Designing π-conjugated polymers for organic electronics

Conjugated polymers have attracted an increasing amount of attention in recent years for various organic electronic devices because of their potential advantages over inorganic and small-molecule organic semiconductors. Chemists can design and synthesize a variety of conjugated polymers with different architectures and functional moieties to meet the requirements of these organic devices. This review concentrates on five conjugated polymer systems with 1D and 2D topological structures, and on one polymer designing approach. This includes (i) conjugated polyphenylenes (polyfluorenes, polycarbazoles, and various stepladder polymers), (ii) other polycyclic aromatic hydrocarbons (PAHs) as substructures of conjugated polymers, (iii) thiophene and fused thiophene containing conjugated polymers, (iv) conjugated macrocycles, (v) graphene nanoribbons, and finally (vi) a design approach, the alternating donor–acceptor (D–A) copolymers. By summarizing the performances of the different classes of conjugated polymers in devices such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and polymer solar cells (PSCs), the correlation of polymer structure and device property, as well as the remaining challenges, will be highlighted for each class separately. Finally, we summarize the current progress for conjugated polymers and propose future research opportunities to improve their performance in this exciting research field.     

白色有机电致发光材料与器件

综述白色有机电致发光材料和器件的研究进展。归纳了获取白色有机电致发光的途径和方法。分析了多种器件结构的特点及其材料。结合研究过程中存在的某些问题,从器件的发光效率和色纯度角度,讨论了影响发光器件性能的诸因素及其改进措施。     

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.     

Recent advances in conjugated polymers for light emitting devices

A recent advance in the field of light emitting polymers has been the discovery of electroluminescent conjugated polymers, that is, kind of fluorescent polymers that emit light when excited by the flow of an electric current. These new generation fluorescent materials may now challenge the domination by inorganic semiconductor materials of the commercial market in light-emitting devices such as light-emitting diodes (LED) and polymer laser devices. This review provides information on unique properties of conjugated polymers and how they have been optimized to generate these properties. The review is organized in three sections focusing on the major advances in light emitting materials, recent literature survey and understanding the desirable properties as well as modern solid state lighting and displays. Recently, developed conjugated polymers are also functioning as roll-up displays for computers and mobile phones, flexible solar panels for power portable equipment as well as organic light emitting diodes in displays, in which television screens, luminous traffic, information signs, and light-emitting wallpaper in homes are also expected to broaden the use of conjugated polymers as light emitting polymers. The purpose of this review paper is to examine conjugated polymers in light emitting diodes (LEDs) in addition to organic solid state laser. Furthermore, since conjugated polymers have been approved as light-emitting organic materials similar to inorganic semiconductors, it is clear to motivate these organic light-emitting devices (OLEDs) and organic lasers for modern lighting in terms of energy saving ability. In addition, future aspects of conjugated polymers in LEDs were also highlighted in this review.     

抗冻水凝胶的制备及其在柔性电子领域的应用

水凝胶具有优异的柔韧性、离子运输性和可调的机械性,在柔性电子领域具有广阔的应用前景,然而,水凝胶电子器件在严寒气候下容易冻结失效,严重限制了其在低温环境下的应用潜力,通过向水凝胶中引入低温防护剂可以赋予水凝胶抗冻性能,拓宽水凝胶电子器件的工作温度。该文从溶质离子、离子液体、有机溶剂以及抗冻蛋白改性水凝胶4个方面,综述了近年来抗冻水凝胶的制备方法和抗冻机理,阐述了抗冻水凝胶在超级电容器、传感器和电池等柔性电子领域的应用进展,归纳了抗冻水凝胶电子材料面临的问题与挑战,并展望了抗冻水凝胶电子材料的发展趋势,指出以天然可再生资源为原料开发具有优异机械性能、电化学性能、生物无毒性、生物相容性和生物可降解的抗冻水凝胶成为下一步研究重点,同时设计优化柔性电子装置、提高器件安全可靠性和输出稳定性也将成为重要的研究方向之一。抗冻水凝胶的制备及其应用研究将促进柔性电子功能材料领域的快速发展。     

Recent Advances in Solution-Processed White Organic Light-Emitting Materials and Devices

Solution-processed white organic light-emitting diodes (WOLEDs) have drawn great attention both in the academic and industrial research communities due to the potential application in low-cost, large-area, solid-state lightings. Issues related to the device efficiencies are largely hampering progress in this field. Alongside the development of new materials and novel device architectures, distinct progress has been made for such white devices. In particular, the all-phosphorescent light-emitting strategy has been intensively developed in recent years, mainly focusing on a host guest, doping-system-based, single-active-layer structure and a solution-processed, multilayer device structure. Novel approaches, including white single polymers and excimer-/exciplex-based white devices, have also appeared as a promising choice and received great attention. As a prerequisite, the issue of the morphology of the emissive layer is also important and has an influence on the optoelectronic behavior of the device. Herein, major advances in solution-processed WOLEDs based on polymers, dendrimers, or solution-processed small molecules are summarized. Special attention is focused on the main progress in high-efficiency, solution-processed WOLEDs with the key strategies mentioned above and the morphology issue in these systems. The remaining challenges in pursuing the development of reliable and energy-saving lighting devices are also discussed.     

Adhesive lithography for fabricating organic electronic and optoelectronics devices

Improvements in organic electronic materials have led to novel device applications, ranging from large-area flexible displays to lightweight plastic electronics. Progress on these applications would benefit from development of low-cost fabrication techniques for organic semiconductors. In this review, several fabrication processes based on adhesion force (i.e. van der Waals forces, thiol-metal reactions, and cold welding) are introduced. These patterning techniques are dry patterning techniques, i.e., the electronic materials are patterned from the raised regions of molds onto a substrate directly by additive or subtractive patterning methods. Patterning of organic small molecule, polymer thin films and metal electrodes by adhesive lithography is demonstrated. The operating properties of patterned organic light-emitting diodes (OLEDs) and organic thin film transistors (OTFTs) are comparable with the performance of devices fabricated by conventional evaporation deposition methods.     

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.     

有机电致发光材料研究新进展

简要介绍了有机电致发光器件的结构、工作原理。重点从有机电致发光材料器件结构的角度出发,对电致发光材料最新研究进展进行了综述。     

Conjugated-polymer grafting on inorganic and organic substrates: A new trend in organic electronic materials

This review highlights recent developments in the grafting of conjugated polymers onto various substrates for organic electronic devices. The rapid development of multi-layer architectures demands the preparation of well-defined interfaces between both compatible and incompatible materials. It is promising therefore that interface-engineering is now known to help passivate charge trap states, control energy level alignments, enhance charge extraction, guide active-layer morphologies, and improve material compatibility, adhesion and device stability. In organic electronic devices, conjugated polymers are in contact with a wide range of constituents, such as metals, metal oxides, organic materials, and inorganic particles. Covalent bonds between these materials and macromolecules are desired to yield intimate contacts and well-defined interfaces. Following an overview of the various synthetic methodologies of conjugated polymers, the chemistry of tethering macromolecular chains onto nanoparticles and flat surfaces is described. The creation of functional hybrid materials offers the potential to deliver efficient and low-cost devices.     

Encapsulation of organic light-emitting devices by means of photopolymerized polyacrylate films

For encapsulation of organic light-emitting devices (OLEDs) built on glass substrate, photopolymerizable blend consists of pentaerythritol triacrylate (PETIA) and HSP188 (photoinitiator) was spin-coated onto an OLED and then cured to form a cross-linked passivation layer. The electroluminescence (EL) and the rate of degradation were examined to compare the electrical and the emissive properties of the device before and after forming the passivation layer. In this case, wet process encapsulation, which did not influence the EL characteristic of the device, enhanced the lifetime of the device in air.     

Piezoresistive effect in spin-coated polyaniline thin films

Polymeric materials have been replacing other materials in various applications, from structural to electronic components. In particular, since the discovery of conducting polymers, the use of these materials is growing up in the manufacture of electronic components, such as organic light-emitting diodes, organic electrodes, energy storage devices and artificial muscles, among others. On the other hand, examples of sensors of conductive polymers based on the piezoresistive effect, with large potential for applications, are not sufficiently investigated. This work reports on the piezoresistive effect of an intrinsically conductive polymer, polyaniline, which was prepared in the form of thin films by spin coating on polyethylene terephthalate substrates. The relationship between electrical response and mechanical solicitations is presented for different preparation conditions. The values of the gauge factor ranges from 10 to 22 for different samples and demonstrates the viability of these materials as piezoresistive sensors.     

Conjugated polyelectrolytes: A new class of semiconducting material for organic electronic devices

This feature article presents a short review of the recent developments in the synthesis of conjugated polyelectrolytes (CPEs) along with their applications in organic optoelectronic devices with particular focus on the molecular structures of CPEs with ionic functionality, synthetic approaches, and their utilization as an interfacial layer. The orthogonal solubility of the CPEs allows the simple preparation of multilayer organic devices by solution casting on top of a nonpolar organic photoactive layer without disturbing the interfaces, showing their effectiveness in tuning the electronic structures at the interfaces for improving the charge carrier transport and resulting device properties. These achievements highlight the dynamic nature of CPEs and their applicability to a wide range of optoelectronic devices.     

倍半硅氧烷基电致发光材料的研究进展

有机电致发光器件(OLED)作为一种新型显示器件,其结构简单、易于制造、成本更低、性能更好,未来在各领域将有很大的应用潜力。其中电致发光材料是OLED的核心材料,是OLED能否工业化生产的关键因素,但目前发光材料仍存在一些不足。多面体倍半硅氧烷(POSS)作为一种笼状无机材料,由于具有良好的耐热性、力学强度、稀释效应,经常与咔唑、芴等有机物杂化,从而有效地改善光电和物理性能,被用作OLED电致发光材料,已得到当前电致发光研发领域的极大关注。本文主要介绍了倍半硅氧烷基电致发光材料的研究进展。     

Phosphonate-functionalized polyfluorene and its application in organic optoelectronic devices

Conjugated polar polymers, in which the conjugated backbones are chemically anchored with functional polar side groups, can be processed with water/alcohol solvents, and thus multilayered device architectures can be easily realized via sequential solution processing of the toluene-soluble emissive polymer and alcohol-soluble electron-transporting polymer without intermixing. Regarding their use in organic optoelectronic devices, the success in achieving efficient charge injection and intimate contact between metal electrodes and organic semiconductors is very vital for enhancing the device performance. In this short review, it gives a brief review to neutral alcohol-soluble phosphonate-functionalized polyfluorene, mainly concerning the electronic structure at the phosphonate-functionalized polyfluorene/aluminum cathode interface and its successful application in multilayered polymer optoelectronic devices including polymer light-emitting diodes and polymer solar cells.     

Modern Drifts in Conjugated Polymers and Nanocomposites for Organic Solar Cells: A Review

In this article, various aspects of photovoltaic, organic solar cell and working principle involved have been reviewed. Moreover, different generations of solar cell, and use of an important class of organic materials, i.e., conjugated polymers and polymer-based nanocomposites and their properties were discussed. Convincingly, organic materials have vast future potential in solar cell to enhance its efficiency and durability of devices. In the review, current understandings of mechanisms that rule the photocurrent creation steps and define seek for alternate materials and device structure, have been focused. Foremost research efforts must focus cell efficiency improvement to speed up new material commercialization.     

Protein Nanofibrils Balance Colours in Organic White-Light-Emitting Diodes

In this review we discuss our efforts in using protein nanowires (amyloid fibrils) as structural templates for use in organic electronics applications, mainly focusing on organic light-emitting diodes (OLEDs). We discuss different ways of functionalising amyloid fibrils. In one method, the amyloid fibril is used to organise luminescent polymers. We also discuss an alternative preparative method, resulting in amyloid-like materials functionalised with phosphorescent organometallic complexes. We discuss the incorporation of such materials in organic electronics devices, such as OLEDs. When amyloid fibrils are integrated into the OLED active layer, consisting of an electroluminescent blue-emitting polyfluorene, the efficiency of the device increases by a factor of 10. Furthermore, when amyloid fibrils incorporating phosphorescent metal complexes are used, the phosphorescent guest functions more efficiently than in the corresponding case where naked metal complexes are used. By preparing amyloid fibrils incorporating green- and red-emitting phosphorescent complexes, and combining these with blue-emitting polyfluorene, we can fabricate devices for white-light emission. The origin of the effects of the biomaterial on device performance is discussed.     

Electrochemical synthesis of poly(3′-alkyl-terthiophenes). Characterization and applications

A new series of polymers obtained from 3′-alkyl-terthiophene monomers have been electropolymerized aimed at using them as raw materials for the development of electronic devices, e.g., solar cell and organic light-emitting diodes, among others. The polymers were characterized by infrared and UV–Vis spectroscopy and cyclic voltammetry. Cyclic voltammetry results revealed that during polymerization both terthiophene system and substituent groups are oxidized, but these processes are reversible. The products were tested in solar cells and the maximum yield obtained was 0.01%.     

Polyfluorene-based semiconductors combined with various periodic table elements for organic electronics

Polyfluorenes have emerged as versatile semiconducting materials with applications in various polymer optoelectronic devices, such as light-emitting devices, lasers, solar cells, memories, field-effect transistors and sensors. Organic syntheses and polymerizations allow for the powerful introduction of various periodic table elements and their building blocks into π-conjugated polymers to meet the requirements of organic devices. In this review, a soccer-team-like framework with 11 nodes is initially proposed to illustrate the structure-property relationships at three levels: chain structures, thin films and devices. Second, the modelling of hydrocarbon polyfluorenes (CPFs) is summarized within the framework of a four-element design principle, in which we have highlighted polymorphic poly(9,9-dialkylfluorene)s with unique supramolecular interactions, various hydrocarbon-based monomers with different electronic structures, functional bulky groups with steric hindrance effects and ladder-type, kinked, hyperbranched and dendritic conformations. Finally, the detailed electronic structure designs of main-chain-type heteroatomic copolyfluorenes (HPFs) and metallopolyfluorenes (MPFs) are described in the third and fourth sections. Supramolecular, nano and soft semiconductors are the future of polyfluorenes in the fields of optoelectronics, spintronics and electromechanics.     

Synthesis and electroluminescence property of new hexaphenylbenzene derivatives including amine group for blue emitters

Three new blue-emitting compounds of 5P-VA, 5P-VTPA, and 5P-DVTPA for organic light-emitting diode (OLED) based on hexaphenylbenzene moiety were demonstrated. Physical properties by the change of the substitution groups of the synthesized materials were systematically examined. Photoluminescence spectrum of the synthesized materials showed maximum emitting wavelengths of about 400 to 447 nm in solution state and 451 to 461 nm in film state, indicating deep blue emission color. OLED devices were fabricated by the synthesized compounds using vacuum deposit process as an emitting layer. The device structure was ITO/2-TNATA 60 nm/ NPB 15 nm/ EML 35 nm/ TPBi 20 nm/ LiF 1 nm/ Al 200 nm. External quantum efficiencies and CIE values of 5P-VA, 5P-VTPA, and 5P-DVTPA were 1.89%, 3.59%, 3.34%, and (0.154, 0.196), (0.150, 0.076), (0.148, 0.120), respectively. 5P-VTPA and 5P-DVTPA exhibited superior highly blue quality and thermal property such as high T_d of 448°C and 449°C.