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In recent years there has been an increasing interest to integrate optical sensing in mobile displays, for instance, for biometric fingerprint scanning functionality. There are several routes to incorporate optical fingerprint functionality within the full display area, each with their own benefits and challenges. Here we investigate the different integration routes using large-area, ultra-thin imagers based on organic photodiodes.

To realize the potential of artificial intelligence in medical imaging, improvements in imaging capabilities are required, as well as advances in computing power and algorithms. Hybrid inorganic–organic metal halide perovskites, such as methylammonium lead triiodide (MAPbI3), offer strong X-ray absorption, high carrier mobilities (µ) and long carrier lifetimes (τ), and they are promising materials for use in X-ray imaging. However, their incorporation into pixelated sensing arrays remains challenging. Here we show that X-ray flat-panel detector arrays based on microcrystalline MAPbI3 can be created using a two-step manufacturing process. Our approach is based on the mechanical soft sintering of a freestanding absorber layer and the subsequent integration of this layer on a pixelated backplane. Freestanding microcrystalline MAPbI3 wafers exhibit a sensitivity of 9,300 µC Gyair–1 cm–2 with a μτ product of 4 × 10–4 cm2 V–1, and the resulting X-ray imaging detector, which has 508 pixels per inch, combines a high spatial resolution of 6 line pairs per millimetre with a low detection limit of 0.22 nGyair per frame.

A curved image sensor on plastic foil has been developed for cone beam computed tomography (CBCT) X-ray imaging. The image sensor of about 6 × 8 cm2 size has been built on a thin polyimide foil with an indium gallium zinc oxide (IGZO) backplane and an organic photodetectors (OPD) frontplane. A flexible cesium iodide (CsI) scintillator has been attached to the optical sensor with 480 × 640 pixels of 126 µm size. Dark current density of the OPD was low with less than 10−7 mA/cm2 at −2 V, while an external quantum efficiency (EQE) of about 50% was reached in the visible wavelength range matched to the scintillator output. The image quality of the digital X-ray detector allowed for 3D reconstruction images of a bone phantom on a rotating stage with a lab setup. The curved detector with 32 cm curvature radius opens up the path for very compact CBCT gantries with largely reduced footprint.

We combine a low dark current and high-detectivity near-infrared (NIR)-sensitive organic photodetector with a high-resolution 508 pixels per inch (ppi) oxide thin-film transistor (TFT) backplane to create a large-area thin NIR detector, using processes that are compatible with flat-panel display fabrication. The detector is characterized showing high uniformity and linearity. With the use of a NIR light source, the detector is capable of imaging the (pattern of) veins under the skin in reflection, leading to improved biometric authentication.

We present large-area photodetector arrays in combination with a thin-film optical collimator for under-display fingerprint authentication in next-generation smartphones. The fabrication is compatible with flat panel display processes and based on an oxide TFT backplane with a printed organic photodiode frontplane. The functionality behind an AMOLED display is demonstrated.

Patterning organic materials by photolithography enables not only high-resolution, side-by-side RGB OLED arrays, but also the introduction of organic photodetector in the same frontplane. We show patterned active matrix displays processed on flexible backplane. Furthermore, we demonstrate OPD patterning proof-of-concept. These are the building blocks allowing in-cell optical fingerprint sensor.

In order to protect a flexible OLED on plastic foil against water from the ambient atmosphere a top and bottom thin-film encapsulation (TFE) is necessary. A TFE stack SiN-OCP-SiN with getter in OCP results in excellent shelf lifetime. However, the getter particles result in light scattering that is lost upon water ingress in the stack. As a result spots of reduced electroluminescence are observed during exposure to the ambient atmosphere that limit the practical lifetime of the device drastically. For the bottom emitting OLED we reduced the getter content in the bottom barrier to a level that does not exhibit visible light scattering. The reduced getter capacity with respect to the top barrier does not result in a lower performance of the bottom barrier due to the lower pinhole density in SiN-ITO with respect to Al-SiN. The projected shelf lifetime at ambient conditions is 10 years. © 2018 Elsevier B.V.

Quality Assurance (QA) in hadron therapy is crucial to ensure safe and accurate dose delivery to patients. This can be achieved with fast, reliable and high-resolution detectors. In this paper, we present a novel solution that combines a triple Gas Electron Multiplier (GEM) and a highly pixelated readout based on a matrix of organic photodiodes fabricated on top of an oxide-based thin-film transistor backplane. The first LaGEMPix prototype with an active area of 60 × 80 mm2 was developed and characterized using low energy X-rays. The detector comprises a drift gap of 3.5 mm, a triple-GEM stack for electron amplification, and a readout featuring 480 × 640 pixels at a 126 µm pitch. Here, we describe the measurements and results in terms of spatial resolution for various experimental configurations. A comparison with GAFCHROMIC® films and the GEMPix detector used in the charge readout mode was performed to better understand the contribution to the spatial resolution from both the electron diffusion and the isotropic emission of photons. The measurements were compared to Monte Carlo simulations, using the FLUKA code. The simulation predictions are in good agreement with the GEMPix results. Future plans with respect to applications in hadron therapy are discussed.

Quality Assurance in hadron therapy is crucial to ensure a safe and accurate dose delivery to the patients. This requires fast and reliable detectors with high spatial resolution. A first LaGEMPix prototype that combines a triple Gas Electron Multiplier and a highly pixelated readout based on a matrix of organic photodiodes coated on an oxide thin film transistor backplane has been built. The first version of the LaGEMPix has proven to have a limited spatial resolution, mainly attributed to the isotropic emission of the scintillation photons within the GEM holes. To improve the spatial resolution and confirm our predictions of the role of the photons, we built a new version of the detector with a reduced gap between the last GEM foil and the readout. Experimental results acquired using different methods and experimental set-ups show that the spatial resolution significantly improved with the new design.

Using flat-panel compatible processes we realized 6x8 cm, 200-ppi active-matrix imagers with solution-processed, ultrathin organic photodiodes and demonstrate its performance in a biometric palmprint detector.

We present a thin-film dual-layer bottom barrier on polyimide that is compatible with 350°C backplane processing for organic light-emitting diode displays and that can facilitate foldable active-matrix organic light-emitting diode devices with a bending radius of

Side leakage experiments have been performed on the organic interlayer, so-called organic coating for planarization (OCP), in a hybrid thin-film encapsulation (TFE) stack based on two silicon nitride (SiN) barrier layers that was developed for organic light-emitting diodes (OLED). To measure the side leakage into OCP, a metallic Ca thin-film monitor can be used. However, the water uptake capacity of the Ca monitor affects the measurements. Here, we eliminated the contribution of the Ca layer from the measurement by variation of the Ca thickness and by measuring the side leakage until it reaches the Ca layer. For OCP with a water getter inside (5% CaO) the side leakage can be monitored by the loss of scattering of the CaO when it reacts with water to Ca(OH)2. This work describes measurements of the rate of side leakage into the OCP layer of the TFE stack, both for plain OCP and for OCP with CaO getter inside. The side leakage curves are used to derive diffusion coefficients. Performing measurements at various climates provides acceleration factors that are relevant for the performance quantification of the TFE stack. The limiting factors on the performance of an unstructured TFE stack as produced in a roll-to-roll (R2R) process are presented. For small OLED devices side leakage would drastically reduce the shelf lifetime but for larger devices the permeation properties of the TFE stack determine the shelf lifetime.

A technique is presented on tracing the sub-micron pinholes that result in black spots in organic light-emitting diodes (OLED) when exposed to ambient atmosphere. The mystery about the type and nature of tiny pinholes present in the OLED cathode that allow oxygen and/or moisture ingress in minute quantities causing black spot formation, is clarified. The technique can accurately locate nanodefects or pinholes in the center of black spots of various sizes, even on a centimeter scale. Pinholes in the investigated OLEDs were shown to be caused by different particles originating from various locations in the device stack. Defects in the Ba-Al cathode of a solution processed polymer LED (PLED) and pinholes in the LiF-Al cathode of a thermally evaporated small molecule organic LED (smOLED) were investigated and compared. The technique is a powerful tool for inspection and can, thereby, accelerate the process optimization for OLED fabrication.

Organic light-emitting diodes degrade rapidly by means of local cathode oxidation when exposed to the ambient atmosphere, resulting in visible non-emissive areas called black spots. High performance inorganic based encapsulations are required to protect the OLED. We have applied a hybrid thin-film encapsulation stack consisting of two inorganic barrier layers of silicon nitride deposited at low temperature with an organic layer in between. The resulting water permeation mechanism into the OLED is solely by means of lateral pinhole-to-pinhole transport. With the application of CaO nanoparticles in the organic layer the lateral water transport rate is reduced and we show that black spot formation in 8 cm2 OLEDs is delayed by 6000 h at accelerated climate conditions of 60°C/90% relative humidity. This is estimated to correspond to 20 years at ambient conditions.

We present recent developments on flexible a-IGZO TFT technology scaling in terms of TFT channel length and operating voltage, as well as manufacturing cost optimization with a focus on R2R processing compatibility. We present progress on the relevant technology building blocks; (i) R2R compatible TFT architecture, (ii) (multilevel) nanoimprint lithography and (iii) S-ALD deposited TFT materials. Additionally, we show a developing application that drives scaling of the technology, namely a monolithically integrated flexible AMOLED display with in-display fingerprint detection.

Organic photodetectors (OPDs) have attracted much attention in recent years, due to their promise in large-area light sensing applications. Here, high-resolution slot-die-coated large-area bulk heterojunction organic photodiode (OPD) arrays are reported. The OPD uses a novel electron transport layer, indium gallium zinc oxide in combination with a molybdenum oxide top-electrode. Together, these effectively reduce dark current densities to very low levels of ≈10−7 mA cm−2 at −2 V. The OPDs show linear behavior in a wide range of light intensities and high detectivity values under reverse bias conditions. When coated on a 508 ppi TFT backplane, a high-quality optical fingerprint scanner capable of imaging in reflection is realized. The optical and electrical properties of the fingerprint sensor are characterized and high-resolution fingerprint images are obtained.

Because of their preferential two-dimensional layer-by-layer growth in thin films, 5,5'bis(4-alkylphenyl)-2,2'-bithiophenes (P2TPs) are model compounds for studying the effects of systematic chemical structure variations on thin-film structure and morphology, which in turn, impact the charge transport in organic field-effect transistors. For the first time, we observed, by grazing incidence X-ray diffraction (GIXD), a strong change in molecular tilt angle in a monolayer of P2TP, depending on whether the alkyl chain on the P2TP molecules was of odd or even length. The monolayers were deposited on densely packed ultrasmooth self-assembled alkane silane modified SiO2 surfaces. Our work shows that a subtle change in molecular structure can have a significant impact on the molecular packing structure in thin film, which in turn, will have a strong impact on charge transport of organic semiconductors. This was verified by quantum-chemical calculations that predict a corresponding odd-even effect in the strength of the intermolecular electronic coupling.

The availability of a high performance thin-film barrier is the most critical challenge in upscaling and commercializing flexible OLED products. We report a flexible thin-film-barrier technology that meets lifetime specifications for OLED lighting, and demonstrate it in rollable QVGA a-IGZO AMOLED displays. Roll-to-roll manufacturing of this high performance barrier film will be presented. cop. 2013 Society for Information Display.

Local laser ablation of the cathode of OLEDs has been applied to create a population of pinholes of the same size. This enables the direct comparison at different conditions of black spots and grey spots in the emission of OLEDs as a result of water ingress into the device. We confirmed earlier observations on the operational effect of black spot growth as determined in a sequential test on particle induced pinholes. Furthermore, we measured the operational effect in parallel, providing data that are test independent. With the same population of pinholes we studied the operational effect of grey spot growth. The observed larger operational effect of grey spot growth with respect to that of black spot growth is attributed to a lateral flow of protons to the centre of the black spot. In this part of the black spot a depletion region is present which is created by transport of H3O+ to the cathode under the influence of the applied electric field. This proposal is supported by the observation of black and grey spot growth in polymer LEDs on basis of PEDOT:PSS with increased pH.

To protect organic flexible devices from the ambient, they have to be encapsulated. Depending on the application in mind (OLED lighting, PV) different thin-film encapsulation methodology can be chosen. Each encapsulation process has different requirements and fabrication process freedom might be restricted, for example by mechanical reliability requirements or the total cost of the end product. Here we will show our recent investigations into different thin-film barriers with respect to their application and the route to production.

The crystalline film growth of TIPS-pentacene thin films by confined solution deposition is investigated. The crystalline thin films grow dendritic in the initial stage and continue to grow to elongated plate-like crystals when the solution is deposited in a confined space in-plane. The majority of the thin film, containing smaller thin crystals, is formed within the first 10 s after depositing the solution and continues to grow in minutes to millimeter sized single crystals. By atomic force microscopy we show that impurities are expelled by the growing crystals and clusters accumulate at step edges on the surface of the larger crystals. The influence of crystal thickness and orientation on the electronic transport in field-effect transistors is studied, and shows an optimum performance for devices with thin elongated crystals that are aligned parallel to the electric field between the source–drain electrodes.

Highly crystalline thin films of organic semiconductors processed from solution for electronic devices are difficult to achieve due to a slow and preferential three-dimensional growth of the crystals. Here we describe the development of a processing technique to induce a preferential two-dimensional crystalline growth of organic semiconductors by means of minimizing one dimension and confining the solution in two dimensions into a thin layer. The versatility of the process is demonstrated by processing small molecules (TIPS-pentacene and C 60 ) and a polymer (P3HT), all from solvents with a relatively low boiling point, to obtain crystalline thin films. The thin films show an improved in-plane packing of the molecules compared to films processed under similar conditions by spin coating, which is beneficial for the use in organic field-effect transistors.

Pentacene field-effect transistors were prepared on silicon nitride membranes for scanning transmission X-ray microscopy (STXM) investigations. The membranes were modified by different self-assembled monolayers (SAMs). Pentacene was deposited atop the SAM-treated membrane and the in-plane orientation of the grains were subsequently investigated by polarization dependent STXM measurements. The grain sizes were determined and compared to those obtained from atomic force microscopy (AFM) measurements. Statistical analysis of the grain orientation was correlated with the charge carrier mobility of the films, in which we observed an increase in the mobility with increasing grain size and decreasing surface roughness of the SAM.

5-Perfluorophenyl-11-phenyltetracene (FPPT) having both aryl (Ar) and perfluoroaryl (FAr) groups has been designed and synthesized to obtain well-defined π−π stacking structure of the tetracene core. Single-crystal X-ray analyses as well as photoconductivity and hole mobility measurements revealed that this strategy is promising for enhancement of the charge carrier properties.

By patterning a self-assembled monolayer (SAM) of thiolated molecules with opposing dipole moments on a gold anode of a polymer light-emitting diode (PLED), the charge injection and, therefore, the light-emission of the device can be controlled with a micrometer-scale resolution. Gold surfaces were modified with SAMs based on alkanethiols and perfluorinated alkanethiols, applied by microcontact printing, and their work functions have been measured. The molecules form a chemisorbed monolayer of only similar to 1.5 nm on the gold surface, thereby locally changing the work function of the metal. Kelvin probe measurements show that the local work function can be tuned from 4.3 to 5.5 eV, which implies that this anode can be used as a hole blocking electrode or as a hole injecting electrode, respectively, in PLEDs based on poly(p-phenylene vinylene) (PPV) derivatives. By microcontact printing of SAMs with opposing dipole moments, the work function was locally modified and the charge injection in the PLED could be controlled down to the micrometer length scale. Consequently, the local light-emission exhibits a high contrast. Microcontact printing of SAMs is a simple and inexpensive method to pattern, with micrometer resolution, the light-emission for low-end applications like static displays.

When organic light-emitting diodes (OLEDs) are exposed to the ambient atmosphere, water penetration through pinholes in the cathode results in the formation of non-emissive areas (black spots) due to local oxidation of the cathode around the pinhole. This degradation effect severely limits the lifetime of OLED devices and requires high performance encapsulation in order to delay its onset. We have investigated the process of degradation of OLED devices by water penetration through cathode pinholes, and have discovered that this is not just a simple oxidation of the cathode occurring as water diffuses within the device. We have observed that other layers within the device interact with the water. In solution processed OLEDs, the hole-injection layer (PEDOT:PSS) absorbs water due to the presence of the PSS acid (formation of H3O+). This results in a slight local reduction of the luminance of the device (grey spot) around the pinhole location and actually a reduction of the cathode black spot growth rate at the pinhole during a shelf lifetime test. When the device is not operated, the PEDOT:PSS layer is acting as a local reservoir for water keeping it away from the cathode and slowing down the cathode degradation. However, when the device is operated, water that is captured by the PEDOT:PSS layer to form H3O+ can be transported to the cathode under the influence of the applied electric field. This then increases the black spot growth rate. Experimental indications for this operational effect are provided by the threshold voltage behaviour of the effect and transient behaviour of the black spot growth after switching off the OLED. Direct evidence for the role of PEDOT:PSS in the operational effect has been provided by Raman Spectroscopy.

The use of molecular electronics is a much-discussed alternative to conventional silicon devices: the prospect of such tiny components has obvious implications for miniaturization. One approach is to replace the conventional semiconductor with a single molecular layer that self-organizes between two electrodes. Molecular tunnel junctions have been made in such systems, but they tend to be hard to reproduce, unstable and limited to small diameters. Now Akkerman et al. have developed a relatively simple way of producing stable, reproducible molecular junctions with large areas from self-assembled monolayers of alkanethiols. The process is compatible with standard integrated circuit technologies and could offer a cheap way forward in the quest for practical molecular electronics. A relatively simple method to fabricate stable, reproducible molecular junctions with large areas from self-assembled monolayers of alkanethiols has been developed — this approach could offer a cheap and promising way forward for molecular electronics. Electronic transport through single molecules has been studied extensively by academic1,2,3,4,5,6,7,8 and industrial9,10 research groups. Discrete tunnel junctions, or molecular diodes, have been reported using scanning probes11,12, break junctions13,14, metallic crossbars6 and nanopores8,15. For technological applications, molecular tunnel junctions must be reliable, stable and reproducible. The conductance per molecule, however, typically varies by many orders of magnitude5. Self-assembled monolayers (SAMs) may offer a promising route to the fabrication of reliable devices, and charge transport through SAMs of alkanethiols within nanopores is well understood, with non-resonant tunnelling dominating the transport mechanism8. Unfortunately, electrical shorts in SAMs are often formed upon vapour deposition of the top electrode16,17,18, which limits the diameter of the nanopore diodes to about 45 nm. Here we demonstrate a method to manufacture molecular junctions with diameters up to 100 µm with high yields (> 95 per cent). The junctions show excellent stability and reproducibility, and the conductance per unit area is similar to that obtained for benchmark nanopore diodes. Our technique involves processing the molecular junctions in the holes of a lithographically patterned photoresist, and then inserting a conducting polymer interlayer between the SAM and the metal top electrode. This simple approach is potentially low-cost and could pave the way for practical molecular electronics.

In this paper, we present some of the technology challenges and process temperature trade-offs when realizing AM OLED displays on thin flexible plastic films that can be mechanically bent to a roll radius of ∼1 cm. We furthermore present complementary approaches to realize low-power, high resolution OLED displays using self-aligned IGZO TFT architecture; a novel driving method using a compact 2T-1C pixel engine. cop. 2014 JSAP.

For organic semiconductors to find ubiquitous electronics applications, the development of new materials with high mobility and air stability is critical. Despite the versatility of carbon, exploratory chemical synthesis in the vast chemical space can be hindered by synthetic and characterization difficulties. Here we show that in silico screening of novel derivatives of the dinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene semiconductor with high hole mobility and air stability can lead to the discovery of a new high-performance semiconductor. On the basis of estimates from the Marcus theory of charge transfer rates, we identified a novel compound expected to demonstrate a theoretic twofold improvement in mobility over the parent molecule. Synthetic and electrical characterization of the compound is reported with single-crystal field-effect transistors, showing a remarkable saturation and linear mobility of 12.3 and 16 cm2 V−1 s−1, respectively. This is one of the very few organic semiconductors with mobility greater than 10 cm2 V−1 s−1 reported to date., The development of new organic semiconductors with high mobility and air stability will facilitate their widespread application. In this Article, in silico screening of extended oligothiophenes leads to the synthesis of a high performance semiconductor.

The charge transport properties critically depend on the degree of ordering of the chains in the solid state as well as on the density of chemical or structural defects. In general, goodelectronic performance requires strong electronic coupling between adjace nt molecules in the solid-state that yield strong intermolecular π-overlap. Herein, we newly designed and synthesized organic semiconducting materials having both aryl (Ar) and perfluoroaryl (FAr) as substituents for organic electronics along with molecular packing control. Regarding this molecular design, we hypothesized and expected that the Ar and FAr substituents would induce well-defined π-π stacking structure of charge transport units for high performance organic electronics devices.

The stability of molecular junctions is crucial for any application of molecular electronics. Degradation of molecular junctions when exposed to ambient conditions is regularly observed. In this report the stability of large-area molecular junctions under ambient conditions for more than two years is presented. Furthermore, the thermal stability of molecular junctions at elevated temperatures is investigated. A transition temperature at 50 degrees C was observed for molecular junctions based on self-assembled monolayers of alkanedithiols, above which the resistance decreases exponentially with temperature. This transition temperature limits the process window during fabrication and the temperature window during operation. (C) 2009 Elsevier B.V. All rights reserved.

A reliable and reproducible solid-state molecular electronic device that shows bidirectional conductance switching of molecular origin is demonstrated. The devices are manufactured by conventional processing techniques and are based on a molecular monolayer of photochromic diarylethenes, sandwiched between two electrodes, which switches reversibly and in situ between two conductance states via optical addressing.

A technology is demonstrated to fabricate reliable metal-molecule-metal junctions with unprecedented device diameters up to 100 μm. The yield of these molecular junctions is close to unity. Preliminary stability investigations have shown a shelf life of years and no deterioration upon cycling. Key ingredients are the use of a conducting polymer layer (PEDOT:PSS) sandwiched between a bottom electrode with a self-assembled monolayer (SAM) and the top electrode to prevent electrical shorts, and processing in lithographically defined vertical interconnects (vias) to prevent both parasitic currents and interaction between the environment and the SAM [1].Modeling the current–voltage (I–V) characteristics of alkanedithiols with the Simmons model showed that the low dielectric constant of the molecules in the junction results in a strong image potential that should be included in the tunneling model. Including image force effects, the tunneling model consistently describes the current-voltage characteristics of the molecular junctions up to 1 V bias for different molecule lengths [2].Furthermore, we demonstrate a dependence of the I–V characteristics on the monolayer quality. A too low concentration of long alkanedithiols leads to the formation of looped molecules, resulting in a 50-fold increase of the current through the SAM. To obtain an almost full standing-up phase of 1,14-tetradecanedithiol (C14) a 30 mM concentration is required, whereas a 0.3 mM concentration leads to a highly looped monolayer. The conduction through the full standing-up phase of C14 and C16 is in accordance with the exponential dependence on molecular length as obtained from shorter alkanedithiols [3].Finally, a fully functional solid-state molecular electronic switch is manufactured by conventional processing techniques. The molecular switch is based on a monolayer of photochromic diarylethene molecular switches. The monolayer reversibly switches the conductance by more than one order of magnitude between the two conductance states via optical addressing. This reversible conductance switch operates as an electronic ON/OFF switch (or a reprogrammable data storage unit) that can be optically written and electronically read [4].

The orientation of alkanedithiol molecules in self-assembled monolayers (SAMs) is of vital importance for their transport properties in molecular junctions. It is demonstrated that a too-low concentration of long alkanedithiols in ethanol leads to the formation of looped molecules, resulting in a 50-fold increase of the current through the SAM. X-ray photoelectron spectroscopy measurements show that high-concentration dithiol solutions result in a preferential standing-up phase. To obtain an almost full standing-up phase of 1,14-tetradecanedithiol (C14) a 30 mM concentration in ethanol is required, whereas a 0.3 mM concentration leads to a highly looped monolayer. The conduction through the full standing-up phase of C14 and C16 is in accordance with the exponential dependence on molecule length as obtained from shorter alkanedithiols.

The electrical transport through self-assembled monolayers of alkanedithiols was studied in large-area molecular junctions and described by the Simmons model [Simmons JG (1963) J Appl Phys 34:1793–1803 and 2581–2590] for tunneling through a practical barrier, i.e., a rectangular barrier with the image potential included. The strength of the image potential depends on the value of the dielectric constant. A value of 2.1 was determined from impedance measurements. The large and well defined areas of these molecular junctions allow for a simultaneous study of the capacitance and the tunneling current under operational conditions. Electrical transport for octanedithiol through tetradecanedithiol self-assembled monolayers up to 1 V can simultaneously be described by a single effective mass and a barrier height. There is no need for additional fit constants. The barrier heights are in the order of 4–5 eV and vary systematically with the length of the molecules. Irrespective of the length of the molecules, an effective mass of 0.28 was determined, which is in excellent agreement with theoretical predictions.