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Charge Carrier Mobility (charge + carrier_mobility)
Selected AbstractsModeling Polymer Dielectric/Pentacene Interfaces: On the Role of Electrostatic Energy Disorder on Charge Carrier MobilityADVANCED FUNCTIONAL MATERIALS, Issue 20 2009Nicolas G. Martinelli Abstract Force-field and quantum-chemical calculations are combined to model the packing of pentacene molecules at the atomic level on two polymer dielectric layers (poly(methyl methacrylate) (PMMA) versus polystyrene (PS)) widely used in field-effect transistors and to assess the impact of electrostatic interactions at the interface on the charge mobility values in the pentacene layers. The results show unambiguously that the electrostatic interactions introduce a significant energetic disorder in the pentacene layer in contact with the polymer chains; a drop in the hole mobility by a factor of 5 is predicted with PS chains while a factor of 60 is obtained for PMMA due to the presence of polar carbonyl groups. [source] Potentiometry on pentacene OFETs: Charge carrier mobilities and injection barriers in bottom and top contact configurationsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 3 2008R. Scholz Abstract In a combination of experimental techniques including electrical probes, potentiometry, and charge transient spectroscopy (QTS), we develop concepts how to quantify the potential drops at the contacts, the mobility in the channel region, and the density of states of deep traps in pentacene OFETs. For OFETs grown from unpurified pentacene on pre-patterned Au bottom contacts, a comparison between potentiometry and two-dimensional device simulations determines an injection barrier of 0.73 eV at the source contact and a hole mobility of 0.014 cm2 V,1 s,1 in the pentacene channel. Temperature-dependent QTS data reveal a trap level at about 125 meV from the hole transport band, indicating a relatively high density of unintentional dopants and therefore a high background density of majority charge carriers. In OFETs grown from purified pentacene onto a SiO2 gate dielectric and Au top contacts evaporated onto the pentacene channel without breaking the vacuum, potentiometry reveals a nearly perfect alignment of the metal work function with the hole transport level in the organic layer. The much lower density of deep traps in these samples raises the hole mobility to the range 0.1,0.2 cm2 V,1 s,1. A further improvement of the hole mobility and the resulting device performance can be achieved by a chemical treatment of the gate oxide with n-octadecytrichlorosilane (OTS). (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Temperature-Resolved Local and Macroscopic Charge Carrier Transport in Thin P3HT Layers,ADVANCED FUNCTIONAL MATERIALS, Issue 14 2010Patrick Pingel Abstract Previous investigations of the field-effect mobility in poly(3-hexylthiophene) (P3HT) layers revealed a strong dependence on molecular weight (MW), which was shown to be closely related to layer morphology. Here, charge carrier mobilities of two P3HT MW fractions (medium-MW: Mn,=,7,200 g mol,1; high-MW: Mn,=,27,000 g mol,1) are probed as a function of temperature at a local and a macroscopic length scale, using pulse-radiolysis time-resolved microwave conductivity (PR-TRMC) and organic field-effect transistor measurements, respectively. In contrast to the macroscopic transport properties, the local intra-grain mobility depends only weakly on MW (being in the order of 10,2 cm2 V,1 s,1) and being thermally activated below the melting temperature for both fractions. The striking differences of charge transport at both length scales are related to the heterogeneity of the layer morphology. The quantitative analysis of temperature-dependent UV/Vis absorption spectra according to a model of F. C. Spano reveals that a substantial amount of disordered material is present in these P3HT layers. Moreover, the analysis predicts that aggregates in medium-MW P3HT undergo a "pre-melting" significantly below the actual melting temperature. The results suggest that macroscopic charge transport in samples of short-chain P3HT is strongly inhibited by the presence of disordered domains, while in high-MW P3HT the low-mobility disordered zones are bridged via inter-crystalline molecular connections. [source] Transistor Paint: Environmentally Stable N -alkyldithienopyrrole and Bithiazole-Based Copolymer Thin-Film Transistors Show Reproducible High Mobilities without AnnealingADVANCED FUNCTIONAL MATERIALS, Issue 21 2009Junying Liu Abstract New solution processable 4-(2-hexyldecan)- 4H -bisthieno[2,3- d:3,,2,- b]pyrrole and 4,4,-dialkyl-2,2,-bithiazole-based copolymers (PBTzDTPs) are synthesized with excellent FET performance. These novel copolymers have considerable potential in printable electronics as they have high charge carrier mobilities, excellent air stability, good solution processibility, and no requirement for post-deposition thermal annealing, all requirements for this field of application. The thin film transistors fabricated from PBTzDTPs achieve field effect mobilities as high as 0.14,cm2 V,1 s,1 with current on/off ratios up to 106 without thermal annealing. In addition, the devices exhibit stable performance in air, showing no significant degradation over 60 days. Moreover, the polymers described here provide an excellent example of the systems in which higher mobility performance does not require higher crystalline, long-range ordered structures. Such a system appears to be particularly promising for rapid fabrication techniques, where kinetic conditions usually prevent the development of long-range order. [source] Semiconducting Thienothiophene Copolymers: Design, Synthesis, Morphology, and Performance in Thin-Film Organic TransistorsADVANCED MATERIALS, Issue 10-11 2009Iain McCulloch Abstract Organic semiconductors are emerging as a viable alternative to amorphous silicon in a range of thin-film transistor devices. With the possibility to formulate these p-type materials as inks and subsequently print into patterned devices, organic-based transistors offer significant commercial advantages for manufacture, with initial applications such as low performance displays and simple logic being envisaged. Previous limitations of both air stability and electrical performance are now being overcome with a range of both small molecule and polymer-based solution-processable materials, which achieve charge carrier mobilities in excess of 0.5,cm2 V,1 s,1, a benchmark value for amorphous silicon semiconductors. Polymer semiconductors based on thienothiophene copolymers have achieved amongst the highest charge carrier mobilities in solution-processed transistor devices. In this Progress Report, we evaluate the advances and limitations of this class of polymer in transistor devices. [source] High-Performance Polymer-Small Molecule Blend Organic TransistorsADVANCED MATERIALS, Issue 10-11 2009Richard Hamilton A double-gate device is used to demonstrate that a blended formulation of semiconducting small molecules and a polymer matrix can provide high electrical performance within thin-film field-effect transistors (OTFTs) with charge carrier mobilities of greater than 2,cm2,V,1,s,1, good device-to-device uniformity, and the potential to fabricate devices from routine printing techniques. [source] Liquid Crystalline Ordering and Charge Transport in Semiconducting MaterialsMACROMOLECULAR RAPID COMMUNICATIONS, Issue 14 2009Wojciech Pisula Abstract Organic semiconducting materials offer the advantage of solution processability into flexible films. In most cases, their drawback is based on their low charge carrier mobility, which is directly related to the packing of the molecules both on local (amorphous versus crystalline) and on macroscopic (grain boundaries) length scales. Liquid crystalline ordering offers the possibility of circumventing this problem. An advanced concept comprises: i) the application of materials with different liquid crystalline phases, ii) the orientation of a low viscosity high temperature phase, and, iii) the transfer of the macroscopic orientation during cooling to a highly ordered (at best, crystalline-like) phase at room temperature. At the same time, the desired orientation for the application (OLED or field-effect transistor) can be obtained. This review presents the use of molecules with discotic, calamitic and sanidic phases and discusses the sensitivity of the phases with regard to defects depending on the dimensionality of the ordered structure (columns: 1D, smectic layers and sanidic phases: 2D). It presents ways to systematically improve charge carrier mobility by proper variation of the electronic and steric (packing) structure of the constituting molecules and to reach charge carrier mobilities that are close to and comparable to amorphous silicon, with values of 0.1 to 0.7,cm2,·,V,1,·,s,1. In this context, the significance of cross-linking to stabilize the orientation and liquid crystalline behavior of inorganic/organic hybrids is also discussed. [source] Dielectric layers for organic field effect transistors as gate dielectric and surface passivationPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 3 2008T. Diekmann Abstract Organic field effect transistors with the organic semiconductor pentacene, using silicon substrates, were successfully built on conventional inorganic dielectrics like silicon dioxide or silicon nitride. They can drive drain currents up to 15 mA. Beyond that, polymer films were investigated as gate dielectrics in order to achieve transistors on plastic films. On polyester substrates with an inorganic,organic gate dielectric, devices reach drain currents comparable to transistors on silicon dioxide and charge carrier mobilities of up to 0.35 cm2/V s. Analysis of the pentacene surface by atomic force microscopy showed pentacene crystallites achieving dimensions of more than 1.5 µm. The unprotected organic devices suffer from degradation due to water and oxygen incorporation. Therefore, the application of a hydrophobic polytetrafluoroethylene layer as capping layer is studied. Because of the reduced influence of water, a shift to positive threshold voltages is caused. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Tetrachloro-substituted Perylene Bisimide Dyes as Promising n-Type Organic Semiconductors: Studies on Structural, Electrochemical and Charge Transport PropertiesCHEMPHYSCHEM, Issue 1 2004Zhijian Chen Twisted ,-systems: The highly twisted 1,6,7,12-tetrachloro-substituted perylene bisimides possess an improved electron affinity. The nonplanar nature of these molecules facilitates a slipped brickstone-type rather than a columnar stacking of the ,-systems, with a potentially useful two dimensional contact feature. These compounds show isotropic charge carrier mobilities as high as up to 0.14 cm2,V,1 s,1 (see graphic). [source] Solution Processable Fluorenyl Hexa- peri -hexabenzocoronenes in Organic Field-Effect Transistors and Solar CellsADVANCED FUNCTIONAL MATERIALS, Issue 6 2010Wallace W. H. Wong Abstract The organization of organic semiconductor molecules in the active layer of organic electronic devices has important consequences to overall device performance. This is due to the fact that molecular organization directly affects charge carrier mobility of the material. Organic field-effect transistor (OFET) performance is driven by high charge carrier mobility while bulk heterojunction (BHJ) solar cells require balanced hole and electron transport. By investigating the properties and device performance of three structural variations of the fluorenyl hexa- peri -hexabenzocoronene (FHBC) material, the importance of molecular organization to device performance was highlighted. It is clear from 1H NMR and 2D wide-angle X-ray scattering (2D WAXS) experiments that the sterically demanding 9,9-dioctylfluorene groups are preventing ,,, intermolecular contact in the hexakis-substituted FHBC 4. For bis-substituted FHBC compounds 5 and 6, ,,, intermolecular contact was observed in solution and hexagonal columnar ordering was observed in solid state. Furthermore, in atomic force microscopy (AFM) experiments, nanoscale phase separation was observed in thin films of FHBC and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) blends. The differences in molecular and bulk structural features were found to correlate with OFET and BHJ solar cell performance. Poor OFET and BHJ solar cells devices were obtained for FHBC compound 4 while compounds 5 and 6 gave excellent devices. In particular, the field-effect mobility of FHBC 6, deposited by spin-casting, reached 2.8,×,10,3,cm2 V,1 s and a power conversion efficiency of 1.5% was recorded for the BHJ solar cell containing FHBC 6 and PC61BM. [source] Ionic Iridium(III) Complexes with Bulky Side Groups for Use in Light Emitting Cells: Reduction of Concentration QuenchingADVANCED FUNCTIONAL MATERIALS, Issue 13 2009Carsten Rothe Abstract Here, the photophysics and performance of single-layer light emitting cells (LECs) based on a series of ionic cyclometalated Ir(III) complexes of formulae and where ppy, bpy, and phen are 2-phenylpyridine, substituted bipyridine and substituted phenanthroline ligands, respectively, are reported. Substitution at the N,N ligand has little effect on the emitting metal-ligand to ligand charge-transfer (MLLCT) states and functionalization at this site of the complex leads to only modest changes in emission color. For the more bulky complexes the increase in intermolecular separation leads to reduced exciton migration, which in turn, by suppressing concentration quenching, significantly increases the lifetime of the excited state. On the other hand, the larger intermolecular separation induced by bulky ligands reduces the charge carrier mobility of the materials, which means that higher bias fields are needed to drive the diodes. A brightness of ca. 1000,cd,m,2 at 3,V is obtained for complex 5, which demonstrates a beneficial effect of bulky substituents. [source] A Densely and Uniformly Packed Organic Semiconductor Based on Annelated , -Trithiophenes for High-Performance Thin Film TransistorsADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Lin Tan Abstract A novel semiconductor based on annelated , -trithiophenes is presented, possessing an extraordinary compressed packing mode combining edge-to-face ,,, interactions and S,S interactions in single crystals, which is favorable for more effective charge transporting. Accordingly, the device incorporating this semiconductor shows remarkably high charge carrier mobility, as high as 0.89,cm2,V,1,s,1, and an on/off ratio of 4.6,×,107 for vacuum-deposited thin films. [source] Orders-of-Magnitude Reduction of the Contact Resistance in Short-Channel Hot Embossed Organic Thin Film Transistors by Oxidative Treatment of Au-Electrodes,ADVANCED FUNCTIONAL MATERIALS, Issue 15 2007B. Stadlober Abstract In this study we report on the optimization of the contact resistance by surface treatment in short-channel bottom-contact OTFTs based on pentacene as semiconductor and SiO2 as gate dielectric. The devices have been fabricated by means of nanoimprint lithography with channel lengths in the range of 0.3,,m,<,L,<,3.0,,m. In order to reduce the contact resistance the Au source- and drain-contacts were subjected to a special UV/ozone treatment, which induced the formation of a thin AuOx layer. It turned out, that the treatment is very effective (i),in decreasing the hole-injection barrier between Au and pentacene and (ii),in improving the morphology of pentacene on top of the Au contacts and thus reducing the access resistance of carriers to the channel. Contact resistance values as low as 80,,,cm were achieved for gate voltages well above the threshold. In devices with untreated contacts, the charge carrier mobility shows a power-law dependence on the channel length, which is closely related to the contact resistance and to the grain-size of the pentacene crystallites. Devices with UV/ozone treated contacts of very low resistance, however, exhibit a charge carrier mobility in the range of 0.3,cm2,V,1,s,1,<,,,<,0.4,cm2,V,1,s,1 independent of the channel length. [source] High-Performance Single Crystal Organic Field-Effect Transistors Based on Two Dithiophene-Tetrathiafulvalene (DT-TTF) PolymorphsADVANCED MATERIALS, Issue 37 2010Raphael Pfattner Solution prepared single crystal organic field-effect transistors (OFETs) combine low-cost with high performance due to structural ordering of molecules. However, in organic crystals polymorphism is a known phenomenon, which can have a crucial influence on charge transport. Here, the performance of solution-prepared single crystal OFETs based on two different polymorphs of dithiophene-tetrathiafulvalene, which were investigated by confocal Raman spectroscopy and X-ray diffraction, are reported. OFET devices prepared using different configurations show that both polymorphs exhibited excellent device performance, although the ,-phase revealed charge carrier mobility between two and ten times higher in accordance to the closer stacking of the molecules. [source] Silicon Nanowires: A Review on Aspects of their Growth and their Electrical PropertiesADVANCED MATERIALS, Issue 25-26 2009Volker Schmidt Abstract This paper summarizes some of the essential aspects of silicon-nanowire growth and of their electrical properties. In the first part, a brief description of the different growth techniques is given, though the general focus of this work is on chemical vapor deposition of silicon nanowires. The advantages and disadvantages of the different catalyst materials for silicon-wire growth are discussed at length. Thereafter, in the second part, three thermodynamic aspects of silicon-wire growth via the vapor,liquid,solid mechanism are presented and discussed. These are the expansion of the base of epitaxially grown Si wires, a stability criterion regarding the surface tension of the catalyst droplet, and the consequences of the Gibbs,Thomson effect for the silicon wire growth velocity. The third part is dedicated to the electrical properties of silicon nanowires. First, different silicon nanowire doping techniques are discussed. Attention is then focused on the diameter dependence of dopant ionization and the influence of interface trap states on the charge carrier density in silicon nanowires. It is concluded by a section on charge carrier mobility and mobility measurements. [source] A Nitrogen Dioxide Sensor Based on an Organic Transistor Constructed from Amorphous Semiconducting Polymers,ADVANCED MATERIALS, Issue 22 2007A. Das Organic field effect transistors based on amorphous semiconducting polymers are used as highly effective sensors for the detection of low concentrations of NO2. The figure shows the experimental setup used to detect the toxic odor. The threshold voltage rather than the charge carrier mobility is seen to be greatly modified by exposure to NO2. [source] Liquid Crystalline Ordering and Charge Transport in Semiconducting MaterialsMACROMOLECULAR RAPID COMMUNICATIONS, Issue 14 2009Wojciech Pisula Abstract Organic semiconducting materials offer the advantage of solution processability into flexible films. In most cases, their drawback is based on their low charge carrier mobility, which is directly related to the packing of the molecules both on local (amorphous versus crystalline) and on macroscopic (grain boundaries) length scales. Liquid crystalline ordering offers the possibility of circumventing this problem. An advanced concept comprises: i) the application of materials with different liquid crystalline phases, ii) the orientation of a low viscosity high temperature phase, and, iii) the transfer of the macroscopic orientation during cooling to a highly ordered (at best, crystalline-like) phase at room temperature. At the same time, the desired orientation for the application (OLED or field-effect transistor) can be obtained. This review presents the use of molecules with discotic, calamitic and sanidic phases and discusses the sensitivity of the phases with regard to defects depending on the dimensionality of the ordered structure (columns: 1D, smectic layers and sanidic phases: 2D). It presents ways to systematically improve charge carrier mobility by proper variation of the electronic and steric (packing) structure of the constituting molecules and to reach charge carrier mobilities that are close to and comparable to amorphous silicon, with values of 0.1 to 0.7,cm2,·,V,1,·,s,1. In this context, the significance of cross-linking to stabilize the orientation and liquid crystalline behavior of inorganic/organic hybrids is also discussed. [source] Influence of charge carrier mobility on the performance of organic solar cellsPHYSICA STATUS SOLIDI - RAPID RESEARCH LETTERS, Issue 4 2008Carsten Deibel Abstract The power conversion efficiency of organic solar cells based on donor,acceptor blends is governed by an interplay of polaron pair dissociation and bimolecular polaron recombination. Both processes are strongly dependent on the charge carrier mobility, the dissociation increasing with faster charge transport, with raised recombination losses at the same time. Using a macroscopic effective medium simulation, we calculate the optimum charge carrier mobility for the highest power conversion efficiency, for the first time accounting for injection barriers and a reduced Langevin-type recombination. An enhancement of the charge carrier mobility from 10,8 m2/V s for state of the art polymer,fullerene solar cells to about 10,6 m2/V s, which yields the maximum efficiency, corresponds to an improvement of only about 20% for the given parameter set. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Amorphous films of tris(8-hydroxyquinolinato)aluminium: Force-field, morphology, and charge transportPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 12 2009Alexander Lukyanov Abstract The effect of the force-field parameters on the morphology and charge dynamics is assessed for amorphous films of tris(8-hydroxyquinolinato)aluminium. Two force-fields are used for non-bonded parameters, OPLS and Williams 99, whereas bonded interactions are obtained from first-principles calculations. By comparing densities and glass transition temperatures we conclude that the OPLS-based force field provides a better description of the amorphous morphology. At the same time, the difference in molecular packing does not significantly affect the distribution of charge hopping rates or charge carrier mobility. [source] Special issue: Physics of Organic SemiconductorsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2004Wolfgang Brütting This special issue of physica status solidi (a) gives an overview of our present-day knowledge of the physics behind organic semiconductor devices, ranging from the growth of organic layers and crystals, their electronic properties at interfaces, their photophysics and electrical transport properties to the application in organic field-effect transistors, photovoltaic cells and organic light-emit-ting diodes. Guest Editor of the present issue is Wolfgang Brütting, professor at the University of Augsburg, where he leads a research group working on organic semiconductors, their physical and materials properties, and the understanding of the basic processes in these materials and devices. The cover picture is an angular plot of the anisotropy of the charge carrier mobility , in the a,b plane of a rubrene single crystal, probed on an elastomeric rubber stamp field-effect transistor device. The black and red squares correspond to the values of , extracted from the linear and saturation regimes of the transistor operation, respectively. More information can be found in the Review Article by R. W. I. de Boer et al. [1]. [source] Measuring carrier mobility in conventional multilayer organic light emitting devices by delayed exciton generationPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 5 2008S. Reineke Abstract The authors present an alternative method for the determination of the charge carrier mobility of organic thin films. In contrast to known methods like space charge limited current, field effect transistor and time of flight approaches, we determine the charge carrier mobility of a mixed film, serving as emission layer, within the conventional multilayer device architecture. We make use of a strong delayed generation feature in the electroluminescent decay, following a short voltage pump pulse in a time-resolved set-up. Taking into account the preferentially electron transporting properties of the film, the mobility of a N,N ,-di(naphthalen-2-yl)- N,N ,-diphenyl-benzidine (NPB):tris(1-phenylisoquinoline) iridium [Ir(piq)3] mixed film is found to be on the order of 10,5 cm2 (Vs),1. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Model of the influence of energetic disorder on inter-chain charge carrier mobility in poly[2-methoxy-5-(2,-ethylhexyloxy)- p -phenylene vinylene]POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 3 2009Petr Toman Abstract The theoretical model of the inter-chain charge carrier mobility in poly[2-methoxy-5-(2,-ethylhexyloxy)- p -phenylene vinylene] (MEH,PPV) doped with polar additive is put forward. The polymer chain states of a charge carrier were calculated by means of diagonalization of a tight-binding Hamiltonian, which includes disorder in both the local energies and transfer integrals. Consequently, the inter-chain charge carrier transport is taking place on a spatially and energetically disordered medium. Because it is believed that the additive does not significantly influence the polymer supramolecular structure, the polymer conformations were simplified as much as possible. On the other hand, the energetic disorder is rigorously described. The transfer rates between the polymer chains were determined using the quasi-classical Marcus theory. The model considered the following steps of the charge carrier transport: the charge carrier hops to a given polymer chain. Then, the charge carrier thermalizes to the Boltzmann distribution over all its possible states on this chain. After that, the charge carrier hops to any possible state on one of the four nearest neighboring chains. The results showed that the inter-chain charge carrier mobility is very strongly dependent on the degree of the energetic disorder. If the energetic disorder is doubled from 0.09 to 0.18,eV, the mobility decreases by two or three orders of magnitude. Copyright © 2008 John Wiley & Sons, Ltd. [source] A review of charge transport and recombination in polymer/fullerene organic solar cellsPROGRESS IN PHOTOVOLTAICS: RESEARCH & APPLICATIONS, Issue 8 2007A. Pivrikas Abstract The charge carrier transport and recombination in two types of thermally treated bulk-heterojunction solar cells is reviewed: in regioregular poly(3-hexylthiophene) (RRP3HT) mixed with 1-(3-methoxycarbonyl)propyl-1-phenyl-[6,6]-methanofullerene (PCBM) and in the blend of poly[2-methoxy-5-(3,7-dimethyloctyloxy)-phenylene vinylene] (MDMO-PPV) mixed with PCBM. The charge carrier mobility and bimolecular recombination coefficient have been comparatively studied by using various techniques including Time-of-Flight (ToF), Charge Extraction by Linearly Increasing Voltage (CELIV), Double Injection (DI) transients, Current,Voltage (I,V) technique. It was found that the carrier mobility is at least an order of magnitude higher in RRP3HT/PCBM blends compared to MDMO-PPV/PCBM. Moreover, all used techniques demonstrate a heavily reduced charge carrier recombination in RRP3HT/PCBM films compared to Langevin-type carrier bimolecular recombination in MDMO-PPV/PCBM blends. As a result of long carrier lifetimes the formation of high carrier concentration plasma in RRP3HT/PCBM blends is demonstrated and plasma extraction methods were used to directly estimate the charge carrier mobility and bimolecular recombination coefficients simultaneously. A weak dependence of bimolecular recombination coefficient on the applied electric field and temperature demonstrates that carrier recombination is not dominated by charge carrier mobility (Langevin-type recombination) in RRP3HT/PCBM blends. Furthermore, we found from CELIV techniques that electron mobility in RRP3HT/PCBM blends is independent on relaxation time in the experimental time window (approx. hundreds of microseconds to tens of milliseconds). This reduced carrier bimolecular recombination in RRP3HT/PCBM blends implies that the much longer carrier lifetimes can be reached at the same concentrations which finally results in higher photocurrent and larger power conversion efficiency of RRP3HT/PCBM solar cells. Copyright © 2007 John Wiley & Sons, Ltd. [source] Theoretical Characterization of Charge Transport in One-Dimensional Collinear Arrays of Organic Conjugated MoleculesCHEMPHYSCHEM, Issue 5 2010Lucas Viani Abstract A great deal of interest has recently focused on host,guest systems consisting of one-dimensional collinear arrays of conjugated molecules encapsulated in the channels of organic or inorganic matrices. Such architectures allow for controlled charge and energy migration processes between the interacting guest molecules and are thus attractive in the field of organic electronics. In this context, we characterize here at a quantum-chemical level the molecular parameters governing charge transport in the hopping regime in 1D arrays built with different types of molecules. We investigate the influence of several parameters (such as the symmetry of the molecule, the presence of terminal substituents, and the molecular size) and define on that basis the molecular features required to maximize the charge carrier mobility within the channels. In particular, we demonstrate that a strong localization of the molecular orbitals in push,pull compounds is generally detrimental to the charge transport properties. [source] | ||||||||||||||||