A comparative assessment of surface microstructure and electrical conductivity dependence on co-solvent addition in spin coated and inkjet printed poly(3,4-ethylenedioxythiophene):polystyrene sulphonate (PEDOT:PSS)

This study focuses on the fabrication of poly(3,4-ethylenedioxythiophene):polystyrene sulphonate (PEDOT:PSS) thin films by inkjet printing and investigates the developed surface morphology and electrical conductivity of the printed films as a function of the concentration of dimethyl sulfoxide (DMSO), added as conduction enhancing co-solvent, and Surfynol, added as a surfactant. The printed films are compared with PEDOT:PSS films fabricated by the traditional spin coating technique. Measurements of the surface tension justify including surfactant as a processing additive, where addition of 1% Surfynol results in substantial decrease of the surface tension of the PEDOT:PSS solution, whilst it also increases film surface roughness by an order of magnitude for both fabrication methods. The addition of 5 wt% DMSO is shown to result in a 10³ decrease in sheet resistance for both spin coated and inkjet printed films with both processing routes demonstrating decrease in surface roughness and coarsening of PEDOT grains as a function of the co-solvent concentration, whilst X-ray photon spectroscopy showed an increase in the surface PEDOT to PSS ratio from 0.4 to 0.5. Inkjet printed films have lower sheet resistance than the corresponding spin coated films, whilst atomic force microscopy reveals a coarser surface morphology for the inkjet printed films. The findings in this work point out at the decrease of sheet resistance due to coarsening of PEDOT grains which is linked to a decrease of surface roughness for small RMS values associated with the PEDOT grains. However, the higher surface roughness generated when Surfynol surfactant was added was not detrimental to the film’s in-plane conductivity due to the fact that these higher roughness values were unrelated to the PEDOT grains.     

In-plane conduction characterisation and charge transport model of DMSO co-doped,inkjet printed Poly(3,4-ethylenedioxythiophene): Polystyrene sulfonate (PEDOT:PSS)

The technologically important inkjet printed poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) films, at different extents of co-doping with dimethyl sulfoxide DMSO, have been studied in terms of in-plane charge transport and electric field force microscopy (EFM). Similarly to past studies of spin coated PEDOT:PSS films, room temperature conductivity is enhanced by a factor of 10³ to 130 S cm⁻¹ on the addition of 5% DMSO, Hall probe analysis demonstrated a decrease in contact resistance from 10⁶ Ω to 10⁴ Ω whilst variable-temperature conductivity analysis shows an increase in the VRH exponent from 0.25 to 0.5 signifying a charge transport evolution from Mott Variable Range Hopping in 3-dimensions to a pseudo 1-dimensional Variable Range Hopping. In addition, electric field force microscopy (EFM) showed a corresponding threefold increase in PEDOT grain size. Further analysis was conducted to determine the hopping length and the ratio of the hopping length versus localization length in the electron transport model.     

Indium zinc oxide ohmic contact to poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) induced by UV light

In this research, we investigated the I–V characteristics of ITO/PEDOT:PSS/InZnO devices for two sets of samples. The first set is composed of PEDOT:PSS as-prepared, while the second set is composed of PEDOT:PSS irradiated by UV light source. We found that UV irradiation improves the electrical conductivity of the fabricated devices and yields to ohmic contact. Based on the UPS measurements, it was found that UV irradiation leads to an increase in the work function and the enhancement of electrical conductivity of PEDOT:PSS films. XPS and AFM measurements indicate that conformational changes of the PEDOT:PSS films are responsible for this behavior. We also studied the effect of storage on the electrical properties of our devices. No significant changes of electrical characteristics have been found after storing the devices for a period of 30 days.     

Conductivity,work function,and environmental stability of PEDOT:PSS thin films treated with sorbitol

The electrical properties of poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) thin films deposited from aqueous dispersion using different concentrations of sorbitol have been studied in detail. Although it is well known that sorbitol enhances the conductivity of PEDOT:PSS thin films by three orders of magnitude, the origin and consequences of sorbitol treatment are only partly understood and subject of further study. By thermal annealing of spin coated PEDOT:PSS/sorbitol films and simultaneously monitoring the conductivity, we demonstrate that the strong increase in conductivity coincides with evaporation of sorbitol from the film. Hence, sorbitol is a processing additive rather than a (secondary) dopant. Scanning Kelvin probe microscopy reveals that sorbitol treatment causes a reduction of the work function from 5.1 eV to 4.8–4.9 eV. Sorbitol also influences the environmental stability of the films. While the conductivity of the pristine PEDOT:PSS films increases by about one order of magnitude at ∼50% RH due to an ionic contribution to the overall conductivity, films prepared using sorbitol exhibit an increased environmental stability with an almost constant conductivity up to 45% RH and a slight decrease at 50% RH. The higher stability results from a reduced tendency to take up water from the air, which is attributed to a denser packing of the PEDOT:PSS after sorbitol treatment.     

Highly Customizable All Solution–Processed Polymer Light Emitting Diodes with Inkjet Printed Ag and Transfer Printed Conductive Polymer Electrodes

Inkjet and transfer printing processes are combined to easily form patterned poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) films as top anodes of all solution–processed inverted polymer light emitting diodes (PLEDs) on rigid glass and flexible plastic substrates. An adhesive PEDOT:PSS ink is formulated and fully customizable patterns are obtained using the inkjet printing process. In order to transfer the patterned PEDOT:PSS films, adhesion properties at interfaces during multistep transfer printing processes are carefully adjusted. The transferred PEDOT:PSS film on the plastic substrates shows not only a sheet resistance of 260.6 Ω/□ and a transmittance of 92.1% at 550 nm wavelength but also excellent mechanical flexibility. The PLEDs with spin‐coated functional layers sandwiched between the transferred PEDOT:PSS top anodes and inkjet‐printed Ag bottom cathodes are fabricated. The fabricated PLEDs on the plastic substrates show a high current efficiency of 10.4 cd A^?1 and high mechanical stability. It is noted that because both Ag and PEDOT:PSS electrodes can be patterned with a high degree of freedom via the inkjet printing process, highly customizable PLEDs with various pattern sizes and shapes are demonstrated on the glass and plastic substrates. Finally, with all solution process, a 5 × 7 passive matrix PLED array is demonstrated.     

Optical properties and conductivity of PEDOT:PSS films treated by polyethylenimine solution for organic solar cells

We report on conductivity and optical property of three different types of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) films [pristine PH1000 film (PH1000-p), with 5 wt.% ethylene glycol additive (PH1000-EG) and with sulfuric acid post-treatment (PH1000-SA)] before and after polyethylenimine (PEI) treatment. The PEI is found to decrease the conductivity of all the PEDOT:PSS films. The processing solvent of 2-methoxyethanol is found to significantly enhance the conductivity of PH1000-p from 1.1 up to 744 S/cm while the processing solvent of isopropanol or water does not change the conductivity of PH1000-p much. As for the optical properties, the PEI treatment slightly changes the transmittance and reflectance of PH1000-p and PH1000-EG films, while the PEI leads to an substantial increase of the absorptance in the spectral region of 400–1100 nm of the PH1000-SA films. Though the optical property and conductivity of the three different types of PEDOT:PSS films vary with the PEI treatment, the treated PEDOT:PSS films exhibit similar low work function. We demonstrate solar cells with a simple device structure of glass/low-WF PEDOT:PSS/P3HT:ICBA/high-WF PEDOT:PSS cells that exhibit good performance with open-circuit voltage of 0.82 V and fill factor up to 0.62 under 100 mW/cm² white light illumination.     

Effects of tetramethylene sulfone solvent additives on conductivity of PEDOT:PSS film and performance of polymer photovoltaic cells

A solvent additive in PEDOT:PSS solution is one of many methods to improve the conductivity of the poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films. We explore a new type of the solvent additive, namely tetramethylene sulfone (TMS), for the fabrication of the PEDOT:PSS conductive layer in the ITO/PEDOT:PSS/P3HT:PCBM/TiO_x/Al polymer photovoltaic cells, in comparison to a more common dimethyl sulfoxide (DMSO) solvent additive. At optimal conditions, the TMS additive at 10 wt.% has been found to enhance the conductivity of pristine PEDOT:PSS films from 0.04 S/cm up to approximately 189 S/cm, compared with the highest conductivity for the case of the DMSO additive at 15 wt.% of 117 S/cm. Possible mechanisms of this conductivity enhancement, relating to the polymer conformation and the film morphology, have been investigated by Raman spectroscopy, X-ray diffraction, atomic force microscopy, and transmission electron microscopy. The performance of the polymer photovoltaic cells fabricated with the solvent additives PEDOT:PSS films follows a similar trend to the conductivity of the films as a function of the additive concentration. The additives mainly lead to greater short circuit current density (J_sc) of the photovoltaic cells. The highest power conversion efficiency (PCE) of 2.24% of the device has been obtained with the 10 wt.% TMS additive of, compared to the PCE of 1.48% for the standard device without solvent additive.     

Electrical characterization of inorganic-on-organic diode based InP and poly(3,4-ethylenedioxithiophene)/poly(styrenesulfonate) (PEDOT:PSS)

The electronic properties of metal–organic semiconductor-inorganic semiconductor diode between InP and poly(3,4-ethylenedioxithiophene)/poly(styrenesulfonate) (PEDOT:PSS) polymeric organic semiconductor film have been investigated via current–voltage and capacitance–voltage methods. The Al/PEDOT:PSS/p-InP contact exhibits a rectification behavior with the barrier height value of 0.98 eV and with the ideality factor value of 2.6 obtained from their forward bias current voltage (I–V) characteristics at the room temperature greater than the conventional Al/p-InP (0.83 eV, n = 1.13). This increase in barrier height and ideality factor can be attributed to PEDOT:PSS film formed at Al/p-InP interface.     

Highly branched green phosphorescent tris-cyclometalated iridium(III) complexes for solution-processed organic light-emitting diodes

A series benzoimidazole-based dendritric complexes of iridium dendrimers containing Fréchet-type dendrons with peripheral fluorenyl surface groups have been synthesized. These iridium dendrimers are green-emitting with high phosphorescence quantum yield, and can be spin-coated as films of good quality. From cyclic voltammograms (CV), high onset potentials at 1.42–1.58 V due to the peripheral fluorene group were observed. Device from a second generation dendrimer 17 with structure of ITO/PEDOT:PSS/CBP: 20 wt% 17/TPBI/LiF/Al (PEDOT:PSS = poly(ethylene dioxythiophene): polystyrenesulfonate and CBP = bis(N-carbazolyl)biphenyl) has the best performance: maximum external quantum efficiency of 13.58% and maximum current efficiency of 45.7 cd/A. Space-charge-limited current (SCLC) flow technique was used to measure the mobility of charge carriers in the blend films of the compounds in CBP. Blend films of higher generation dendrimers have lower hole mobility, albeit with higher device efficiencies.     

Improvement of electrical conductivity of PEDOT:PSS films by 2-Methylimidazole post treatment

The electrical conductivity of poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) films was significantly improved without losing the optical transparency by treating the films with solution of 2-Methylimidazole in ethanol. The maximum electrical conductivity of such a thin film reached 930 S cm⁻¹, more than 1150 order of magnitude higher than that of pure PEDOT:PSS film. The mechanism of conductivity enhancement of treated thin PEDOT:PSS films was explored by atomic force microscopy (AFM) and UV/VIS spectrophotometer. The AFM scans show that the surface of the 2-Methylimidazole treated PEDOT:PSS layer is smoother than that of the pristine PEDOT:PSS thin film. Improvement in the morphology, electrical and optical properties of PEDOT:PSS films makes them highly suitable for numerous applications in optoelectronic devices.     

Composite film of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) and MoO3 as an efficient hole injection layer for polymer light-emitting diodes

We demonstrate improved performances in polymer light-emitting diodes (PLEDs) using a composite film of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and MoO₃ powder as a hole injection layer. The PLED with the composite film exhibits the current efficiency of 13.5 cd/A, driving voltage of 3.4 V, and half lifetime of 108.1 h, while those values of the PLED with a pristine PEDOT:PSS was 11.3 cd/A, 3.8 V, and 41.5 h, respectively. We also analyze the morphological, optical and electrical properties of the composite films by atomic force microscopy (AFM), UV–Vis-IR absorption, and ultraviolet photoemission spectroscopy (UPS). This work suggests that mixing MoO₃ into PEDOT:PSS is a simple and promising technique for use solution-based devices as an hole injection layer.     

Handheld and automated ultrasonic spray deposition of conductive PEDOT:PSS films and their application in AC EL devices

In this contribution we explore the spray deposition technique to achieve smooth films based on the conductive polymer PEDOT:PSS. Two different spray systems were used and compared namely: (a) handheld airbrush and (b) automated ultrasonic spray system. For each system a number of parameters were pre-adjusted during coating control experiments such as spray head distance, angle and cone for airbrush as well as flow rate, power and focus for ultrasonic nozzle. Water-based solutions of PEDOT:PSS having 20% of N-methylpyrrolidone (NMP) were sprayed on glass substrates at temperatures ranging from 75 to 150 °C. The resulting films were further chemically treated with ethylene glycol (EG) and evaluated with respect to their morphological, electrical and optical properties. Before EG-treatment the ultrasonic spraying resulted in smoother films with conductivity up to 2–3.9 times higher than their airbrushed counterparts. Deposition temperature proved to have minor effect on the morphological and electro-optical properties of PEDOT:PSS films. On the other hand, the film conductivity was enhanced, peaking at 610.1 S cm⁻¹ for ultrasonic spraying, when further chemically modified by EG. IR microspectroscopy mapping analysis, Raman spectroscopy and XRD data indicated a phase-separation between PEDOT and PSS chains and increasing crystallinity in the ultrasonically sprayed films. The application of such PEDOT:PSS films as transparent electrode in flexible AC EL devices is demonstrated.     

Preparation of lateral spin-valve structure using doped conducting polymer poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate)

To perform four-terminal nonlocal spin-valve measurements on organic spin-valves, we fabricated lateral spin-valve devices consisting of doped conducting polymer poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) [PEDOT:PSS] and ferromagnetic Ni₈₀Fe₂₀ narrow line (width: 530 nm) electrodes. Although the formula of the nonlocal magnetoresistance with the parameters of doped conducting polymers predicts sufficient nonlocal magnetoresistance, we could not observe any spin signal. The spin diffusion length in the doped PEDOT:PSS device does not appear to be as long as those predicted by both the Elliott–Yafet mechanism and the theory of spin relaxation in organic disordered solids.     

Pt–free counter electrodes based on modified screen–printed PEDOT:PSS catalytic layers for dye–sensitized solar cells

One of the most highlighted advantages of dye-sensitized solar cells (DSSCs) consists in the possibility to apply simple and low-cost printing techniques and solution processable materials for their assembling. Here, we report on screen-printed Pt–free counter electrodes (CEs) based on poly(3,4–ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) dispersions with different content of rheological agent – hydroxyethyl cellulose (HEC). These PEDOT:PSS dispersions, having measured pseudoplastic and thixotropic rheological behaviour, were screen–printed onto FTO glasses. The content of rheological agent in PEDOT:PSS catalytic layers showed an effect on measured thickness, electrochemical properties, specific conductivity and subsequently on the evaluated photovoltaic performance of DSSCs. The PEDOT:PSS CE with the 0.03 wt% of HEC achieved the best electrochemical performance and specific conductivity (80 S cm⁻¹), the lowest thickness of 200 nm and transparency in VIS light spectrum over 60%. DSSCs based on this PEDOT:PSS CE reached the highest conversion efficiency of 4.2% which is only approximately 40% lower value than η=6.9% evaluated for Pt CE.     

Transparent and flexible amorphous InZnAlO films grown by roll-to-roll sputtering for acidic buffer-free flexible organic solar cells

We report on transparent and flexible amorphous In–Zn–Al–O (a-IZAO) films prepared by roll-to-roll (RTR) sputtering for use as anodes in acidic buffer free flexible organic solar cells (FOSCs). The presence of Zn and Al structural stabilizers in the In₂O₃ matrix produced a completely amorphous structure with the high optical transmittance of 89.25% and the low resistivity of 2.123 × 10⁻³ Ω-cm, as well as the high work function of 5.14 eV, making the a-IZAO films suitable for use as flexible anodes for FOSCs. In addition, the a-IZAO films showed no change in resistance (ΔR) during outer and inner bending fatigue tests due to their good mechanical flexibility. Relative to the power conversion efficiency (1.944%) of a PEDOT:PSS-based FOSCs, a FOSC fabricated by using an a-IZAO anode and without the use of acidic PEDOT:PSS buffer showed greater power conversion efficiency (2.509%), owing to the absence of interfacial reactions between the acidic PEDOT:PSS and the a-IZAO anode.     

Thermal degradation mechanisms of PEDOT:PSS

The thermal stability of thin (50 nm) PEDOT:PSS films, was investigated by dc conductivity measurements, X-ray and UV photoelectron spectroscopies as a function of heating temperature and heating time. The mechanism of electrical conductivity as a function of temperature is consistent with a hopping type carrier transport. The electrical conductivity decreased, as a function of time, in agreement with a granular metal type structure, in which aging is due to the shrinking of the PEDOT conductive grains. XPS and UPS spectra indicate that conformational changes of the PEDOT:PSS film are responsible for this behaviour and a model for these modifications is proposed.     

MoO3/Au/MoO3–PEDOT:PSS multilayer electrodes for ITO-free organic solar cells

The effect of the MoO₃–PEDOT:PSS composite layer in the MoO₃/Au/MoO₃–PEDOT:PSS multilayer electrode on the power conversion efficiency of ITO-free organic solar cells (OSCs) was evaluated. The MoO₃ (30 nm)/Au(12 nm)/MoO₃–PEDOT:PSS (30 nm)/PEDOT:PSS structure showed ~7% more optical transmittance than the MoO₃ (30 nm)/Au (12 nm)/MoO₃(30 nm)/PEDOT:PSS structure at 550 nm wavelength. The OSCs using MoO₃/Au/MoO₃–PEDOT:PSS multilayer electrodes as anodes showed a considerable improvement in power conversion efficiency (PCE), from 1.84% to 2.81%, comparable to ITO based OSCs with PCE of 2.89%. This improvement is attributed to the suppression of MoO₃ dissolution by the acidic hole transport layer (HTL) PEDOT:PSS on the MoO₃/Au/MoO₃–PEDOT:PSS multilayer electrode, resulting in high J_sc, V_oc and FF of the OSCs. This composite based multilayer electrode was shown to be a promising replacement in ITO-free flexible optoelectronic devices.     

An inverted,organic WORM device based on PEDOT:PSS with very low turn-on voltage

An organic Write-Once-Read-Many (WORM) device based on poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) as the active layer was fabricated with an inverted architecture. Insertion of an ultrathin layer of poly(methylmethacrylate) (PMMA) between the bottom electrode and the PEDOT:PSS resulted in a systematic and substantial decrease in turn-on voltage, from 7.0 V to less than 1.0 V. An optimal thickness of the PMMA layer was found to yield the lowest consistent turn-on voltage of ∼0.8 V, with 0.5 V being the lowest value of all fabricated devices. The switching mechanism was attributed to filamentary doping of the PEDOT:PSS. Insertion of the PMMA acted to protect the underlying ZnO from being etched by the acidic PEDOT:PSS as well as to improve its wetting properties. Devices were demonstrated on both ITO and aluminum bottom electrodes, with aluminum yielding the highest ON/OFF ratios in the study. Owing to their inverted architecture, the devices demonstrated good stability, and the retention time of the ON-state was determined to be greater than twenty months while stored in air for devices with ITO bottom electrodes. In addition to deposition via spin-coating, blade-coating was demonstrated as a viable processing technique for applications requiring rapid or large-area manufacturing.     

Metal salt modified PEDOT:PSS as anode buffer layer and its effect on power conversion efficiency of organic solar cells

The effects of metal chlorides such as LiCl, NaCl, CdCl₂ and CuCl₂ on optical transmittance, electrical conductivity as well as morphology of PEDOT:PSS films have been investigated. Transmittance spectra of spun PEDOT:PSS layers were improved by more than 6% to a maximum of 94% in LiCl doped PEDOT:PSS film. The surface of the PEDOT:PSS films has exhibited higher roughness associated with an increase in the electrical conductivity after doping with metal salts. The improvement in the physical properties of PEDOT:PSS as the hole transport layer proved to be key factors towards enhancing the P3HT:PCBM bulk heterojunction (BHJ) solar cells. These improvements include significantly improved power conversion efficiency with values as high as 6.82% associated with high fill factor (61%) and larger short circuit current density (∼18 mA cm⁻²).     

The enhancement of electrical and optical properties of PEDOT:PSS using one-step dynamic etching for flexible application

The conductivity enhancement of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) by dynamic etching process was investigated to introduce the outstanding and simplest method for soft electronics. Four different samples which were pristine PEDOT:PSS, PEDOT:PSS doped with 5 wt.% DMSO, PEDOT:PSS with dipping process, and PEDOT:PSS with dynamic etching process were prepared to compare the properties such as conductivity, morphology, relative atomic percentage, and topography. All samples were characterized by four point probe, current atomic force microscopy (C-AFM), X-ray photoelectron spectroscopy (XPS), and UV–visible spectroscopy. The conductivity of the sample with dynamic etching process showed the highest value as 1299 S/cm among four samples. We proved that the dynamic etching process is superior to remove PSS phase from PEDOT:PSS film, to flow strong current through entire surface of PEDOT:PSS, and to show the smoothest surface (RMS 2.28 nm). XPS analysis was conducted for accurate chemical and structural surface environments of four samples and the relative atomic percentage of PEDOT in the sample with dynamic etching was the highest as 29.5%. The device performance of the sample with the dynamic etching process was outstanding as 10.31 mA/cm² of J_sc, 0.75 eV of V_oc, 0.46 of FF, and 3.53% of PCE. All properties and the device performance for PEDOT:PSS film by dynamic etching process were the most excellent among the samples.