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The performance of both organic light-emitting diodes (OLEDs) and organic solar cells (OSC) depends on efficient coupling between optical far field modes and the emitting/absorbing region of the device. Current approaches towards OLEDs with efficient light-extraction often are limited to single-color emission or require expensive, non-standard substrates or top-down structuring, which reduces compatibility with large-area light sources. Here, we report on integrating solution-processed nano-particle based light-scattering films close to the active region of organic semiconductor devices. In OLEDs, these films efficiently extract light that would otherwise remain trapped in the device. Without additional external outcoupling structures, translucent white OLEDs containing these scattering films achieve luminous efficacies of 46 lm W-1 and external quantum efficiencies of 33% (both at 1000 cd m-2). These are by far the highest numbers ever reported for translucent white OLEDs and the best values in the open literature for any white device on a conventional substrate. By applying additional light-extraction structures, 62 lm W-1 and 46% EQE are reached. Besides universally enhancing light-extraction in various OLED configurations, including flexible, translucent, single-color, and white OLEDs, the nano-particle scattering film boosts the short-circuit current density in translucent organic solar cells by up to 70%. [ABSTRACT FROM AUTHOR]

Micro-structured organic photovoltaic (OPV) devices on polyethylene terephthalate substrates are produced using direct laser interference patterning (DLIP). The performance of organic solar cells on these substrates is improved by a factor of 1.16, and a power conversion efficiency of 7.70% is achieved. We show that a shorter spatial period of the pattern allows for a stronger light trapping effect in solar cell, as it leads to a longer light path. Moreover, since the patterned structures are located on the outside of the fully encapsulated OPV devices, there are no problems with the roughness induced shunts. [ABSTRACT FROM AUTHOR]

The degradation of sexithiophene cascade organic solar cells is studied. Glass–glass encapsulated devices on indium tin oxide as transparent electrode show efficiencies of 6.6% and degrade within 500 h in illuminated 38 °C/50% RH climate. Fully flexible devices with silver nanowire electrode and alumina barrier achieve 5% efficiency and degrade within 30 h due to electrode failure. [ABSTRACT FROM AUTHOR]

Pulsed laser deposited gallium doped zinc oxide (ZnO:Ga) is reported as transparent top electrode for organic solar cells. In contrast to standard coating techniques, prone to harm organic sublayers and leading to strongly reduced device efficiencies, eclipse pulsed laser deposition (PLD) in argon atmosphere is identified as compatible, nonharmful deposition method for ZnO:Ga, even on top of sensitive organic material. Although PLD is not yet ready for mass production, the experiments reveal and solve crucial process limitations, e.g., droplet impacts, which might be useful also for high yield deposition methods. Optimized ZnO:Ga top electrodes achieve a high mean transparency in the visible spectral range of Tvis = 82.7% and a reasonable sheet resistance of RS = 83 Ω sq−1. The organic photovoltaic devices prepared with this electrode obtained an efficiency of η = 2.9%, almost equal to the efficiency of reference samples using a state-of-the-art metal top contact ( η = 3.0%). The investigations here demonstrate the successful deposition of transparent conductive oxides as top electrode for organic devices and open a new path towards the combination of metal oxides and organic semiconductors. [ABSTRACT FROM AUTHOR]

The article offers information on the use of hybrid electrodes with a combination of ultratransparent poly(3,4-ethylenedioxythiophene) : poly(styrenesulfonate) (PEDOT:PSS) and an evaporated semitransparent silver (Ag) grid for small-molecule organic solar cells. Topics discussed include electrical and optical properties as well as excellent mechanical flexibility of indium-tin oxide (ITO), performance of Organic photovoltaic (OPV) cells and characteristics of various electrodes.

Highly transparent electrodes are demonstrated based on thermally evaporated calcium:silver blend thin-films, which show unusually high transmission well above the expectations from bulk material properties and thin film optics. These electrodes exhibit a low sheet resistance of 27.3 Ω/, combined with an extraordinarily high mean transmittance of 93.0% in the visible spectral range (σdc/σopt = 186.7), superior to the commonly used inorganic electrodes made from indium tin oxide (ITO). Additionally, the metal blend electrode is flexible, showing a constant sheet resistance down to a bending radius of 10 mm and can be employed on top of organic devices without causing damage to the organic material. The spontaneously formed unique microstructure of a polycrystalline Ag network with randomly distributed nanoapertures, surrounded by a calcium shell, enables broadband transmittance enhancement due to amplified plasmonic coupling. Consequently, top-illuminated organic solar cells using such metal blend electrodes achieve a power conversion efficiency of 7.2% (which defines a new record for top illuminated organic solar cells) and even exceed the efficiency of similar bottom-illuminated reference solar cells (6.9%) employing common ITO electrodes. [ABSTRACT FROM AUTHOR]

The great potential of solution-processed metal nanowire networks utilized as a transparent electrode has attracted much attention in the last years. Typically, silver nanowires are applied, although their replacement by more abundant and cheaper materials is of interest. Here, a hydrazine-free synthesis route for high aspect ratio copper nanowires is used to prepare conductive networks showing an enhanced electrode performance. The network deposition is done with a scalable spray-coating process on glass and on polymer foils. By a pressing or an annealing step, highly conductive transparent electrodes are obtained, and they reveal transmittance-resistance values similar to indium tin oxide (ITO) and networks made of silver nanowires. The application potential of the copper nanowire electrodes is demonstrated by integrating them into an evaporated small-molecule organic solar cell with 3% efficiency. [ABSTRACT FROM AUTHOR]

Abstract: Percolation networks from silver nanowires can be used as a transparent electrode and promising alternative to the commonly used ITO. Here, the deposition of such a nanowire based network by dip coating, a versatile and scalable method, is described and characterized in detail. After identifying appropriate processing parameters, nanowire grids with conductivity and transmittance values rivaling ITO have been achieved. As a main issue, the roughness of the film was addressed and the influence on the device in terms of shunt paths was investigated. Using this network as anode, small molecule organic solar cells with varying stack structure were fabricated and yield efficiencies comparable to cells on ITO. [Copyright &y& Elsevier]

Abstract: We have developed semi-transparent n–i–p organic solar cells (OSC) with free-standing multi-wall carbon nanotube (f-CNT) sheets as transparent top electrodes. By a simple and damage-free room temperature orthogonal liquid solution assisted self-laminating process, f-CNT top electrodes are successfully deposited on top of ZnPc:C60 bulk heterojunction small molecule OSCs. The cells show high fill factors above 58% as well as efficiencies up to 1.5% and greater long-term stability compared to the device having a metal electrode. For the given cell structure with f-CNT semi-transparent electrodes, the influence of an optical spacer on light absorption is studied by a systematic variation of the hole transport layer thickness, supported by optical simulations. The results strongly indicate that OSCs with f-CNT top electrodes and optimized thin film stack are highly promising for semi-transparent OSCs, which can be used in tandem devices, in tinted smart windows, and similar applications by a simple and damage-free process in roll-to-roll configuration that can be scaled to large area manufacturing. [Copyright &y& Elsevier]

We report on efficient and stable ITO-free small molecule organic solar cells with conductive poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) electrodes using a post-treatment process, causing selective removal of PSS. The solar cells with post-treated PEDOT:PSS electrodes show significantly improved short circuit current densities and efficiencies compared to untreated devices. Moreover, the removal of PSS by the post-treatment significantly improves the lifetime of devices, which are more resistant to loss of fill factor compared to untreated devices. [ABSTRACT FROM AUTHOR]

Flexible aluminum moisture barrier films are shown to meet ultra-barrier requirements with water vapor transmission rates as low as 1*10 −4 g/m 2 /day at 38 °C and 90% R.H. These low transmission rates are achieved by lamination of two films that are independently processed on individual substrates. The integration in organic electronic devices like organic solar cells or OLEDs is particularly easy in a single lamination step, since an existing aluminum electrode can be utilized as one half of the moisture barrier. The resulting laminate maintains flexibility of the device and improves the barrier quality by an order of magnitude compared to conventional stacking of two barriers. Organic solar cells with this type of encapsulation are manufactured and aged in controlled climate. They do not exhibit significant extrinsic degradation. [ABSTRACT FROM AUTHOR]

Planarization and filling voids between wires are key issues when using nanowire electrodes in flexible solar cells such as organic photovoltaics (OPV). For this purpose, we use poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT: PSS) which leads to an electrically well connected silver nanowire (AgNW) network. Furthermore, the use of water based PEDOT: PSS leads to humidity assisted AgNW fusing, resulting in a maximum processing temperature of only 120 °C. OPV cells using this AgNW/PEDOT: PSS transparent electrodes exhibit power conversion efficiencies up to 7.15%. Moreover, OPV devices on PET substrates with an alumina encapsulation and barrier adhesive show excellent mechanical flexibility. [ABSTRACT FROM AUTHOR]

Recently, organic solar cells have demonstrated high power conversion efficiencies, but extrinsic device stability remains to be a challenge. Often, delamination of the cathode upon water ingress leads to a massive active area loss and to a strong decrease in efficiency. We present highly efficient organic solar cells with an oligothiophene-based donor and two different cathodes. Devices are aged at four different climates under continuous illumination. Al and MoO 3 /Cr/Al cathodes are compared. Additional interlayers are introduced for enhanced cathode adhesion. Aging in different climates reveals a strong dependency of the degradation speed on absolute humidity for standard Al cathodes. However, using additional interlayers, degradation seems to be almost decoupled from the applied climate and device degradation is slowed immensely. Parallel WVTR measurements of the AlO x barrier allow for the assessment of absolute water quantities until devices are degraded to half of their initial efficiency: 24 g m 2 are found for standard Al cathodes, while devices with additional interlayers reach 58 g m 2 . This difference is related to a completely different aging behavior, which trades strong short-circuit current density losses for moderate fill-factor losses. [ABSTRACT FROM AUTHOR]

Abstract: We report on transparent stand alone C60 top electrodes for small molecule based organic photovoltaic cells. All device layers (including bottom and top electrode) are thermally evaporated in vacuum, guaranteeing fast, reliable, high-purity and low-cost processing. Employing an organic compound as electrode avoids refractive index mismatch between contact and photo-active layer which results in an increased number of photons reaching the absorber layers. The conductivity of C60 is improved from 10−8 S/cm to remarkable 4.97S/cm by optimized molecular n-type doping. Furthermore, it is shown that high doping concentrations change the absorption behavior of C60, leading to transmittance values over 70% for wavelengths larger than 600nm with a weak dependence on layer thickness. Organic solar cells employing such an optimized n-doped C60 top electrode (thickness 200nm, doping concentration 16wt%) exhibit power conversion efficiencies of 1.53%. Electrical device simulations based on a discretized equivalent circuit model reveal an efficient lateral charge transport in n-doped C60 electrodes over a few 100µm. In combination with a supporting grid electrode (usually employed for large area photovoltaic applications), n-doped C60 might replace ITO and fill the lack of transparent conductive top electrodes required for roll-to-roll processed semi-transparent organic devices or devices on opaque substrates. [Copyright &y& Elsevier]

Abstract: The performance of organic solar cells strongly depends on the nanoscale structure of the used mixed absorber layer. Utilizing photoconductive and conductive atomic force microscopy (pcAFM and cAFM), as well as transmission X-ray microscopy (TXM), we investigate the influence of different substrate temperatures T sub on the thin-film structure and local photocurrent in bulk-heterojunctions (BHJs) of vacuum deposited zinc phthalocyanine (ZnPc) and Buckminsterfullerene (C60) mixed absorber layers. In this paper, we present topography maps, photocurrent maps under short-circuit current conditions, dark-current maps, and TXM images with high lateral resolution down to 25nm. We observe a strong influence of the substrate temperatures during deposition T sub on the nanoscopical segregation of the two components in the BHJ. This segregation leads to a spatial extension of the dark-current and a reduced short-circuit current at higher substrate deposition temperatures T sub. [Copyright &y& Elsevier]

Abstract: We investigate various electrode combinations of bottom and top contacts for organic photovoltaic (OPV) cells. Silver (Ag), indium tin oxide (ITO), poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), and silver nanowires (AgNW) are used as bottom electrodes. As top electrodes, thin silver layers (t-Ag) and free-standing carbon nanotube (f-CNT) sheets are employed. The manufactured zinc phthalocyanine (ZnPc): fullerene C60 small molecule bulk heterojunction OPV cells with different kinds of bottom electrodes show efficiencies of 1.9∼2.2% and 1.1∼1.5%, when comprised of t-Ag and f-CNT top contacts, respectively. We demonstrate alternative electrodes beyond ITO, silver, and aluminum, which can be readily used for organic photovoltaics technology. [Copyright &y& Elsevier]

Abstract: In this work, we use different encapsulations to protect vacuum-evaporated small molecule organic solar cells with a simple p-i-i-stack for lifetime studies. Our devices use ZnPc and C60 as active materials. Lifetimes (T50) in a range from 300h for un-encapsulated devices to 4000h for glass-encapsulated have been observed. We use a model to distinguish between the water vapor transmission rate (WVTR) of the barrier and an additional WVTR of the aluminum top electrode. For all observed devices a loss of 50% of initial efficiency is observed when 10mgm−2 water entered the device. The losses are related to a reduction of short circuit current density only, whereas open circuit voltage and fill factor remains unaffected. We relate this to an interaction of the water molecules with C60. [Copyright &y& Elsevier]