Control of carrier density by self-assembled monolayers in organic field-effect transistors

Organic thin-film transistors are attracting a great deal of attention due to the relatively high field-effect mobility in several organic materials. In these organic semiconductors, however, researchers have not established a reliable method of doping at a very low density level, although this has been crucial for the technological development of inorganic semiconductors. In the field-effect device structures, the conduction channel exists at the interface between organic thin films and SiO(2) gate insulators. Here, we discuss a new technique that enables us to control the charge density in the channel by using organosilane self-assembled monolayers (SAMs) on SiO(2) gate insulators. SAMs with fluorine and amino groups have been shown to accumulate holes and electrons, respectively, in the transistor channel: these properties are understood in terms of the effects of electric dipoles of the SAMs molecules, and weak charge transfer between organic films and SAMs.     

Carrier control of graphene driven by the proximity effect of functionalized self-assembled monolayers

We demonstrated the carrier control of graphene by employing the electrostatic potential produced by several types of self-assembled monolayer (SAM) formed on SiO(2) substrates. For single layer graphene on perfluoroalkylsilane-SAM, the stiffening of the Raman G-band indicates a large down shift of the Fermi level (～-0.8 eV) by accumulated hole carriers. Meanwhile, aminoarylsilane-SAM accumulated electron carriers, which compensate the hole carriers doped by adsorbed molecules under the ambient atmosphere, in graphene. The present results and their theoretical analysis reveal that the use of the dipole moments of SAM molecules can systematically modulate the electrostatic potential affecting graphene without destroying its intrinsic electronic structure and let us know that the proximity effect of the SAMs is a promising way in developing graphene-based solid state electronics.     

基于芘丁酸的SAMs薄膜制备及荧光氧猝灭特性

利用SAMs(self-assembled monolayers)技术将芘丁酸分子接枝于经过3-氨丙基三乙氧基硅烷分子(APTES)修饰的玻璃基片表面。通过XPS、荧光发射光谱的表征以及接触角测试等来考察薄膜的结构及性能,考察了薄膜在不同溶剂中的荧光氧猝灭特性。实验表明,芘丁酸分子以化学键合的方式固定于玻片表面,形成了SAMs薄膜,其在甲苯、三氯甲烷、二氯甲烷等极性较小的有机溶剂中的氧猝灭效率较高,并具有良好的重复性。     

Immobilisation of cobaltferritin onto gold electrode based on self-assembled monolayers

The iron storage protein, ferritin, has a cavity of ～7?nm in diameter in which iron is oxidised and stored as a hydrated oxide core. Electron transfer is known to be an important step in the sequestering of iron by cellular ferritin. The cavity was used as a nanocontainer to grow cobalt nanoparticles. The immobilisation of ferritin on the electrode surface is essential for various bioelectronic applications. A cobaltferritin-immobilised electrode based on self-assembled monolayer (SAM)-modified gold electrode was developed. The cobaltferritin-immobilised SAM-modified electrode was characterised by electrochemical and atomic force microscopy (AFM) techniques. The results indicated that cobaltferritin was selectively immobilised onto succinimidyl alkanedisulfide-modified Au electrode by the covalent interaction between cobaltferritin and the terminal functional groups of the SAMs. The cobaltferritin immobilised modified electrode showed a direct electron transfer reaction between cobaltferritin and the electrode. The electrochemically regulated uptake and release of cobalts for cobaltferritin immobilised on the SAMs were demonstrated. The results obtained in this study indicate that cobaltferritin has potential for a biomaterial in nanoscale synthesis for potential magnetic, catalytic and biomedical-sensing applications.     

高浓度石墨烯水系分散液及其气液界面自组装膜

通过测试石墨烯分散液的吸光度,比较了几种表面活性剂分散石墨烯的能力.结果表明:聚乙烯吡咯烷酮(PVP)这种"绿色"、低成本的表面活性剂,具有很好的分散能力.通过提高PVP溶液浓度,可以得到浓度高达～1.3mg/mL的石墨烯分散液,这种高浓度石墨烯分散液可以在气液界面自组装得到石墨烯膜,这种无支撑石墨烯膜具有平整的表面和规则的结构,在很多领域都有良好的潜在应用价值.     

Antibody arrays prepared by cutinase-mediated immobilization on self-assembled monolayers

Antibody arrays hold considerable potential in a variety of applications including proteomics research, drug discovery, and diagnostics. Many of the schemes used to fabricate the arrays fail to immobilize the antibodies at a uniform density or in a single orientation; consequently, the immobilized antibodies recognize their antigens with variable efficiency. This paper describes a strategy to immobilize antibodies in a single orientation, with a controlled density, using the covalent interaction between cutinase and its suicide substrate. Protein fusions between cutinase and five antibodies of three different types (scFv, V(HH), and FN3) were prepared and immobilized upon self-assembled monolayers (SAMs) presenting a phosphonate capture ligand. The immobilized antibodies exhibit high affinity and selectivity for their target antigens, as monitored by surface plasmon resonance and fluorescence scanning. Furthermore, by changing the density of capture ligand on the SAM the density of the immobilized antibody could be controlled. The monolayers, which also present a tri(ethylene glycol) group, are inert to nonspecific adsorption of proteins and allow the detection of a specific antigen in a complex mixture. The demonstration of cutinase-directed antibody immobilization with insert SAMs provides a straightforward and robust method for preparing antibody chips.     

Forming microstructured alkanethiol self-assembled monolayers on gold by laser ablation

A process to form microstructured alkanethiol self-assembled monolayers (SAMs) on gold is described. It is well known that alkanethiols spontaneously form homogenous SAMs on gold surfaces. By means of laser ablation, the exposed areas of alkanethiol monolayers can be removed from the gold surface. Free gold is obtained which can react further with second and third thiols. By this technique, structured alkanethiol SAMs are obtained reliably and easily. In a rather narrow window of pulse intensities, in our example 120$hboxMW/cm^2pm hbox10%$from a frequency-doubled Nd : YVO$_4$laser with 6-ns pulsewidth operating at a repetition rate of 20 kHz, ablation of alkanethiol monolayers is obtained without causing any damage to the gold substrate. Examples are presented where lines down to 10$muhbox m$in width were laser ablated into an SAM formed either from a hydrophilic or a hydrophobic alkanethiol and filled with a monolayer of a second alkanethiol of opposite hydrophilicity. The patterned structures were examined by optical and fluorescence microscopy as well as by lateral force microscopy. The presented method enables the preparation of microstructured SAMs on gold and probably on a wide variety of other substrates.     

Synthesis of hydroxyapatite on titanium coated with organic self-assembled monolayers

The work focuses the formation of hydroxyapatite (HA) layers from simulated body fluids (SBF) onto titanium coated with NH₂-, SH-, and SO₃H-SAMs, respectively, at room temperature and 37 °C as well as pH values of SBF of 7.4, 8, and 8.4. At an upside up arrangement of the samples in the SBF, the formation of sufficient thick HA layers with a pillow like structure onto all SAMs were observed, which is believed to be caused by combined homogeneous and heterogeneous precipitation of HA from the SBF. These layers do not show sufficient adhesive strength. An upside down arrangement of the samples result in the formation of up to 5–10 μm thick flat HA layers with a much higher adhesive strength, which is believed to be due to formation of HA from the SBF only by heterogeneous precipitation. Also HA layers were obtained onto all studied SAMs, SH-SAM appears to favour the formation of HA resulting in a layer with a thickness of about 10 μm and an almost stoichiometric Ca/P-ratio of the layer of 1.72. All other layers exhibit much lower ratios.     

A self-assembled Ag nanoparticle agglomeration process on graphene for enhanced light output in GaN-based LEDs

We introduce Ag nanoparticles fabricated by a self-assembled agglomeration process in order to enhance the electrical properties, adhesive strength, and reliability of the graphene spreading layer in inorganic-based optoelectronic devices. Here, we fabricated InGaN/GaN multi-quantum-well (MQW) blue LEDs having various current spreading layers: graphene only, graphene with Ag nanoparticles covering the surface, and graphene with Ag nanoparticles only in selectively patterned micro-circles. Although the Ag nanoparticles were found to act as an additional current path that increases the current spreading, optical properties such as transmittance also need to be considered when the Ag nanoparticles are combined with graphene. As a result, LEDs having a graphene spreading layer with Ag nanoparticles formed in selectively patterned micro-circles displayed more uniform and stable light emission and 1.7 times higher light output power than graphene only LEDs.     

High-performance carbon nanotube field effect transistors with a thin gate dielectric based on a self-assembled monolayer

Individual single-walled carbon nanotube (SWCNT) field effect transistors (FETs) with a 2 nm thick silane-based organic self-assembled monolayer (SAM) gate dielectric have been manufactured. The FETs exhibit a unique combination of excellent device performance parameters. In particular, they operate with a gate-source voltage of only -1 V and exhibit good saturation, large transconductance, and small hysteresis (相似文献   

Mixed-valence manganese oxide/reduced graphene oxide composites with enhanced pseudocapacitive performance

Journal of Materials Science - As typical pseudocapacitive materials, manganese oxides have attracted great interest due to their high theoretical specific capacitance, abundant oxidation states...     

Stretchable graphene transistors with printed dielectrics and gate electrodes

With the emergence of human interface technology, the development of new applications based on stretchable electronics such as conformal biosensors and rollable displays are required. However, the difficulty in developing semiconducting materials with high stretchability required for such applications has restricted the range of applications of stretchable electronics. Here, we present stretchable, printable, and transparent transistors composed of monolithically patterned graphene films. This material offers excellent mechanical, electrical, and optical properties, capable of use as semiconducting channels as well as the source/drain electrodes. Such monolithic graphene transistors show hole and electron mobilities of 1188 ± 136 and 422 ± 52 cm(2)/(V s), respectively, with stable operation at stretching up to 5% even after 1000 or more cycles.     

A novel contact engineering method for transistors based on two-dimensional materials

Contact engineering is of critical importance for two-dimensional (2D) transition metal dichalcogenide(TMD)-based devices. However, there are only a few solutions to overcome this obstacle because of the complexity of the TMD-contact interface. In this work, we propose a novel method using a soft plasma treatment followed by the seamless deposition of a metal electrode to reduce the contact resistance of MoS_2 field effect transistors(FETs). The treated FETs exhibit three times higher mobility than the control FETs without plasma treatment. The soft plasma treatment can remove the facial sulfur atoms and expose the middle Mo atoms so that they come into direct contact with the metal electrode, thus greatly improving the contact behavior. First-principles calculation is also performed to support the experimental results. Our potentially scalable strategy can be extended to the whole family of TMD based FETs to provide a possible route of device processsing technology for 2D device application.     

A review on mechanisms and recent developments of nanomaterials based carbon fiber reinforced composites for enhanced interface performance

Carbon fiber reinforced composites have attracted lots of attention in many fields. However, on account of the poor infiltration of resin to carbon fiber, the weak interface performance between fiber and resin has been restricting the interface properties of composites. In recent progress, the review attaches more importance to the introduction of the third phase monomer, which mainly uses physical and chemical methods to assemble nanomaterials (such as carbon nanotubes, graphene, etc.) on the carbon fiber surface to modify the interface structure of the carbon fiber reinforced composites, and all of them have been demonstrated in this paper. Furthermore, the effects of introducing nanomaterials on the structure of the fiber/resin interface and the relationship between multi-scale interface structure and properties have been investigated. It can be seen that the design idea of researchers mainly uses one or more theories to improve the interface properties of carbon fiber reinforced composites, such as transition layer, chemical bonding, mechanical interlocking, infiltration, diffusion, and adsorption. In brief, this work provides some novel insights for the preparation of carbon fiber reinforced composites with excellent interlaminar shear strength.