2 of the anode. The diameter of this arc equals R3 [36]. This was measured using EIS spectrum analyzer [37]. The measurement is illustrated on Figure 6 [36, 38]. R1 is read from the first intercept on the real axis. Transport resistance was computed through the relation; R1+ R2+ R3 [39]. R2 was set to zero because of absence of arcs representing recombination at the counter electrode in Figure 6. The measured and computed parameters are presented in Table 3.
Table 3

Determined electron transport parameters from Nyquist plots. a: 0.4 mg/ml; b: 0.6 mg/ml; c: 1.0 mg/ml; and d: 1.18 mg/ml; R1: series resistance, R3; recombination resistance at anode : transport resistance.

Concentration of dye used (mg/ml)R1(Ω)R3(Ω)Rt(Ω)
d13.02200.15213.17
c12.41120.19132.60
b13.7781.2094.97
a17.5153.8371.34
Determined electron transport parameters from Nyquist plots. a: 0.4 mg/ml; b: 0.6 mg/ml; c: 1.0 mg/ml; and d: 1.18 mg/ml; R1: series resistance, R3; recombination resistance at anode : transport resistance. It follows from Table 3, that the solar cell with the lowest concentration has the lowest recombination resistance and lowest transport resistance. The solar cell with the highest recombination resistance and transport resistance is made from the highest concentration of anthocyanins. Thus, recombination resistance and transport resistance is observed to increase with increasing concentration of anthocyanins. The recombination resistance is defined by Eq. (3) [29].where; is the current that results from recombination, is the applied voltage corrected for series resistance, is a coefficient that is related to non-ideality factor, through . It defines the loss of charge from TiO2 to electrolyte. is the electron charge, is Boltzmann constant, and is a parameter which defines activation of recombination. It is defined by Eq. (4)where; is the thickness of TiO2, is the concentration of acceptor species in TiO2, reorganization energy of acceptor species, is a parameter associated with electron traps below the conduction band of TiO2, is the rate constant for recombination kinetics. It follows from Eqs. (3) and (4) that, it is R0 which influences recombination resistance, R3 [40]. We note that, R0 is its self a function of rate constant for recombination kinetics, , the energy difference, , and many other parameters defined in Eq. (4). In a solar cell, all the other parameters are constant except and which depend mostly on the number of electrons injected in the conduction band of TiO2 [27]. Thus, the increase in recombination resistance can be attributed to increase in R0, which is directly linked to the number of electrons injected in the conduction band of TiO2 [29]. It is possible that, increase in recombination resistance leads to increased electron lifetime, and therefore fewer elections do recombine with electron acceptor species [41].

Conclusion

Dye sensitized solar cells were fabricated and sensitized using anthocyanins at different concentrations. The concentration of the anthocyanins used were 1.18 mg/ml, 1.00 mg/ml,0.60 mg/ml and 0.40 mg/ml. The solar cells had conversion efficiencies of 0.145%, 0.140%, 0.111% and 0.065% respectively. It was observed that open circuit current density, open circuit voltage, fill factor and solar conversion increase with increase in concentration of anthocyanins. The increase in concentration allows for absorption of more light, and more electrons are exited and injected into the conduction band of TiO2. This avails more charge for transportation to the solar cell contacts. The increase in charge density is indicated by increase in short current density. The increase in open circuit voltage was attributed to shift in Fermi level of electrons in the conduction band of TiO2. The Fermi level begins to shift immediately charge density begins to increase. The shift in Fermi level also led to increase in recombination resistance. The bigger recombination resistance as concentration increased, probably led to longer electron lifetime since fewer electrons recombined with electron acceptor species. More electrons were therefore collected and transported to cell contacts.

Declarations

Author contribution statement

Alex Okello: Conceived and designed the experiments; Performed the experiments; Analyzed and interpreted the data; Wrote the paper. Brian Owino Owuor: Conceived and designed the experiments; Performed the experiments. Jane Namukobe: Conceived and designed the experiments; Analyzed and interpreted the data. Denis Okello: Analyzed and interpreted the data. Julius Mwabora: Analyzed and interpreted the data.

Funding statement

This work was supported by African Center of Excellency in Materials, Product Development and Nanotechnology (MAPRONANO-ACE), Uganda (003) at Makerere University and International Science Program (ISP) of Sweden, UG 001 project under Materials Science and Solar Energy Network for Eastern and Southern Africa (MSSEESA)

Data availability statement

Data will be made available on request.

Declaration of interests statement

The authors declare no conflict of interest.

Additional information

No additional information is available for this paper.
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