Abstract:
A molecular electronic device including an organic dielectric thin film and a method for fabricating the same are provided to block a penetrated electrode material from reaching a bottom electrode by increasing a distance from a molecular active layer to the bottom electrode. A molecular electronic device includes a substrate, an organic dielectric thin film(150) formed on the substrate, a molecular active layer(160) formed on the organic dielectric thin film and having a charge trap site, and an electrode(110) formed on the molecular active layer. The organic dielectric thin film comprises a molecular structure represented by M-R-T, wherein M is a sulfur-containing group or a silicon-containing group, R is a saturated or unsaturated C1 to C20 hydrocarbon group which is saturated or unsaturated with fluorine, and T is -SH, -NH2, or -COOH.
Abstract:
A compound for a molecular electronic device, a method for preparing the compound, and a molecular electronic device using the compound are provided to improve the coverage of a self-assembled molecular monolayer and to allow the thickness of a molecular active layer. A compound for a molecular electronic device comprises a ruthenium-terpyridine disulfide complex represented by the formula 2, wherein R1 and R2 are a C1-C20 saturated or unsaturated hydrocarbon group substituted or unsubstituted with F, respectively. A molecular electronic device comprises a first electrode; a second electrode; and a molecular active layer which is interposed between the two electrodes and has a structure formed by the self-assembling of the compound of the formula 2 on the first electrode.
Abstract:
트리아진 그룹으로 이루어지는 CF 화합물 (PFPT)로 구성되는 유기 화합물층을 포함하는 유기 전계발광 소자에 관하여 개시한다. 본 발명에 따른 유기 전계발광 소자는 2개의 전극과, 이들 사이에 형성된 적어도 하나의 유기 화합물층을 포함하고, 상기 유기 화합물층은 다음 식으로 표시되는 트리아진 유도체 화합물이 도핑되어 있다.
식중, R 1 , R 2 , 및 R 3 는 각각 퍼플루오로페닐렌 (perfluorophenylene) 유도체이다. 퍼플루오로페닐 트리아진, 유기 전계발광 소자, PFPT, 도핑
Abstract:
A method of manufacturing an organic molecular device is provided to improve the reproductivity of manufacturing processes by checking easily an adsorption degree of conductive organic molecules using the amount of current between an upper and a lower electrode. A lower electrode(43) is formed on a substrate(41). A sacrificial pattern(44) for enclosing the lower electrode is formed on the substrate. An upper electrode(45) is formed along an upper surface of the resultant structure. A nano gap(46) is formed between the lower and upper electrodes by removing the sacrificial pattern therefrom. Conductive organic molecules(47) are adsorbed onto the lower and upper electrodes within the nano gap.
Abstract:
PURPOSE: Provided are various spirobifluorene compounds with alkyl substituents at desired positions and their preparation method, thereby preparing derivatives each having different functions and excellent solubility to be used for polymer synthesis and as electronic materials. CONSTITUTION: Spirobifluorene compound is represented by the formula(1), wherein R1 and R2 are the same or different each other, and represent a C1-C20 linear or branched alkyl group or alkoxy group, or a thioalkyl group; and X1 and X2 are the same or different each other and represent hydrogen or halogen, or a hydroxyl group, or bone or boric ester, provided that X1 and X2 don't represent hydrogen simultaneously.
Abstract:
PURPOSE: A novel 4-sulfanylalkyl-3,5-dinitrobenzyl alcohol compound and its preparation method are provided, to obtain a compound useful as a molecular electron acceptor and applicable to a molecular electronic material. CONSTITUTION: The 4-sulfanylalkyl-3,5-dinitrobenzyl alcohol compound is represented by the formula 1, wherein R is H, an alkyl group or an acetyl group; and n is an integer of 1-25. The method comprises the steps of reacting p-methylbenzoic acid with nitric acid to prepare p-methyl-3,5-dinitrobenzoic acid; reacting the p-methyl-3,5-dinitrobenzoic acid with an alkyl alcohol in the presence of a catalyst to prepare an alkyl p-methyl-3,5-dinitrobenzoate; reacting the alkyl p-methyl-3,5-dinitrobenzoate with an N-halosuccinimide to prepare an alkyl 4-halomethyl-3,5-dinitrobenzoate; converting the ester group of the alkyl 4-halomethyl-3,5-dinitrobenzoate into an alcohol group in the presence of a catalyst to prepare a 4-halomethyl-3,5-dinitrobenzyl alcohol; and reacting the 4-halomethyl-3,5-dinitrobenzyl alcohol with potassium thioacetate or an alkyl thiosodium to prepare a compound whose R is an alkyl or acetyl group or removing the alkyl or acetyl group to prepare a compound whose R is H.
Abstract:
PURPOSE: A method of patterning an indium tin oxide layer on a plastic thin film and a rotary coater used for the method are provided to coat photoresist in uniform thickness and prevent undercut generated in the event of wet etching. CONSTITUTION: An ITO layer(11) is formed on a plastic substrate(10), and photoresist is coated on the ITO layer. Heat treatment is performed in order to remove a solvent contained in the coated photoresist. Ultraviolet rays are irradiated on a portion of the ITO layer, which is etched, using a patterned mask. The exposed portion of the photoresist is developed. Heat treatment is carried out to eliminate moisture and solvent left in the photoresist. The ITO layer is dipped in an ITO etchant using the patterned photoresist as a mask to wet-etch the ITO layer. The photoresist used as the mask is stripped.
Abstract:
PURPOSE: A method for fabricating a molecular electronic device is provided to reduce a manufacturing cost by using a single crystal growth method and a selective etching method. CONSTITUTION: The first semiconductor layer(20), the second semiconductor layer, and the third semiconductor layer(40) are sequentially laminated on a substrate(10). A nanogap(35) is formed between the first semiconductor layer(20) and the third semiconductor layer(40) by etching a side of the second semiconductor layer. A metal layer is formed on a surface of the resultant. An upper part(50a) and a lower part(50b) of the resultant is electrically disconnected to each other by cutting vertically the substrate(10). A molecular electronic element(70) is coated on the upper part(50a) and the lower part(50b) near to the nanogap(35).
Abstract:
In the organic electroluminescence (EL) device containing a bis-condensed derivative of 4-(dicyanomethylene)-2-methyl-6-(para-(dimethylaminostyryl)-4H-pyran, and the preparation thereof, the inventive organic electroluminescence device has a high luminescent efficiency and color coordinates based on a high purity, and is further simple in a synthesis and is prominent in a thermal stability, thereby providing great merits to a mass production of the organic electroluminescence device.