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This review highlights the potential of Kelvin probe force microscopy (KPFM) beyond imaging to simultaneously study structural and electronic properties of functional surfaces and interfaces. This is of paramount importance since it is well established that a solid surface possesses different properties than the bulk material. The versatility of the technique allows one to carry out investigations in a non‐invasive way for different environmental conditions and sample types with resolutions of a few nanometers and some millivolts. KPFM can be used to acquire a wide knowledge of the overall electronic and electrical behavior of a sample surface. Moreover, by KPFM it is possible to study complex electronic phenomena in supramolecular engineered systems and devices. The combination of such a methodology with external stimuli, e.g., light irradiation, opens new doors to the exploration of processes occurring in nature or in artificial complex architectures. Therefore, KPFM is an extremely powerful technique that permits the unraveling of electronic (dynamic) properties of materials, enabling the optimization of the design and performance of new devices based on organic‐semiconductor nanoarchitectures.  相似文献   

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The patterning of functional materials represents a crucial step for the implementation of organic semiconducting materials into functional devices. Classical patterning techniques such as photolithography or shadow masking exhibit certain limitations in terms of choice of materials, processing techniques and feasibility for large area fabrication. The use of self‐assembled monolayers (SAMs) as a patterning tool offers a wide variety of opportunities, from the region‐selective deposition of active components to guiding the crystallization direction. Here, we discuss general techniques and mechanisms for SAM‐based patterning and show that all necessary components for organic electronic devices, i.e., conducting materials, dielectrics, organic semiconductors, and further functional layers can be patterned with the use of self‐assembled monolayers. The advantages and limitations, and potential further applications of patterning approaches based on self‐assembled monolayers are critically discussed.  相似文献   

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The dipyridamole drug [DIP: 2,6-bis(diethanolamino)-4,8-dipiperidinopyrimido(5,4-d)pyrimidine] is widely used in treatment of coronary heart disease for its antiplatelet and vasodilating activities, and its high intensity photoluminescence (PL) has been widely reported. In this work, the fabrication and the characterization of a new OLED using the DIP molecule as an emitting layer is reported. The devices were assembled using a heterojunction between three organic molecular materials: the N,N′-bis(naphthalen-1-yl)-N,N′-bis(phenyl)benzidine (NPB) or the 1-(3-methylphenyl)-1,2,3,4-tetrahydroquinoline-6-carboxyaldehyde-1,1′-diphenylhydrazone (MTCD) as hole-transporting layer, the DIP layer as an emitting layer and the tris(8-hydroxyquinoline aluminum) (Alq3) as the electron transporting layer. All the organic layers were sequentially deposited in a high vacuum by thermal evaporation onto indium tin oxide substrates and without breaking vacuum. Continuous electroluminescence emission was obtained in all configurations upon varying the applied bias voltage from 4 to 30 V, the observed wide emission band was centered at 493 nm. The luminance of the devices was about 1500 (cd)/m2 with 4.5 cd/A of efficiency for the best device. The charge transport behavior in the OLED is also discussed as a function of different carrier injection levels.  相似文献   

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A memory functionality is a prerequisite for many applications of electronic devices. Organic nonvolatile memory devices based on ferroelectricity are a promising approach toward the development of a low‐cost memory technology. In this Review Article we discuss the latest developments in this area with a focus on three of the most important device concepts: ferroelectric capacitors, field‐effect transistors, and diodes. Integration of these devices into larger memory arrays is also discussed.  相似文献   

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The use of micrometer and nanometer‐sized organic single crystals to fabricate devices can retain all the advantages of single crystals, avoid the difficulties of growing large crystals, and provide a way to characterize organic semiconductors more efficiently. Moreover, the effective use of such “small” crystals will be beneficial to nanoelectronics. Here we review the recent progress of organic single‐crystalline transistors based on micro‐/nanometer‐sized structures, namely fabrication methods and related technical issues, device properties, and current challenges.  相似文献   

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Currently there is great interest in using organic semiconductors to develop novel flexible electronic applications. An emerging strategy in organic semiconductor materials research involves development of composite or layered materials in which electronic and ionic conductivity is combined to create enhanced functionality in devices. For example, we and other groups have employed ionic motion to modulate electronic transport in organic field‐effect transistors using solid electrolytes. Not only do these transistors operate at low voltages as a result of greatly enhanced capacitive coupling, but they also display intriguing transport phenomena such as negative differential transconductance. Here, we discuss differences in operation between traditional (e.g., SiO2) and electrolyte‐based dielectrics, suggest further improvements to currently used electrolyte materials, and propose several possibilities for exploiting electrolytes in future applications with both organic and inorganic semiconductors.  相似文献   

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Stretchable electronics are essential for the development of intensely packed collapsible and portable electronics, wearable electronics, epidermal and bioimplanted electronics, 3D surface compliable devices, bionics, prosthesis, and robotics. However, most stretchable devices are currently based on inorganic electronics, whose high cost of fabrication and limited processing area make it difficult to produce inexpensive, large‐area devices. Therefore, organic stretchable electronics are highly attractive due to many advantages over their inorganic counterparts, such as their light weight, flexibility, low cost and large‐area solution‐processing, the reproducible semiconductor resources, and the easy tuning of their properties via molecular tailoring. Among them, stretchable organic semiconductor devices have become a hot and fast‐growing research field, in which great advances have been made in recent years. These fantastic advances are summarized here, focusing on stretchable organic field‐effect transistors, light‐emitting devices, solar cells, and memory devices.  相似文献   

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Organic light‐emitting diodes fabricated by subsequently spin‐coating two layers—a hole‐transporting followed by a metal chelate emissive layer—onto poly(3,4‐ethylenedioxythiophene)/poly(styrenesulfonate) are presented for the first time. The electron–hole recombination occurs in a layer consisting of Ga complexes (see Figure), which exhibit high fluorescence quantum yields, and their emission spectra are blue‐shifted relative to that of tris(8‐hydroxyquinoline) aluminum. By doping this spin‐coated emission layer with fluorescent emitters the emission band can be shifted within the visible spectral range.  相似文献   

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