Biomaterials‐based organic electronic devices

Organic electronic devices have demonstrated tremendous versatility in a wide range of applications including consumer electronics, photovoltaics and biotechnology. The traditional interface of organic electronics with biology, biotechnology and medicine occurs in the general field of sensing biological phenomena. For example, the fabrication of hybrid electronic structures using both organic semiconductors and bioactive molecules has led to enhancements in the sensitivity and specificity within biosensing platforms, which in turn has a potentially wide range of clinical applications. However, the interface of biomolecules and organic semiconductors has also recently explored the potential use of natural and synthetic biomaterials as structural components of electronic devices. The fabrication of electronically active systems using biomaterials‐based components has the potential to produce a large set of unique devices including environmentally biodegradable systems and bioresorbable temporary medical devices. This article reviews recent advances in the implementation of biomaterials as structural components in organic electronic devices with a focus on potential applications in biotechnology and medicine. Copyright © 2010 Society of Chemical Industry     

n-Channel semiconductor materials design for organic complementary circuits

Organic semiconductors have unique properties compared to traditional inorganic materials such as amorphous or crystalline silicon. Some important advantages include their adaptability to low-temperature processing on flexible substrates, low cost, amenability to high-speed fabrication, and tunable electronic properties. These features are essential for a variety of next-generation electronic products, including low-power flexible displays, inexpensive radio frequency identification (RFID) tags, and printable sensors, among many other applications. Accordingly, the preparation of new materials based on π-conjugated organic molecules or polymers has been a central scientific and technological research focus over the past decade. Currently, p-channel (hole-transporting) materials are the leading class of organic semiconductors. In contrast, high-performance n-channel (electron-transporting) semiconductors are relatively rare, but they are of great significance for the development of plastic electronic devices such as organic field-effect transistors (OFETs). In this Account, we highlight the advances our team has made toward realizing moderately and highly electron-deficient n-channel oligomers and polymers based on oligothiophene, arylenediimide, and (bis)indenofluorene skeletons. We have synthesized and characterized a "library" of structurally related semiconductors, and we have investigated detailed structure-property relationships through optical, electrochemical, thermal, microstructural (both single-crystal and thin-film), and electrical measurements. Our results reveal highly informative correlations between structural parameters at various length scales and charge transport properties. We first discuss oligothiophenes functionalized with perfluoroalkyl and perfluoroarene substituents, which represent the initial examples of high-performance n-channel semiconductors developed in this project. The OFET characteristics of these compounds are presented with an emphasis on structure-property relationships. We then examine the synthesis and properties of carbonyl-functionalized oligomers, which constitute second-generation n-channel oligothiophenes, in both vacuum- and solution-processed FETs. These materials have high carrier mobilities and good air stability. In parallel, exceptionally electron-deficient cyano-functionalized arylenediimide derivatives are discussed as early examples of thermodynamically air-stable, high-performance n-channel semiconductors; they exhibit record electron mobilities of up to 0.64 cm(2)/V·s. Furthermore, we provide an overview of highly soluble ladder-type macromolecular semiconductors as OFET components, which combine ambient stability with solution processibility. A high electron mobility of 0.16 cm(2)/V·s is obtained under ambient conditions for solution-processed films. Finally, examples of polymeric n-channel semiconductors with electron mobilities as high as 0.85 cm(2)/V·s are discussed; these constitute an important advance toward fully printed polymeric electronic circuitry. Density functional theory (DFT) computations reveal important trends in molecular physicochemical and semiconducting properties, which, when combined with experimental data, shed new light on molecular charge transport characteristics. Our data provide the basis for a fundamental understanding of charge transport in high-performance n-channel organic semiconductors. Moreover, our results provide a road map for developing functional, complementary organic circuitry, which requires combining p- and n-channel transistors.     

Polyurethane adhesives for electronic devices

The choice of polymeric materials in electronic packaging influences not only the performance parameters of electronic devices, but also their long-term reliability. Adverse conditions such as humidity, high temperature, and vibration prevent the electronic devices from functioning in the way that they were designed. This paper presents the results of experimental work aimed at studying the properties of new room temperature-setting polydiene urethane adhesives (PUAs). Based on hydroxyl-containing oligodiene urethanes, new PUAs were investigated for their mechanical and dielectric properties. It was found that the adhesives were highly elastic, stable against temperature and humidity, and had good dielectric characteristics. Reliability tests on printed circuit boards with the bonded electronic components were carried out in various conditions. The electrical resistance changes of bonded resistors were found to be in the range of 0.03-1.4% after all tests. It can be concluded that these adhesives do not adversely affect the performance of electronic components and can be used for the assembling of electronic devices in addition to conventional soldering.     

Effect of UV/ozone treatment on polystyrene dielectric and its application on organic field-effect transistors

The influence of UV/ozone treatment on the property of polystyrene (PS) dielectric surface was investigated, and pentacene organic field-effect transistors (OFETs) based on the treated dielectric was fabricated. The dielectric and pentacene active layers were characterized by atomic force microscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy. The results showed that, at short UVO exposure time (<10 s), the chemical composition of PS dielectric surface remained the same. While at long UVO exposure time (>60 s), new chemical groups, including alcohol/ether, carbonyl, and carboxyl/ester groups, were formed. By adjusting the UVO exposure time to 5 s, the hole mobility of the OFETs increased to 0.52 cm²/Vs, and the threshold voltage was positively shifted to -12 V. While the time of UVO treatment exceeded 30 s, the mobility started to shrink, and the off-current was enlarged. These results indicate that, as a simple surface treatment method, UVO treatment could quantitatively modulate the property of PS dielectric surface by controlling the exposure time, and thus, pioneered a new way to modulate the characteristics of organic electronic devices.     

Organic materials for organic electronic devices

In recent years, organic electronic devices which use organic materials as an active layer have gained considerable interest as light-emitting devices, energy converting devices and switching devices in many applications. In these organic electronic devices, the organic materials play a key role of managing the device performances and various organic materials have been developed to improve the device performances of organic electronic devices. In this paper, recent developments of organic electronic materials for organic light-emitting diodes and organic solar cells were reviewed.     

$$\pi$$-Conjugated Heterocyclic fused Bithiophene Materials

This article covers the developments on the synthesis and properties of heterocyclic fused π-conjugated bithiophene materials that are potentially applicable in molecular electronics and optoelectronics. This fairly young strategy to efficiently tuning the electronic properties generates materials with very narrow band gaps. The nature of the central bridging heteroatom has a significant impact on the electronic and luminescence properties of these materials leading to intriguing species that can be employed in organic light emitting diodes (OLEDs) or organic field effect transistors (OFETs). So far a variety of heteroelements of group 13–16 (B, Si, Ge, Sn, N, P, S) have been investigated and incorporated into molecular as well as polymeric systems. A significant number of these materials can potentially act as organic emitters, electron or hole transport materials in organic devices but further studies are needed to optimize the necessary properties for the utility of this young class of compound in molecular electronics.     

One-dimensional electrospun ceramic nanomaterials and their sensing applications

One-dimensional sensing materials that are prepared via electrospinning and controlled annealing exhibit intrinsic properties, such as electron transmissivity, magnetic susceptibility, specific heat capacity, as well as optical and mechanical characteristics. Particularly, the electronic transmission characteristics of the ceramic fiber materials, such as the electrical conductivity, photocurrent, magnetoresistance, nanocontact resistance, and dielectric properties, exhibited great potential for applications in the next generation of electronic sensing devices. First, electrospun ceramic materials with different structural and functional characteristics were reviewed here, after which the strategies for improving their properties, as well as the method for assembling the flexible devices, are summarized. Moreover, the electrospun ceramic nanofibers were detailedly discussed regarding applications in device construction and wearable electronics, such as photosensors, gas sensors, mechanical sensors, and other energy storage devices. Finally, the future development direction of the electrospinning technology for multifunctional and wearable electronics skin was proposed.     

High‐Performance Flexible Pressure and Temperature Sensors with Complex Leather Structure

The ability of the skin to be pressure‐sensitive has prompted scientists to develop materials and equipment to simulate this function. Recently, flexible and stretchable artificial electronic skin has received increasing attention with its unique ability to detect subtle pressure changes. Pressure sensing is one of the key functions of electronic skin devices. Here, a stretchy and highly sensitive pressure sensor is developed that used a polydimethylsiloxane (PDMS) film with leather composite layer as flexible part. These features enable the sensor to accurately detect a variety of human activities, such as small finger movements and bending, pulse and so on. The sensor is found to have a good sensing signal for temperature. This feature provides great promise for sensors to detect temperature.     

Stretchable and self-healing polymers and devices for electronic skin

This review covers some of the most recent advances in stretchable and self-healing polymers and devices for Electronic skin (E-skin) applications. Applications for both stretchable and self-healing materials include, but are not limited to, electronics, displays, energy, the environment, and medicine. While the majority of organic materials can generally be rendered flexible, such materials are not stretchable, which is a key mechanical property necessary to realize applications of E-skin for prosthetics, artificial intelligence, systems for robotics, personal health monitoring, biocompatibility, and communication devices. In our effort to survey materials utilized in various components of an electronic device, we report herein recent advances in stretchable and self-healing conductors, semiconductors, and substrates. We highlight some key technologies recently developed in stretchable organic-based sensors, solar cells, light-emitting diodes, and self-healing electronic devices.     

Construction of fluorenyl-modified low dielectric constant polyimide films with excellent mechanical properties and optical transparency

In order to meet the requirements of highly integrated and miniaturized electronic components, there is an urgent need for low dielectric materials with high mechanical properties and optical transparency in the field of microelectronics. In this study, a series of novel polyimide films (FPI) containing fluorenyl were prepared, and the effects of the fluorenyl content on the thermal, mechanical, and dielectric properties of the copolymerized films were investigated and discussed. The results demonstrate a significant decrease in the dielectric constant of the FPI films following the introduction of fluorenyl into polyimide (PI) chain segment. The FPI films also exhibited high mechanical properties, including tensile strengths between 92 and 106 MPa and elongation at break in the range of 8.4%–13.0%. Additionally, the introduction of the noncoplanar fluorenyl considerably improved the optical transparency and solubility of the FPI film. It is noteworthy that the FPI-3 has the best dielectric properties, with a low dielectric constant of 2.61 at 10 MHz and shows low water absorption (0.49%). The results show that we have prepared a novel low dielectric PI material film with excellent mechanical properties and optical transparency by introducing fluorenyl into the PI chain segment. These FPI films with satisfactory properties may be good candidates for dielectric materials for electronic components.     

Effect of glassy carbon addition and photodegradation on the biodegradation in aqueous medium of poly (3-hydroxybutyrate-co-3-hydroxyvalerate)/glassy carbon green composites

The use of biodegradable polymers is an interesting way to reduce the polymeric waste accumulation in the environment. However, the addition of fillers to biodegradable polymer matrices may decrease their biodegradability. Glassy carbon (GC) is a promising carbon material that can be employed as a filler in the production of antistatic packaging utilized to protect electronic components. The use of a biodegradable polymeric matrix such as poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) can be an excellent alternative for the preparation of green composites to be used in these packages. This work aims to evaluate the effect of the GC addition and the GC particle size on the biodegradability of the PHBV matrix, as well as to study the result of the employment of a previous photodegradation treatment on the biodegradation in aqueous medium of PHBV/GC composites. Scanning electron microscopy, residual weight measurement (%) and surface roughness showed that GC does not interfere negatively with PHBV biodegradability. Differential scanning calorimetry analysis and residual weight measurement permitted to suggest that the increase in the crystallinity degree of PHBV and PHBV/GC samples occasioned by the ultraviolet radiation hindered the water and enzyme access to the bulk of the materials, decreasing the biodegradability.     

微波介质陶瓷低温共烧研究现状

微波介质陶瓷具有低介电常数、高品质因数和近零谐振频率温度系数的特点,满足微波器件向小型化、低成本化、集成化、和多功能化方向发展的特点。而微波介质陶瓷低温共烧又是满足微波介质电子元器件不断向小型化,轻量化,高集成度和高性能方向发展重要途径。本文对微波介质陶瓷实现低温共烧的途径进行了介绍,主要介绍了四种实现微波介质陶瓷低温共烧的方法。     

Increasing the performance of dielectric elastomer actuators: A review from the materials perspective

Electro-active polymers (EAPs) are emerging as feasible materials to mimic muscle-like actuation. Among EAPs, dielectric elastomer (DE) devices are soft or flexible capacitors, composed of a thin elastomeric membrane sandwiched between two compliant electrodes, that are able to transduce electrical to mechanical energy, actuators, and vice versa, generators. Initial studies concentrated mainly on dielectric elastomer actuators (DEAs) and identified the electro-mechanical principles and material requirements for an optimal performance. Those requirements include the need for polymers with high dielectric permittivity and stretchability and low dielectric loss and viscoelastic damping. Hence, attaining elastomeric materials with those features is the focus of current research developments. This review provides a systematic overview of such research, highlighting the advances, challenges and future applications of DEAs.     

Non-linear dielectric properties in based-PMN relaxor ferroelectrics

The investigation of the non-linear dielectric response in ferroelectric materials has become one of the most important issues in the field of ferroelectricity due to its technological and scientific interest. Rather, from the practical point of view the understanding of the non-linear dielectric properties is essential to improve the performance of ferroelectric multilayer capacitors and actuators devices, which commonly operate at high field levels. On the other hand, the non-linear (NL) dielectric response to large electric fields has been revealed as a powerful technique to investigate the physical origin of the dielectric relaxor state. In this work, low frequency dielectric measurements were performed in 0.9[Pb(Mg_1/3Nb_3/2)O₃]–0.1PbTiO₃ (PMN–PT) relaxor ceramics in a wide frequency and temperature range. The non-linear dielectric properties were investigated by using the measurements of the dielectric permittivity of the PMN–PT as a function of the dc “bias” driving field. The obtained results were analyzed within the framework of the current models for the dielectric response of relaxor ferroelectrics.     

Flexible dielectric ZnO-doped reduced graphene oxide bionanocomposites from solution blending for potential application in bio-related devices

Biocompatible materials with high dielectric constant and low dielectric loss have applications in bio-related electronic devices. Development of flexible materials with those properties is still a challenge. In this work, electrospun membranes and films are prepared from poly(vinyl alcohol) (PVA) and chitosan (CS) solutions, incorporated with a reduced graphene oxide-zinc oxide composite (rGO-ZnO). Blending CS with flexible PVA favors electrospinnability and mechanical properties. ZnO contributes to hinder agglomeration of conductive rGO sheets. The structural, mechanical, dielectric and electrical properties of the hybrid materials are investigated. Infrared spectroscopy reveals interaction between the filler and the polymeric components. For mats and films, the increase in rGO-ZnO content leads to lower crystallinity. The Young's modulus and stress at break values increase with increasing rGO-ZnO content. High dielectric constants (ε' = 132 to ε' = 166, at 10³ Hz), associated with low dielectric loss factor (tan δ = 0.02), are determined for the PVA/CS/rGO-ZnO films.     

Linear dielectric thermodynamics: A new universal law for optical,dielectric constants

The thermodynamics of linear dielectric are formally developed to explore the isothermal and adiabatic temperature-pressure dependence of dielectric constants. The refractive index of optical materials is widely measured in the literature: it is both temperature and pressure dependent. The argument to establish the dielectric constant's isentropic temperature dependence is a thermodynamic one and is thus applicable to all physical models that describe electron clouds and electronic resonances within materials. The isentropic slope of the displacement field vs the electric field at all temperatures is described by an adiabatic dielectric constant in an energy-per-unit mass system. This slope is shown through the electronic part of the entropy to be unstable at high temperatures due to the change in the curvature of the temperature dependence of the dielectric constant. The electronic entropy contribution for optical, thermo-electro materials has negative heat capacities which are unacceptable. The dielectric constant's temperature and pressure dependence is predicted to be only dependent on the specific volume so isentropes are always positive. A new universal form for the dielectric constant follows from this hypothesis: the dielectric constant is proportional to the square root of the specific volume for fully dense solids.     

Electrochemical Detection of Copper Using a Gly-Gly-His Modified Carbon Nanotube Biosensor

Diazonium ion chemistry has been used to electrochemically graft aminophenyl layers onto p-type silicon (100) substrates. A condensation reaction was used to immobilise single-walled carbon nanotubes with high carboxylic acid functionality directly to this layer. The surface immobilised carbon nanotubes were then modified with the tripeptide Gly-Gly-His for the selective detection of copper ions in aqueous environments. The stepwise assembly and sensitivity of this biosensor to copper was characterised by X-ray photoelectron spectroscopy and differential pulse voltammetry, respectively. The ability to detect copper ion concentrations down to 1 μM was demonstrated. As this biosensor combines the advantages of a silicon substrate for easy integration into sophisticated electrical and electronic devices, diazonium salt derived films for stability in aqueous environments and carbon nanotubes for desirable electrochemical properties, it is expected to have important future applications in environmental sensing.     

Organic thin film transistors: Materials,processes and devices

For the past ten years, organic materials have been extensively investigated as an electronic material for thin film transistor (TFT) devices. Organic materials offer strong promise in terms of properties, processing and cost effectiveness and they can be used in flat panel displays, imagers, smart cards, inventory tags and large area electronic applications. In this review, we summarize the current status of the organic thin film transistors including substrate materials, electrodes, semiconducting and dielectric layers; organic thin film preparation methods; morphological studies for organic thin films; electrical characterization of gate dielectric layers and semiconducting active layers; and characterization of the OTFTs. Future prospects and investigations required to improve the OTFT performance are also given. This paper is dedicated to Professor Hyun-Ku Rhee on the occasion of his retirement from Seoul National University.     

High-k composites with sandwich structure by introducing a negative permittivity layer with Ni as conductive filler

Advanced electronic equipment requires new high dielectric constant materials. Nevertheless, the balance of the permittivity and dielectric loss remained a problem. In this work, BFT/PVDF-Ni/PVDF sandwich polymer matrix composites (SPMCs) containing alternating negative dielectric constant and positive dielectric constant layers were fabricated using hot press sintering. The structure and dielectric properties of the composites were investigated. The results indicated that introducing negative dielectric constant layer into SPMCs led to higher dielectric constant (ε′ ≈ 130) and low loss tangent (tanδ ≈ 0.14) at 1 kHz compared with the pristine PVDF (ε′ ≈ 10, tanδ ≈ 0.020). The effective increase of dielectric constant was due primarily to the introduction of a negative dielectric layer into the material. The low loss tangent was caused by the ohm barrier effect between adjacent layers.     

Elevated temperature impact on performance of Low Temperature Co-fired Ceramic dielectrics

The need for electronics to operate at temperatures of 200°C and above continues to grow. These applications include avionics, aerospace, automotive, downhole drilling, mining, and many others. To satisfy this demand, a significant amount of research and development has been conducted. Despite the efforts, the number of new electronic components designed specifically for high-temperature operation is still relatively limited. In Low Temperature Co-fired Ceramic (LTCC) packages, LTCC materials are generally used as the host media for a number of pre-fabricated semiconductor components. As a result, reliability of the entire LTCC package largely depends on the performance of the least robust component. Ferro A6M-E and Ferro L8 are the two well-established and recognized LTCC dielectrics widely used for mid and high frequency LTCC applications, including several high reliability aerospace and defense applications that require demanding Mil-Spec qualifications. This study is our first attempt to characterize and understand basic high-temperature dielectric properties of these two commercial LTCC materials. The secondary objective is to initiate a dialogue in attempt to establish reliability requirements for LTCC packages dedicated for high-temperature operation.