Efficient and bright polymer light emitting field effect transistors

Light emitting field effect transistors (LEFETs) are emerging as a multi-functional class of optoelectronic devices. LEFETs can simultaneously execute light emission and the standard logic functions of a transistor in a single architecture. However, current LEFET architectures deliver either high brightness or high efficiency but not both concurrently, thus limiting their use in technological applications. Here we show an LEFET device strategy that simultaneously improves brightness and efficiency. The key step change in LEFET performance arises from the bottom gate top-contact device architecture in which the source/drain electrodes are semitransparent and the active channel contains a bi-layer comprising of a high mobility charge-transporting polymer, and a yellow–green emissive polymer. A record external quantum efficiency (EQE) of 2.1% at 1000 cd/m² is demonstrated for polymer based bilayer LEFETs.     

Solution‐Processed Zinc Oxide as High‐Performance Air‐Stable Electron Injector in Organic Ambipolar Light‐Emitting Field‐Effect Transistors

Electron injection from the source–drain electrodes limits the performance of many n‐type organic field‐effect transistors (OFETs), particularly those based on organic semiconductors with electron affinities less than 3.5 eV. Here, it is shown that modification of gold source–drain electrodes with an overlying solution‐deposited, patterned layer of an n‐type metal oxide such as zinc oxide (ZnO) provides an efficient electron‐injecting contact, which avoids the use of unstable low‐work‐function metals and is compatible with high‐resolution patterning techniques such as photolithography. Ambipolar light‐emitting field‐effect transistors (LEFETs) based on green‐light‐emitting poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT) and blue‐light‐emitting poly(9,9‐dioctylfluorene) (F8) with electron‐injecting gold/ZnO and hole‐injecting gold electrodes show significantly lower electron threshold voltages and several orders of magnitude higher ambipolar currents, and hence light emission intensities, than devices with bare gold electrodes. Moreover, different solution‐deposited metal oxide injection layers are compared. By spin‐coating ZnO from a low‐temperature precursor, processing temperatures could be reduced to 150 °C. Ultraviolet photoemission spectroscopy (UPS) shows that the improvement in transistor performance is due to reduction of the electron injection barrier at the interface between the organic semiconductor and ZnO/Au compared to bare gold electrodes.     

En Route to Wide Area Emitting Organic Light-Emitting Transistors for Intrinsic Drive-Integrated Display Applications: A Comprehensive Review

Organic light-emitting transistors (OLET) evolved from the fusion of the switching functionality of field-effect transistors (FET) with the light-emitting characteristics of organic light-emitting diode (OLED) that can simplify the active-matrix pixel device architecture and hence offer a promising pathway for future flat panel and flexible display technology. This review systematically analyzes the key device/molecular engineering tactics that assist in improving the electrode edge narrow emission to wide-area emission for display applications via three different topics, that is, narrow to wide-area emission, vertical architecture, and impact of high-κ dielectric on the device performance. Source–drain electrode engineering such as symmetric/asymmetric, planar/non-planar arrangement, semitransparent nature, multilayer approach comprising charge transport, and work function modification layers enable widening the emission zone. Vertical OLET architecture offers short channel lengths with a high aperture ratio, pixel type area emission, and stable light-emitting area. Transistors utilizing high-κ dielectric materials have assisted in lowering the operating voltage, enhancing luminance and air stability. The promising development in achieving wide-area emission provides a solid basis for constructing OLET research toward display applications; however, it relies on developing highly luminescent and fast charge transporting materials, suitable semitransparent source/drain electrodes, high-κ -dielectrics, and device architectural engineering.     

Integration of a Rib Waveguide Distributed Feedback Structure into a Light‐Emitting Polymer Field‐Effect Transistor

Ambipolar light‐emitting organic field‐effect transistors (LEFETs) possess the ability to efficiently emit light due to charge recombination in the channel. Since the emission can be made to occur far from the metal electrodes, the LEFET structure has been proposed as a potential architecture for electrically pumped organic lasers. Here, a rib waveguide distributed feedback structure consisting of tantalum pentoxide (Ta₂O₅) integrated within the channel of a top gate/bottom contact LEFET based on poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT) is demonstrated. The emitted light is coupled efficiently into the resonant mode of the DFB waveguide when the recombination zone of the LEFET is placed directly above the waveguide ridge. This architecture provides strong mode confinement in two dimensions. Mode simulations are used to optimize the dielectric thickness and gate electrode material. It is shown that electrode absorption losses within the device can be eliminated and that the lasing threshold for optical pumping of the LEFET structure with all electrodes (4.5 µJ cm^?2) is as low as that of reference devices without electrodes. These results enable quantitative judgement of the prospects for realizing an electrically pumped organic laser based on ambipolar LEFETs. The proposed device provides a powerful, low‐loss architecture for integrating high‐performance ambipolar organic semiconductor materials into electrically pumped lasing structures.     

Quantum Dot Light‐Emitting Transistors—Powerful Research Tools and Their Future Applications

In this progress report, the recent work in the field of light‐emitting field‐effect transistors (LEFETs) based on colloidal quantum dots (CQDs) as emitters is highlighted. These devices combine the possibility of electrical switching, as known from field‐effect transistors, with the possibility of light emission in a single device. The properties of field‐effect transistors and the prerequisites of LEFETs are reviewed, before motivating the use of colloidal quantum dots for light emission. Recent reports on these quantum dot light‐emitting field‐effect transistors (QDLEFETs) include both materials emitting in the near infrared and the visible spectral range—underlining the great potential and breadth of applications for QDLEFETs. The way in which LEFETs can further the understanding of the CQD material properties—their photophysics as well as the carrier transport through films—is discussed. In addition, an overview of technology areas offering the potential for large impact is provided.     

Organic Light‐Emitting Transistors Containing a Laterally Arranged Heterojunction

An approach to produce organic light‐emitting transistors (OLETs) containing a laterally arranged heterojunction structure, which minimizes exciton quenching at the metal electrodes, is described. This device configuration provides an organic light‐emitting diode (OLED) structure where the anode (source) electrode, hole‐transport material (field‐effect material), light‐emitting material, and cathode (drain) electrode are laterally arranged, thus offering a chance to control the electroluminescent intensity by changing the gate bias. Pentacene and tris(8‐quinolinolato)aluminum (Alq₃) are employed as the field‐effect and light‐emitting materials, respectively. The laterally arranged heterojunction structures are achieved by successively inclined deposition of the field‐effect and light‐emitting materials. After deposition of pentacene, a narrow gap of about 10–20 nm between the drain electrode and pentacene was obtained, thereby creating an opportunity to fabricate a laterally arranged heterojunction. In the OLETs, unsymmetrical source and drain electrodes, that is, Au and LiF/Al ones, are used to ensure efficient injection of holes and electrons. Visible‐light emission from OLETs is observed under ambient atmosphere. This result is ascribed to efficient carrier injection and transport, formation of a heterojunction, as well as good luminescence from the organic emissive layer. The device structure serves as an excellent model system for OLETs and demonstrates a general concept of adjusting the charge‐carrier injection and transport, as well as the electroluminescent properties, by forming laterally arranged heterojunctions.     

Recent Developments and Novel Applications of Thin Film,Light‐Emitting Transistors

Light‐emitting field‐effect transistors (LEFETs) combine switching and amplification with light emission and thus represent an interesting optoelectronic device. They are not limited anymore to a few examples and specific materials but are nearly universal for a wide range of semiconductors, from organic to inorganic and nanoscale. This review introduces the basic working principles of lateral unipolar and ambipolar LEFETs and discusses recent examples based on various solution‐processed semiconducting materials. Applications beyond simple light emission are presented and possible future directions for light‐emitting transistors with added functionalities are outlined.     

Programmable polymer light emitting transistors with ferroelectric polarization-enhanced channel current and light emission

We present a voltage programmable polymer light emitting field-effect transistor (LEFET), consisting of a green emitting polymer (F8BT), and a ferroelectric polymer, P(VDF-TrFE), as the gate dielectric. We show by both experimental observations and numerical modeling that, when the ferroelectric gate dielectric is polarized in opposite directions at the drain and source sides of the channel, respectively, both electron and hole currents are enhanced, resulting in more charge recombination and ～10 times higher light emission in a ferroelectric LEFET, compared to the device with non-ferroelectric gate. As a result of the ferroelectric poling, our ferroelectric LEFETs exhibit repeated programmability in light emission, and an external quantum efficiency (EQE) of up to 1.06%. Numerical modeling reveals that the remnant polarization charge of the ferroelectric layer tends to ‘pin’ the position of the recombination zone, paving the way to integrate specific optical out-coupling structures in the channel of these devices to further increase the brightness.     

Stacked pentacene layer organic thin-film transistors with improvedcharacteristics

Using two layers of pentacene deposited at different substrate temperatures as the active material, we have fabricated photolithographically defined organic thin-film transistors (OTFTs) with improved field-effect mobility and subthreshold slope. These devices use photolithographically defined gold source and drain electrodes and octadecyltrichlorosilane-treated silicon dioxide gate dielectric. The devices have field-effect mobility as large as 1.5 cm²/V-s, on/off current ratio larger than 10⁸, near zero threshold voltage, and subthreshold slope less than 1.6 V per decade. To our knowledge, this is the largest field-effect mobility and smallest subthreshold slope yet reported for any organic transistor, and the first time both of these important characteristics have been obtained for a single device     

Micromolding in capillaries and microtransfer printing of silver nanoparticles as soft-lithographic approach for the fabrication of source/drain electrodes in organic field-effect transistors

Within the past years there has been much effort in developing and improving new techniques for the processing of advanced functional materials used in promising applications like micro-optics or organic electronics. Much attention has been paid to solution-based techniques, which enable low-cost processing and new possible developments like flexible displays or inkjet printed electronics. An alternative approach to inkjet printing is soft-lithography, which is a collective term for a number of non-photolithographic techniques and has become an important tool for the micron-sized structuring of materials.Here we report on the use of micromolding in capillaries (MIMIC) and microtransfer printing (μTP) as two soft-lithographic techniques for the fabrication of silver source/drain electrodes in well-performing bottom-gate/bottom-contact organic field-effect transistors (OFETs) with poly(3-hexylthiophene) as active layer material.While MIMIC combines solution-processability with high lateral resolution for highly accurate patterns, μTP is the miniaturized counterpart to conventional letterpress printing.The performance of the OFETs fabricated with these techniques is similar to devices based on conventional gold source/drain electrodes with well-defined source-to-drain current saturation and a linear behavior at low drain voltages suggesting a low contact resistance and hence good carrier injection from the silver electrodes into the organic semiconductor.     

Solution‐Processed Organic Light‐Emitting Transistors Incorporating Conjugated Polyelectrolytes

Improved performance of p‐type organic light‐emitting transistors (OLETs) is demonstrated by introducing a conjugated polyelectrolyte (CPE) layer and symmetric high work function (WF) source and drain metal electrodes. The OLET comprises a tri‐layer film consisting of a hole transporting layer, an emissive layer, and a CPE layer as an electron injection layer. The thickness of the CPE layer is critical for achieving good performance and provides an important structural handle for consideration in future optimization studies. We also demonstrate for the first time, good performance solution‐processed blue‐emitting OLETs. These results further demonstrate the simplification of device fabrication and improved performance afforded by integrating CPE interlayers into organic optoelectronic devices.     

Organische Feldeffekttransistoren auf Basis halbleitender Polymere

At present a variety of companies and institutes in the world are working on the development of organic field-effect transistors (OFET) and integrated polymer circuits (IPCs) to create a new low-cost low-performance electronics. This is especially suited for low-end electronics and RFID applications like electronic labels, smart cards, ident tags, electronic bar codes etc., which are needed in large amounts at lowest prices. The transistors are made as thin film transistors on flexible or rigid substrates by successive coating with the appropriate functional materials (polymer semiconductor, insulator, layers for electrodes). This setup can be realized either by organic and polymer materials only as well as by a combination of organic with inorganic materials. All-polymer field-effect transistors (PFETs) which completely consist of polymer layers (source, drain and gate electrodes, semiconductor, insulator) are of special interest. Later on they will offer the chance to use printing techniques for their production which enables high-volume printing of electronic circuits.     

Mapping charge carrier density in organic thin-film transistors by time-resolved photoluminescence lifetime studies

The device performance of organic transistors is strongly influenced by the charge carrier distribution. A range of factors effect this distribution, including injection barriers at the metal-semiconductor interface, the morphology of the organic film, and charge traps at the dielectric/organic interface or at grain boundaries. In our comprehensive experimental and analytical work we demonstrate a method to characterize the charge carrier density in organic thin-film transistors using time-resolved photoluminescence spectroscopy. We developed a numerical model that describes the electrical and optical responses consistently. We determined the densities of free and trapped holes at the interface between the organic layer and the SiO₂ gate dielectric by comparison to electrical measurements. Furthermore by applying fluorescence lifetime imaging microscopy we determine the local charge carrier distribution between source and drain electrodes of the transistor for different biasing conditions. We observe the expected hole density gradient from source to drain electrode.     

真空气相沉积生长PTCDI C8 N型有机薄膜晶体管

在大气环境下N型有机薄膜晶体管(OFET)的性能不稳定,为提高晶体管在大气环境稳定性,该文分别制作了SiO2单绝缘层器件和SiO2/PMMA双绝缘层器件。采用N型新材料PTCDI-C8作为有源层,Ag作为源、漏电极,对制作的不同绝缘层的器件进行聚对二甲苯的封装,对有源层进行形貌和晶体结构分析。并进行电流-电压(I-V)曲线测试。在相同工作电压下,双绝缘层器件比单绝缘层器件具有更大的场效应迁移率、开关电流比和更小的阈值电压。     

Simultaneous Tenfold Brightness Enhancement and Emitted‐Light Spectral Tunability in Transparent Ambipolar Organic Light‐Emitting Transistor by Integration of High‐k Photonic Crystal

In organic light‐emitting transistors, the structural properties such as the in‐plane geometry and the lateral charge injection are the key elements that enable the monolithic integration of multiple electronic, optoelectronic, and photonic functions within the same device. Here, the realization of highly integrated multifunctional optoelectronic organic device is reported by introducing a high‐capacitance photonic crystal as a gate dielectric into a transparent single‐layer ambipolar organic light‐emitting transistor (OLET). By engineering the photonic crystal multistack and bandgap, it is showed that the integration of the photonic structure has a twofold effect on the optoelectronic performance of the device, i.e., i) to modulate the spectral profile and outcoupling of the emitted light and ii) to enhance the transistor source–drain current by a 25‐fold factor. Consequently, the photonic‐crystal‐integrated OLET shows an order of magnitude higher emitted power and brightness with respect to the corresponding polymer‐dielectric device, while presenting as‐designed electroluminescence spectral and spatial distribution. The results validate the efficacy of the proposed approach that is expected to unravel the technological potential for the realization of highly integrated optoelectronic smart systems based on organic light‐emitting transistors.     

Bottom-contact poly(3,3‴-didodecylquaterthiophene) thin-film transistors with reduced contact resistance

A dramatic, ∼20-fold, reduction in the contact resistance of the bottom-contact poly(3,3‴-didodecylquaterthiophene) (PQT-12) thin-film transistors was achieved through a simple treatment of gold (Au) source and drain electrodes. The Au electrode treatment involved simply immersing the Au electrodes into Piranha solution prior to the deposition of the organic semiconductor. This treatment led to significant improvement of device performance. Channel length scaling analysis indicates that the contact resistance is reduced by about one order of magnitude, resulting in enhancement of estimated field-effect mobility by about a factor of five. Transport characteristic analysis suggests that the improved efficiency of charge carrier injection is probably due to increased dopant density of PQT-12 at the electrode/PQT-12 interface.     

Radical polymers improve the metal-semiconductor interface in organic field-effect transistors

Modifying the organic-metal interface in organic field-effect transistors (OFETs) is a critical means by which to improve device performance; however, to date, all of the interfacial modifying layers utilized in these systems have been closed-shell in nature. Here, we introduce open-shell oxidation-reduction-active (redox-active) macromolecules, namely radical polymers, in order to serve as interfacial modifiers in pentacene-based OFETs. Through careful selection of the chemistry of the specific radical polymer, poly(2,2,6,6-tetramethylpiperidine-1-oxyl methacrylate) (PTMA), the charge transport energy level of the interfacial modifying layer was tuned to provide facile charge injection and extraction between the pentacene active layer and the gold source and drain electrodes of the OFET. The inclusion of this radical polymer interlayer, which was deposited in through straightforward inkjet printing, led to bottom-contact, bottom-gate OFETs with significantly increased mobility and ON/OFF current ratios relative to OFETs without the PTMA interlayer. The underlying mechanism for this improvement in device performance is explained in terms of the charge transport capability at the organic-metal interface and with respect to the pentacene grain growth on the radical polymer. Thus, this effort presents a new, open-shell-based class of materials for interfacial modifying materials, and describes the underlying physics behind the practical operation of these materials.     

Inkjet‐Printed Organic Electrodes for Bottom‐Contact Organic Field‐Effect Transistors

A graphite thin film was investigated as the drain and source electrodes for bottom‐contact organic field‐effect transistors (BC OFETs). Highly conducting electrodes (10² S cm^?1) at room temperature were obtained from pyrolyzed poly(l,3,4‐oxadiazole) (PPOD) thin films that were prepatterned with a low‐cost inkjet printing method. Compared to the devices with traditional Au electrodes, the BC OFETs showed rather high performances when using these source/drain electrodes without any further modification. Being based on a graphite‐like material these electrodes possess excellent compatibility and proper energy matching with both p‐ and n‐type organic semiconductors, which results in an improved electrode/organic‐layer contact and homogeneous morphology of the organic semiconductors in the conducting channel, and finally a significant reduction of the contact resistance and enhancement of the charge‐carrier mobility of the devices is displayed. This work demonstrates that with the advantages of low‐cost, high‐performance, and printability, PPOD could serve as an excellent electrode material for BC OFETs.     

Air stability of n-channel organic transistors based on nickel coordination compounds

A series of tetraphenyl nickel dithiolene complexes, 1, are prepared, and the air stability of the n-channel organic field-effect transistors (OFET) is investigated. The fluoro and trifluoromethyl derivatives with reduction potentials higher than 0 V afford reasonably air-stable n-channel OFET. Metallic organic charge-transfer complex (TTF)(TCNQ) (TTF: tetrathiafulvalene and TCNQ: tetracyanoquinodimethane) is used as source and drain electrodes, and realizes n-channel transistor properties even when Al electrodes do not work.     

High-speed operation in printed organic inverter circuits with short channel length

We have demonstrated fast operation of printed organic inverter circuits. We employ a soluble organic semiconducting material which has high field-effect mobility and ink-jet printed source/drain electrodes with short channel length. Appropriate concentration of the semiconducting solution and modification layer of source/drain electrodes improve both mobility and on/off ratio. The fabricated transistors with a short channel length (4 μm) exhibit excellent mobility (1.2 cm²/V s), high on/off ratio (>10⁵) and operational stability. The diode-load inverter with a narrow channel and low parasitic capacitance operate at 8 kHz at 20 V. These results will lead to significant progress in applications of printed organic circuits.