Hybrid inverted organic photovoltaic cells based on nanoporous TiO2 films and organic small molecules

Solar cells based on nanoporous TiO₂ films with an inverted structure of indium tin oxide (ITO)/TiO₂/copper phthalocyanine (CuPc):fullerene (C₆₀)/CuPc/poly(3,4-oxyethyleneoxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/Au were fabricated. The best overall photovoltaic performance undergoing a series of device optimization was achieved with the device of ITO/dense TiO₂ (30 nm)/nanoporous TiO₂ (130 nm)/C₆₀:CuPc (1:6 weight) (20 nm)/CuPc (20 nm)/PEDOT:PSS (50 nm)/Au (30 nm). The device using the nanoporous TiO₂ films has better photovoltaic properties compared to those using dense TiO₂ films. Higher photovoltaic performances were obtained by introducing a coevaporated layer of C₆₀:CuPc between TiO₂ and CuPc. The stability of inverted structure was better than that of the normal device, which gives a promising way for fabrication of solar cells with improved stability.     

Efficiency enhancement of polymer solar cells by incorporating a self-assembled layer of silver nanodisks

We report the efficiency enhancement of polymer solar cells by incorporating a silver nanodisks' self-assembled layer, which was grown on the indium tin oxide (ITO) surface by the electrostatic interaction between the silver particles and modified ITO. Polymer solar cells with a structure of ITO (with silver nanodisks)/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) (Clevious P VP AI 4083)/poly(3-hexylthiophene):[6,6]-phenyl-C61 butyric acid methyl ester (P3HT:PC₆₁BM)/LiF/Al exhibited an open circuit voltage (V_OC) of 0.61±0.01 V, short-circuit current density (J_SC) of 9.24±0.09 mA/cm², a fill factor (FF) of 0.60±0.01, and power conversion efficiency (PCE) of 3.46±0.07% under one sun of simulated air mass 1.5 global (AM1.5G) irradiation (100 mW/cm²). The PCE was increased from 2.72±0.08% of the devices without silver nanodisks to 3.46±0.07%, mainly from the improved photocurrent density as a result of the excited localized surface plasmon resonance (LSPR) induced by the silver nanodisks.     

Organic solar cells with 2-Thenylmercaptan/AU self-assembly film as buffer layer

The interface between an electrode and the organic active layer is an important factor in organic solar cells (OSCs) that influences the power conversion efficiency (PCE). In this report, a buffer layer of 2-thenylmercaptan/Au self-assembly film is introduced into OSCs as a substitute for the poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT: PSS) layer. The electrode/active layer interface is meliorated by Au-S coordinate bond of self assembly after applying this buffer layer. The series resistance reduces from 20 Ω cm² in a device based on PEDOT:PSS to 10.2 Ω cm². Correspondingly, the fill factor (FF) increases from 0.50 to 0.64. Moreover, due to the dipole of this self-assembled layer, the open circuit voltage (V_oc) also increases slightly from 0.54 V to 0.56 V and the PCE reaches 2.5%.     

Mechanical flexibility of transparent PEDOT:PSS electrodes prepared by gravure printing for flexible organic solar cells

The mechanical flexibility of transparent poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) films printed onto a flexible PET substrate using a gravure printing method was investigated using a lab-made bending test system. Gravure-printed PEDOT:PSS electrodes with a sheet resistance of 359 Ω/square and a transparency of 88.92% showed outstanding flexibility in several types of flexibility tests, including outer/inner bending, twisting and stretching. Notably, the PEDOT:PSS electrode had a constant resistance change (ΔR/R₀) within an outer and inner bending radius of 10 mm. In addition the stretched PEDOT:PSS electrode showed a fairly constant resistance change (ΔR/R₀) up to 4%, which is more stable than the resistance change of conventional amorphous ITO electrode. The twisting test revealed that the resistance of the PEDOT:PSS electrode began to increase at an angle of 36° due to delamination of the film from the PET substrate. Despite the high sheet resistance of the PEDOT:PSS electrode the flexible organic solar cells fabricated on the PEDOT:PSS electrode showed a power conversion efficiency of ∼2% (FF: 44.9%, V_o: 0.495 V and J_sc: 9.1 mA/cm²), indicating the possibility of using gravure printed PEDOT:PSS as a flexible and transparent electrode for printing-based flexible organic solar cells.     

Glass/ITO/In(O,S)/CuIn(S,Se)2 solar cell with conductive polymer window layer

Hybrid solar cells based on the combination of conductive polymer poly(3,4-ethylenedioxythiophene) (PEDOT) doped with polystyrenesulfonate (PSS) and inorganic semiconductor CuIn(S,Se)₂ (CISSe) were investigated. The CuInSe₂ (CISe) absorber layers were electrodeposited on ITO covered glasses from aqueous solutions with various ratios of elements. The ITO/In(O,S)/CISSe photovoltaic (PV) junctions were prepared by the sulfurization of ITO/CISe precursors at 450 °C in the H₂S atmosphere.The PEDOT–PSS layer of p-type is considered an alternative to the traditional window top layer on the CISSe absorber layer in the cell structure. The polymer deposition was performed by help of the spin-casting technique. PV properties of the prepared ITO/In(O,S)/CISSe and ITO/In(O,S)/CISSe/PEDOT–PSS structures were studied, with emphasis on the role of conductive polymer layer in the cell structure.     

Morphological and electrical effect of an ultrathin iridium oxide hole extraction layer on P3HT:PCBM bulk-heterojunction solar cells

An ultrathin iridium layer was treated with O₂-plasma to form an iridium oxide (IrO_x), employed as a hole extraction layer in order to replace poly(3,4-ethylenedioxythiophene):poly(styrene-sulfonate) (PEDOT:PSS) in organic photovoltaic (OPV) cells with poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM). The IrO_x layer affects the self-organization of the P3HT:PCBM photo-active layer due to its hydrophobic nature, inducing a well-organized intraplane structure with lamellae oriented normal to the substrate. Synchrotron radiation photoelectron spectroscopy results showed that the work function increased by 0.57 eV as the Ir layer on ITO changed to IrO_x by the O₂-plasma treatment. The OPV cell with IrO_x (2.0 nm) exhibits increased power conversion efficiency as high as 3.5% under 100 mW cm⁻² illumination with an air mass (AM 1.5G) condition, higher than that of 3.3% with PEDOT:PSS.     

Highly durable inverted-type organic solar cell using amorphous titanium oxide as electron collection electrode inserted between ITO and organic layer

An indium tin oxide/titanium oxide/[6,6]-phenyl C₆₁ butyric acid methyl ester:regioregular poly(3-hexylthiophene)/poly(3,4-ethylenedioxylenethiophene):poly(4-styrene sulfonic acid)/Au type organic solar cell (ITO/TiO_x/PCBM:P3HT/PEDOT:PSS/Au) with 1 cm² active area, which is called “inverted-type solar cell”, was developed using an ITO/amorphous titanium oxide (TiO_x) electrode prepared by a sol-gel technique instead of a low functional electrode such as Al. The power conversion efficiency (η) of 2.47% was obtained by irradiating AM 1.5G-100 mW cm⁻² simulated sunlight. We found that a photoconduction of TiO_x by irradiating UV light containing slightly in the simulated sunlight was required to drive this solar cell. The device durability in an ambient atmosphere was maintained for more than 20 h under continuous light irradiation. Further, when the air-stable device was covered by a glass plate with a water getter sheet which was coated by an epoxy-UV resin as sealing material, the durability was still higher and over 96% of relative efficiency was observed even after continuous light irradiation for 120 h.     

Efficient hole collection by introducing ultra-thin UV-ozone treated Au in polymer solar cells

Efficient hole collection in polymer solar cells (PSCs) has been achieved by introducing an ultra-thin UV-ozone (UVO) treated Au on indium tin oxide (ITO) to substitute poly-(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). Through optimizing the Au thickness and the duration of UVO treatment, it is shown that the ITO/Au (1 nm) treated by UVO for 15 s improves the fill factor significantly to 67.2% and power conversion efficiency (PCE) to 3.47%, which is competitive to that of the PEDOT:PSS-based PSCs with PCE of 3.38%. The results of ultraviolet photoemission spectroscopy and the analysis of the current conduction mechanism show that the UVO-treated Au offers favorable band alignment at metal/polymer interface of the anode for efficient hole collection. Meanwhile, the series resistance of the device decreases drastically.     

Enhancing the short-circuit current and efficiency of organic solar cells using MoO3 and CuPc as buffer layers

Efficient bulk-heterojunction (BHJ) (regioregular poly (3-hexylthiophene) (P3HT): (6, 6)-phenyl C₆₁ butyric acid methyl ester (PCBM)) solar cells were fabricated with molybdenum trioxide (MoO₃) and copper phthalocyanine (CuPc) as buffer layers. The insertion of MoO₃ layer was found to be critical to the device performance, effectively extracting holes to prevent the exciton quenching and reducing the interfacial resistance because of alignment of energy levels. The introduction of CuPc buffer layer was observed to be ameliorative for device performance, further enlarging the visible absorption spectra range of the devices. The effect of the MoO₃ and CuPc layer thickness on device performance was studied. The optimized thickness was achieved when MoO₃ layer was 12 nm and CuPc layer was 6 nm, resulting in optimized power conversion efficiency (PCE) of 3.76% under AM1.5G 100 mW/cm² illumination.     

Low bandgap carbazole copolymers containing an electron-withdrawing side chain for solar cell applications

A new series of low bandgap carbazole copolymers containing an electron-withdrawing moiety as a side chain, via Suzuki, Yamamoto, and Stille polymerization reactions has been synthesized. Their bandgaps and molecular energy levels can be tuned by copolymerizing with different conjugated electron-donating units. The resulting copolymers have low optical and electrochemical bandgaps. The optical bandgaps of the copolymers range from 1.79 to 1.24 eV. In order to investigate their photovoltaic properties, polymer solar cell devices based on low bandgap copolymers were fabricated with a structure of ITO/PEDOT:PSS/copolymers:PCBM/Al, under the illumination of AM 1.5 G, 100 mW/cm². The power conversion efficiencies (PCE) of the polymer solar cells based on these low bandgap copolymers were measured. The best performance was obtained by using PC-CARB as the electron donor and 6,6-phenyl C₇₁-butyric acid methyl ester (PC₇₁BM) as the electron acceptor. The PCE of the solar cell based on PC-CARB/P₇₁CBM (1:4) was 1.27% with an open-circuit voltage (V_oc) of 0.65 V, and a short-circuit current (J_sc) of 6.69 mA/cm².     

Synthesis and photovoltaic properties of a low bandgap donor-acceptor alternating copolymer with benzothiadiazole unit

A new donor-acceptor alternating copolymer as the donor material of the active layer in polymer solar cells has been synthesized. The alternating structure consisted of dithieno[3,2-b:2′,3′-d]thiophene (DTT) donor unit and 5,6-bis(tetradecyloxy)benzo-2,1,3-thiadiazole (BT) acceptor unit. Both units were confirmed by ¹H NMR and elemental analysis. Since the BT unit has long alkyoxyl side chains, the polymer was soluble in common organic solvents. Optoelectronic properties of the copolymer (PDTTBT) were investigated and observed by UV-vis, photoluminescence (PL) spectra, and cyclic voltammogram (CV). UV-vis spectrum exhibited a broad absorption band in the range of 300-750 nm and a low bandgap of 1.83 eV. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels of PDTTBT could be determined from the data of CV and UV-vis spectrum. Based on the ITO/PEDOT:PSS/PDTTBT:PCBM/Al device structure, the power conversion efficiency (PCE) under the illumination of AM 1.5 (100 mW/cm²) was 0.113%. It was found that PCE of 0.301% could be acquired under the annealing condition at 150 °C for 30 min. In addition, solar cells fabricated with the 1,8-octanedithiol (OT) additive in the mixture solvent or adding TiO_x optical spacer show efficiencies significantly improved over 15%.     

Efficient hybrid carboxylated polythiophene/nanocrystalline TiO2 heterojunction solar cells

Efficient hybrid solar cells fabricated from TiO₂, novel carboxylated polythiophene poly (3-thiophenemalonic acid) P3TMA as sensitizer as well as hole conductor and poly (3-hexylthiophene) (P3HT) as hole transporter was described. UV-Vis absorption and morphology of the active layer were investigated. Device J/V characterizations with different P3HT layer thickness were measured and discussed. Efficiency improvements were observed in thinner P3HT layer thickness and with poly[3,4-(ethylenedioxy)-thiophene]:poly(styrene sulfonate) (PEDOT:PSS) as charge collection layer, and such device showed a short-circuit current density of 1.32 mA/cm², an open-circuit voltage of 0.44 V, a fill factor of 0.43, and a energy conversion efficiency of 0.25% at A.M. 1.5 solar illumination (100 mW/cm²).     

Synthesis and characterization of a novel fullerene derivative for use in organic solar cells

A novel fullerene derivative with an N-hexylphenothiazine moiety, PTZ-C_60, was synthesized and characterized. The new synthesized fullerene showed good solubility in common organic solvents such as toluene, chlorobenzene and 1, 2 dichlorobenzene. The synthetic product PTZ-C₆₀ was characterized by ¹H and ¹³C NMR, FT-IR and UV-vis spectroscopy. Photovoltaic devices were fabricated using the new fullerene derivative as the electron acceptor and P3HT as the electron donor. The configuration of the device was as follows: ITO/PEDOT:PSS/active layer/LiF/Al. The weight ratios of the electron donor to the acceptor in the active layer were 1:0.5, 1:0.7, and 1:1. The open-circuit voltage (V_oc) of the fabricated devices was found to be higher than that of devices based on C₆₀ because the LUMO energy level of the new fullerene derivative was higher than that of C₆₀. Further, the power conversion efficiency (PCE) of these devices was observed to be high when annealing was carried out at 150 °C for 5 min and the thickness of the active layer was 80 nm. The maximum V_oc, short-circuit current density, and PCE of the best device were 0.608 V, 4.393 mA/cm², and 1.29%, respectively.     

Influence of doped PEDOT:PSS on the performance of polymer solar cells

The influence of anode buffer layers of doped poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) on the performance of solar cells made from blends of poly(3-hexylthiophene) and [6,6]-phenyl-C₆₁-buytyric acid methyl ester has been investigated. Different concentration of ethylene glycol were added into the PEDOT:PSS solution to increase its conductivity. The surface roughness of the doped PEDOT:PSS film was changed, which was examined by atomic force microscopy. The best doped device with a power conversion efficiency of 4.39% as compared to 3.41% for the pristine device has been achieved. The enhanced PEDOT:PSS conductivity improved the short circuit current and fill factor of the doped device. The almost constant open circuit voltage indicated the well-established ohmic contact between the anode and active layer irrespective of the doping of the PEDOT:PSS. The changed surface roughness of the doped PEDOT:PSS film did not correlate with the morphology of the consequent active layer and the resultant device performance.     

Characterization of high-photovoltage CuPc-based solar cell structures

Organic solar cells of the configuration ITO/PEDOT:PSS/CuPc/PTCBI/Al (Indium Tin Oxide/poly(3,4-ethylenedioxythiophene): polystyrene sulfonic acid/Copper phthalocyanine/3,4,9,10-perylenetetracarboxylic bisbenzimidazole/Aluminum ) were investigated. A high open circuit voltage (V_OC) of 1.15 V was obtained when the PTCBI layer was 7 nm thick. Lower V_oc values were observed for the same structure with silver, copper and gold electrodes instead of aluminum. However, short-circuit current density (J_SC) with these electrodes was much higher (4 mA/cm²) than in the case of aluminum (0.12 mA/cm²). Incorporating a 10 nm thick CdS interlayer between PTCBI and aluminum resulted in an increase in current density to 0.3 mA/cm². Results were interpreted in terms of a modified CuPc/Al Schottky diode for the thin PTCBI case and a CuPc/PTCBI heterojunction for the thick PTCBI case. Also, the formation of a thin, protective aluminum oxide layer under the aluminum electrode was postulated. For devices with silver, copper and gold electrodes, absence of this protective layer was thought to be the cause of a relatively lower V_oc and higher J_SC.     

Numerical study of electrical behavior of P3HT/PCBM bulk heterojunction solar cell

In this work the program AMPS-1D was used to optimize the performance of the organic solar cells. The cells considered consist of poly(3-HexylThiophène) [P3HT] as electron donors, and (6,6)-phenyl- C61-butyric acid methyl ester [PCBM] as electron acceptor, (P3HT/PCBM) is used as photo-active material, sandwiched between a transparent indium tin oxide (ITO) and layer of poly(3,4 ethylenedioxythiophene)/ poly(styrenesulfonate) (PEDOT/PSS) on top of the ITO electrode and an AL backside contact. The results showed that the optimum thickness of the solar cell is about 400 nm, V_oc = 0.61 at T = 300 K. This is in the good agreement with the corresponding computer simulation value of 0.63 V. The maximum limit for the organic solar cell efficiency is about 8%, provided that the band-gap of the cell is about 1.5 eV.     

Enhancing the durability of polymer solar cells using gold nano-dots

The durability of organic photovoltaic devices is improved by (a) replacing thermally labile poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) with gold nano-dots and (b) stabilizing the morphology of photoactive layers through thermally induced reaction. Gold nano-dots (Au-ND) (3–6 nm in diameter and 0.8 nm in height) were thermally deposited on ITO substrates prior to depositing a hole transporting layer (40 nm) of an azide-functionalized poly(3-hexylthiophene), P1, which was insolubilized by heating to 150 °C. A blend of P1 and [6,6]-phenyl C₆₁-butyric acid methyl ester (PCBM) was deposited and heated to 150 °C prior to the deposition of a Ca/Al cathode. The reaction of P1 with PCBM stabilized the bulk heterojunction film as evidenced by the suppression of crystallization of PCBM. Replacement of PEDOT:PSS with Au-ND, in combination with morphological stabilization, greatly improves the durability of PV devices under accelerated lifetime testing at 150 °C. Power conversion efficiencies (PCE) for the P1:PCBM devices stabilized at 1.25% after 28 h of accelerated testing at 150 °C, whereas conventional P3HT:PCBM devices on PEDOT/ITO dropped to 0.58% after only 7 h of accelerated testing. Prospects for similarly enhancing the durability of highly efficient PV devices are discussed.     

The influence of electrode buffer layers on the performance of polymer photovoltaic devices

The influence of electrode buffer layers (EBLs) on the performance of polymer photovoltaic (PV) devices based on blends of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C₆₁-buytyric acid methyl ester (PCBM) has been investigated. Copper phthalocyanine (CuPc), bathocuproine (BCP) and pentacene are used as EBLs of solar cells to improve the photovoltaic performances, including short circuit current density (Jsc), open circuit voltage (Voc), power conversion efficiency (PCE) and fill factor (FF). The obtained results suggest that the insertion of EBLs can greatly improve the Jsc and PCE of the PV devices. And the effect of thickness of the four EBLs has also been explored and compared. The PV device with 1 nm BCP cathode buffer layer gets the highest PCE, which is 2.6 times that of the PV device without EBL.     

Synthesis and characterization of 2,1,3-benzothiadiazole-thieno[3,2-b]thiophene-based charge transferred-type polymers for photovoltaic application

New low-band-gap copolymers, including thieno[3,2-b]thiophene and 2,1,3-benzothiadiazole, were synthesized as photovoltaic materials. Thiophene was introduced to provide extended π-conjugation length and charge transfer properties. A band gap (E_g^op=1.62 eV, E_g^ec=1.51 eV) of this polymer was investigated through UV-vis spectroscopy and cyclic voltammetry. A bulk heterojunction structure of glass/indium tin oxide (ITO)/PEDOT:PSS/polymer-PCBM(1:3)/LiF/Al was fabricated for investigating photovoltaic properties. PC₇₁BM was used as an acceptor material, due to its increased absorption in the visible region, in comparison with PC₆₁BM. In this polymer, incident photon-to-current conversion efficiency (IPCE) was as high as 50%. Moreover, maximum power conversion efficiency (PCE) of up to 1.72% was achieved under AM 1.5 G conditions. It demonstrated relatively high V_OC (0.67 V) and J_SC (6.86 mA/cm²), while a low fill factor value (0.37) was obtained.     

Effect of CdSe/P3HT composition on electrical and structural properties of bulk hetero-junction solar cell active layer

The use of inorganic nano-semiconductor/polymer blend as the active layer for organic bulk hetero-junction solar cell is an alternative to change and improve the device characteristics and performance. Effects of CdSe/P₃HT composition in the blend and its loading amount in the solvent on the electrical and structural properties of active layers formed were investigated. The results of atomic force microscopy study indicated that the surface roughness of composite active layer could be controlled below 10 nm for the entire range of composite loading amount investigated in this study. The transmission line method experiments have demonstrated that the electrical percolation pathways could be developed at the critical loading amount of CdSe/P₃HT composite, resulting in the abrupt decrease of sheet resistance and significant increase in the power conversion efficiency of ITO/PEDOT:PSS/(CdSe/P₃HT)/Al solar cell.