Bulk heterojunction (BHJ) polymer solar cells (PSCs) which are based on conjugated polymer donor and fullerene derivative acceptor materials have attracted much attention due to the efficient charge transfer from conjugated polymers to fullerene derivatives. Compared to inorganic solar cells, Polymer solar cells (PSCs) usually have one important hindrance for the efficiency improvement with insufficient light absorption due to the thin active layer which is restricted by the short exciton diffusion length and low carrier mobility[1-3]. In recent years, tremendous effort has been taken to develop the light absorption of the polymer solar cells and increase the power conversion efficiencies (PCE) of single junction cells and the PCE has exceeded 14% of the single junction solar cells. This development is a result of the tuning of active layer materials with light absorption counterparts, development of the surface morphology of the thin films, reducing the series and shunt resistance of the devices etc. The Regioregularpoly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61-bu-tyric acid methyl ester (PCBM) blend is one of the common and promising materials for achieving high PCE because of the high self-organizing ability, high hole mobility, and broad range absorption in the red region of the electromagnetic spectrum. However, more efficient Sun energy harvesting requires the compounds to absorb strongly in the visible region of the spectrum [4-5].
Illuminated metallic nanoparticles (NPs) such as Au and other metallic nanostructures can be used to enhance the light absorption of the polymer thin films due to the localized surface plasmon resonance (LSPR) effect which enables to a remarkable enhancement of local electromagnetic fields [6,7]. The LSPR of metallic NPs is referred to as the collective oscillation of electrons residing on the metallic NPs are excited by the incident light photons at the resonant frequency . The LSPR excitation of the metallic NPs results the improved electromagnetic fields, light absorption and scattering due to their physical and elemental parameters, which leads enhanced device performances. Considering the strong LSPR effect of the metallic NPs such as Ag and Au, many researchers have been widely investigated them for difference technological applications including photovoltaic device fabrications [9,10]. Brown et al  have shown that the metallic nanostructures in the active layer can scatter the incident photons through a long propagation path resulting a higher light absorption and photocurrent generation of PSCs. Lu et al  reported 20% enhancement of power conversion efficiency of Au and Ag incorporated PSCs due to the LSPR effect.
On the other hand, NPs of transition metal oxides such as copper oxide nanoparticles (CuO NPs) have gained special attention due to the low cost, non-toxic, and high optical absorption capabilities. CuO is a p-type semiconductor with a direct band gap energy of 1.5eV which is close to the ideal energy gap of 1.4eV for fabricating the high optical absorbing solar cells [13–16]. In the previously reported work by the author [17-19] has shown that incorporation of the CuO NPs in the active layer increased the power conversion efficiency (PCE) of the solar cells by 40.6%.
Many previous researches have been done on tuning the polymer solar cells with inorganic nanoparticles (NPs). The inorganic NPs of various sizes and configurations have been integrated into organic solar cell architecture in order to fine tune and enhance the morphology, electronic and optical absorption of respective PSCs. As a result, significant enhancements in the power conversion has been obtained. Depending on the position in the PSC architecture, incorporation of NPs can be categorized into three main groups which are: (i) photoactive or hole transport layers, (ii) buffer layers, and (iii) between different interfaces . Table 1 summarizes the reported electrical parameters of such studies indicating the respective efficiency improvements.
However, there is no reported work for incorporating both Au NPs and CuO NPs in the active layer of PSCs. Therefore, this study will be extended to investigate the effect of the CuO NPs together with Au NPs in the P3HT/PCBM (poly (3-hexylthiophene)/ [6, 6]-phenyl-C70-butyric acid methyl ester) active layer of the polymer solar cell devices. Also, the effect of the Au and CuO NPs on P3HT/ PCBM devices will be demonstrated through the optoelectronic and nano-scale morphology aspects and reveal their influences on PCE of the Solar cells. The optoelectronic and morphological parameters are comparatively studied by UV absorption, SEM, EQE, AFM and solar simulation.
MATERIALS AND METHODS
Poly(3-hexylthiophene) (P3HT) (Rieke Metals), phenyl-C70butyric acid methyl ester (PC70BM) (SES Research), Nanoparticles of gold (Au) (15 nm diameter) and Nanoparticles of CuO (10-30nm diameter) (nanocs.com), Glass substrates measuring 24 x 80 x 1.2 mm (12 Ω/cm2) with an Indium Tin Oxide (ITO) conductive layer of 25-100 nm (nanocs.com) and Aluminium coils with a diameter of 0.15 mm (Ted-Pella, Inc.) were used as received. poly(3,4ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT/PSS) mixed in distilled water was obtained from Sigma Aldrich and it was mixed with an equal amount of distilled water. All processing and characterization work of the PSC devices were conducted under the same experimental conditions.
The conductive glass substrates were ultrasonically cleaned with ammonium hydroxide, hydrogen peroxide, distilled water, methyl alcohol, and isopropyl alcohol; successively. The fabrication of polymer based solar cells containing Au-NPs was carried out in a N2 filled glove box. The P3HT-PC70BM blend was obtained by diluting equal amounts of regioregular P3HT and PC70BM (10 mg each) with 2 ml of chlorobenzene (C6H5Cl) and mixing for 14 hours at 50oC. The next step is the incorporation of Au-NPs (15 nm diameter) and CuO-NPs into the blend by dispersing NPs in 2 ml of chlorobenzene and adding it to the P3HT/PCBM blend in weights leading to be the final weight ratios (P3HT/PCBM/AuNPs/CuO-NPs) of 10:10:0:0; 10:10:0.05:0; 10:10:0:0.6; and 10:10:0.05:0.6 mg, respectively.
The solar cell devices were spun coated in a glove box with N2 atmosphere. A 40 nm-thick PEDOT/PSS layer, which serves as a thin hole-transport layer, was spun coated at a rotational velocity of 4000 rpm, followed by heating at 120°C for 20 minutes in the air. When the temperature of the samples reached the ambient temperature, the blends with P3HT: PC70BM: Au-NPs: CuO NPs solution was spun coated for two minutes at 1000 rpm. The active layers measured 120 nm in average thickness and 0.12 cm2 in surface area. A schematic illustration of the layered structure of the fabricated devices is shown in Fig. 1.
Current density–voltage (J-V) characterization was carried out for all PSCs using a UV solar simulator with an AM 1.5G filter and a lamp intensity of 100 mW/cm2. A source meter (Keithley 2400) was used to obtain the J-V measurements. Device parameters; such as short circuit current (Jsc), open circuit voltage (Voc), fill factor (FF) and power conversion efficiency (PCE) were recorded under ambient conditions. A quantum efficiency measurement kit (Newport-425) embedded in the solar cell simulator was used to obtain EQE values. A PerkinElmer LAMBDA 650 spectrophotometer was used to obtain the optical properties of cells.
An Agilent 5420 atomic force microscope(AFM) was used to analyze the surface morphology. The Pico Image Basics and Gwyddion software were utilized to determine the root mean square roughness (σrms) of the surface under ACAFM non-contact mode with set point 1.60, I-gain of 10, and scanned area of 2x2μm. The layer structures of the fabricated solar cells were analyzed using a scanning electron microscope with an energy dispersive x-ray detector (FEG-SEM Hitachi S-4800).
RESULTS AND DISCUSSION
PSC devices based on four different concentrations of Au and CuO NPs were fabricated and tested under simulated 100 mW cm-2 AM1.5G illumination. Table 2 indicates the photovoltaic parameters, such as Jsc, Voc, fill factor (FF) (equation 1), and PCE (equation 2), of all the fabricated devices.
Where, Pin is the input power.
Summarized data demonstrates that the Voc remained nearly the same for all four types of devices. The Voc is directly related to the energy difference between the LUMOs of donor and acceptor materials which should be larger than 0.3 eV for efficient excitonic dissociation [33, 34]. But, the Voc of organic solar cells is restricted by the difference between the HOMO of the donor and the LUMO of the acceptor. However, the above results imply that the positions of the HOMO of the donor and the LUMO of the acceptor was not altered by Au or CuO NPs in the active layer. In spite of the Voc trend, it is clear that the Jsc increased from 5.338 mA/cm2 to 6.228 mA/cm2 by adding Au NPs in the active layer. The Jsc was further increased from6.228 mA/cm2 to 6.829 mA/cm2 after adding CuO NPs into the P3HT/PCBM active layer. However, the highest Jsc value of 7.218 mA/cm2 was exhibited by the PSCs which are contained both Au and CuO NPs in the active layer. The FF values enhanced from 61% to 66%. However, the FF value remained unchanged at 66% without depending on the type of the NPs. The FF explains the combination of the series resistance (Rs) and shunt resistance (Rsh) of the device. Rs represents the sum of contact resistance on the front/back surfaces and the ohmic resistances. Shunt resistance is mainly due to the imperfections on the device surface . The Au NPs and CuO NPs did not show a significant influence on the resistance of the device. These improved Jsc and FF influenced PCE and it was enhanced from 2.114% to 3.144% by incorporating Au and CuO NPs in the same P3HT/PCBM active layer. This increased in PCE translates to a 48.7% total enhancement of the PCE in comparison to the reference cells. Fig. 2 shows J-V characteristics curves of ITO/PEDOT: PSS/ P3HT /PCBM/Al solar cells with different concentrations of Au NPs and CuO NPs in the P3HT/PCBM active layer.
The Jsc of the solar cell device has a linear relationship with the EQE which is theoretically indicated as equation 3.
where q is the value of the charge, ℏ is the reduced Planck constant, C and λ are the velocity and the wavelength of the light respectively.
The EQE is a ratio between the incident photons on the solar cell from the input light and the generated free charge carriers by the solar cell. The EQE can be modified as internal quantum efficiency (IQE) neglecting reflectance and transmittance of the incident photons to consider only the portion of the absorbed light by the active region. In the organic semiconductor based solar cells, EQE can be determined by five major factors which are composed of inherent efficiency components  which can be shown in equation 4.
Here, ηA, ηdiff, ηdiss, ηtr and ηcc are represented the light absorption efficiency, the excitonic diffusion efficiency, the excitonic dissociation efficiency, the charge transport efficiency, and the electrons-holes collection efficiency respectively.
The shape of the EQE can be used to understand the material properties of the device and it is strongly correlated to the junction thickness and blend composition of the active layer. Furthermore, the shape of the EQE explains the mechanisms for free carrier generation in the active layer region. To confirm the accuracy of the J-V measurements, the EQE spectrum of the devices which were fabricated using four different concentrations of Au and CuO NPs was measured. The EQE curves are shown in Fig. 3. Corresponding EQE spectra for solar cells are improved from 45% to 68.5%. These all the devices exhibit efficient photoconversion in the range of 400–750 nm. To obtain such higher EQE values, it is requisite to accomplish enhanced and efficient light absorption, exciton diffusion, charge carrier separation, and charge collection at the electrodes. Therefore, this improved EQE conduct to better elucidate improved Jsc relevant to the enhanced free carrier generation.
The metal nanostructures exhibit one of the most important properties is plasmonic behavior which is the collective oscillation of free electrons in the metal structure. Other properties of metal nanostructures such as reflection and transmission occur when the frequency of the incident light is below the plasma frequency and above the plasma frequency respectively. Frequently, the range of the plasma frequency of metals is in the ultraviolet domain, which leads to plasma reﬂective in the visible range. The plasmonic energy of such structures can be written as equations 5 and 6.
where n is the electron density, e is the electron charge, m is the electron mass, is the permittivity of the free space, is the Planck constant, and is the plasmon frequency.
On the other hand, surface plasmons related to a metallic nanoparticle can be considered as localized surface plasmons (LSPs). When the light shines on the metallic nanoparticles, the electrons associated with the surface of the NPs are subjected to collective oscillate called LSPs as shown in Fig. 4. In addition, the Mie solution to Maxwell’s equations for the spherical nanoparticles explains the scattering and absorption phenomena of the incident light. The correlation of the absorption cross-section ( and the scattering cross-section (σsc) of the metal nanoparticles to the extinction cross-section ( can be shown in equation 7 [36, 37].
This plasmonic behavior of the Au NPs is a crucial factor of increasing the light absorption in the fabricated polymer solar cells in this study. Photo-absorption and carrier generating ability of a polymer thin film are represented by the photon absorption (ηA) efficiency as shown in equation 4. Also, the light absorption of a semiconductor thin film is controlled by the energy band structure, absorption coefficient, and the thickness of the photoactive layer [38, 39]. On the other hand, the CuO NPs can be considered as the P3HT tuning materials due to their suitable energy band structure and photo-electrons donor properties. Therefore, CuO NPs may increase the exciton generation and dissociation process in the PSCs. Also, CuO NPs play a role being charge hopping centers for charge carriers enabling high charge mobility within the structure. N.R. Dhineshbabu et al  reported that the CuO NPs have shown high optical absorbance at UV region, and then it decreases exponentially in the visible region near the IR region.
So the CuONPs are very high absorptive at the UV region and they are more convenient for the fabrication of the solar cells. Also, the CuO thin film has a high optical absorption coefficient which is conducive to increase the probability of direct transition occurrence. On the other hand, the CuO nanoparticles consist of small nanocrystalline clusters with different orientation of the single crystal diffraction pattern and, the CuO nanoparticles encourage the formation of P3HT crystallites reducing the charge carrier diffusion length. Therefore, these CuO NPs clusters and crystallized P3HT enhance the charge carrier hopping process minimizing the charge recombination. These inherent composites inherent properties of the Au and CuO NPs were used to enhance the light absorption of the P3HT/PCBM solar cells. The UV-vis absorption This reduced bandgap is encouraged the smooth transition of the free electrons from the donor material to the acceptor material. The UV-vis absorption, EQE, and Jsc measurements were significantly increased showing the same trend. Therefore, it can be identified that the plasmonic effect (LSPR) of Au NPs and absorption properties of CuO NPs play a significant role in enhanced PCE of the solar cell devices.
The AFM images of the P3HT/PCBM with different concentrations of Au and CuO NPs dispersed ﬁlms were obtained to understand the surface morphology of the active layer as shown in fig. 6. Significantly different morphologies were observed for these four types of devices in their AFM images. The root-mean-square roughness (Rrms) is linearly correlated with the interfacial surface area between the active layer and PEDOT: PSS hole collection layer or Al cathode. The increase of the interfacial surface area leads to the efficient dissociation of excitons into holes and electrons. The P3HT/PCBM layer showed a relatively smooth surface with root-mean-square roughness (Rrms) value of 0.10 nm. It was noticed that the Rrms value of the P3HT/PCBM layer was increased with increasing the concentration of the NPs in the P3HT/PCBM blend. The Rrms of the device with 0.05 Au NPs was 0.81 nm. However, it was exhibited 0.32 nm in the samples containing 0.6 mg of CuO NPs. Furthermore, the Rrms value was enhanced up to 0.91nm of the P3HT/PCBM layers incorporated with both CuO and Au NPs as shown in table 3.
This increased surface roughness contributes to enlarge the interfacial contact area between the PEDOT: PSS and P3HT/PCBM-CuO/Au NPs layers, allowing high efﬁcient hole collection at the anode and hence improve the Jsc and shape of the FF. Also, this increased surface roughness of the cells with Au and CuO NPs is evidence of adequate space for P3HT crystallites to form in the active layer structure. Higher P3HT crystals discourage the fully amorphous PCBM molecules to dissolve in the P3HT domain, thus promoting the aggregation of PCBM, which will contribute to better P3HT/PCBM phase separation. The SEM images of the hybrid structure of the fabricated PEDOT: PSS/ P3HT: PCBM/Au-CuO NPs/device are shown in the Fig. 7. The Au and CuO-NPs added the P3HT/PCBM active layer was approximately in the range of 100-160nm thickness. It is helpful to eliminate the charge recombination losses in the devices. The thickness of the PEDOT: PSS hole transport layer was estimated as 40nm.
In this study, Au and CuO-NPs were added to the P3HT/PCBM layer of solar cells in order to increase the power conversion efficiency. The PCE increased from 2.114 to 3.144% in the cells containing 0.05 mg Au-NPs and 0.6mg CuO-NPs, which is equivalent to 48.7% improvement of efficiency. The higher performance is attributed to enhanced UV-vis absorption, EQE and Jsc. The optical absorption spectrum changed significantly after presence of Au-NPs in the P3HT/PCBM active layer due to the strong near field around Au-NPs. EQE of the solar cells increased due to the increased hole and electron polaron mobilities in cells with Au and CuO NPs. AFM analysis showed an increase in surface roughness of the P3HT/PCBM active layer with Au and CuO NPs, which is an indication of larger space to form the P3HT crystallites. Also, the FF was enhanced by adding these Au and CuO NPs in the cells, but it was a constant value with different concentrations of the NPs.
CONFLICT OF INTEREST
The authors declare that there are no conflicts of interest regarding the publication of this manuscript.