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241.
242.
本文借助XRD,红外光谱等分析手段,研究了金属-载体相互作用状态对Pd/ZnO半导体陶瓷气敏特性的影响,据此提出贵金属催化剂和半导体陶瓷在气敏特性中的共同作用机理。PdZn界面层是氢处理时半导体正离子和金属原子间的相互扩散及反应所致。可以认为金属-载体间的强相互作用(SMSI)能显著提高其气敏特性。  相似文献   
243.
I-V characteristics of both β-FeSi2/n-Si and β-FeSi2/p-Si were studied at room temperature. The junctions were formed by depositing Fe on Si selectively followed by thermal annealing and some samples were later treated by pulsed laser. Temperature of thermal annealing and diode area were also varied.I-V studies on all these samples were done and ideality factors were computed. Results obtained were interpreted. Paper presented at the 5th IUMRS ICA98, October 1998, Bangalore.  相似文献   
244.
The conducting properties for holes and electrons of a set of 16 poly(arylenethynyl-thienoacene) derivatives as candidates for organic semiconductors have been theoretically studied at density functional theory (DFT) level. Some of the selected compounds show adequate values of charge carrier mobilities and injection parameters to be considered either p- or n-type organic semiconductors, although they all show high LUMO energy levels as compared to the Fermi level of Au electrode, decreasing their feasibility as ambipolar semiconductors. Derivatization with electron withdrawing moieties (F and CN) permits to suggest some of the studied compounds to display balanced both ease charge injection and high charge mobilities for holes and electrons, which could allow high performances as ambipolar semiconductors.  相似文献   
245.
模拟电路是电子信息类专业本科生的核心专业基础课程。课程中的内容涉及较多抽象概念,导致学生在理解和掌握上存在困难。通过让学生亲手测试相关器件的参数,能帮助学生更好理解抽象概念。但是,目前实验主要集中在电路,缺乏PN结和场效应晶体管等器件的实验测试条件。针对这一问题,提出利用基于二维半导体材料的PN结和场效应晶体管用于课程实验,加深学生对所学知识的理解和掌握。  相似文献   
246.
Transmission power cables are heated by conductor current. The morphology of the XLPE insulation may be changed by thermal aging. Disk-shaped insulating materials with semiconductive electrodes were used to understand this thermal effect against the dielectric breakdown strengths. The disk specimens were aged at 80 and 100°C before the breakdown strength measurements. These results showed that the dielectric breakdown strengths were improved with aging time. Analytical investigation of the insulating materials indicated that there were morphological changes such as increases of the lamella thickness and the spherulite diameter and decrease of the averaged lamella angle through heating. Cable specimens aged thermally with the same condition as the risk specimens also were observed with similar morphological changes in the insulation. Therefore it is concluded that the promotion of the crystallization by thermal aging is effective in improving the breakdown strength of the XLPE insulation unless it causes extreme deterioration.  相似文献   
247.
    
A series of donor–acceptor polymers incorporating the thieno[3,2‐b]thiophene‐2,5‐dione (TTD) acceptor unit and different donor units are synthesized. The synthesis of a TTD‐based key monomer, 3,6‐bis(5‐bromo‐4‐alkylthiophen‐2‐yl)thieno[3,2‐b]thiophene‐2,5‐dione, is successfully improved to afford higher total yield with less reaction steps (42%/4 steps) than those previously reported (14%/7 steps). The polymers exhibit low‐lying lowest unoccupied molecular orbital (LUMO) energy levels of around −3.8 eV and highest occupied molecular orbital (HOMO) energy levels ranging from −5.49 to −5.14 eV. Organic field‐effect transistors based on the polymers exhibit ambipolar characteristics with high hole and electron mobilities in the order of 10−1 cm2 V−1 s−1 in air. These high mobilities can be attributed to the formation of highly crystalline lamellar structure with preferential edge‐on orientation of the polymer thin films. Interestingly, the ratio of the electron to hole mobilities decreases with the extension of the donor units. This can be explained by the distribution of HOMOs and LUMOs along the backbones. Additionally, complementary inverters using the polymers with well‐balanced ambipolar characteristics exhibit sharp switching characteristics with high gain of ≈140 at the supply voltage of 40 V.  相似文献   
248.
    
Dye‐doped semiconducting polymers are used as active layers in polymer light‐emitting diodes (polyLEDs). The emission color can be tuned by doping the active polymer with certain dyes. This concept of energy transfer is demonstrated for a green matrix doped with a red‐emitting dye, suitable for use in LEDs. An absolute PL efficiency of 39% is observed for this system. Another very attractive development is taking place in the area of all‐polymer transistors. This may lead to a (partial) replacement of the driving electronics by all‐plastic circuits. A new precursor route toward poly(thienylenevinylene)s (PTVs), suitable as active material in all‐polymer integrated circuits, is presented. Synthesis of the precursors is reproducible and fast, and can readily be scaled for manufacture. Quantitative conversion of the precursor polymer can be accomplished by heating at 150°C for 20 min. The resulting mobility (6 × 10?3 cm2/V‐sec) and ON‐OFF ratio (4 × 104) makes this material a suitable candidate for the development and large‐scale manufacturing of all‐polymer integrated circuits.  相似文献   
249.
Improved efficiency in semiconducting polymer light-emitting diodes   总被引:1,自引:0,他引:1  
We report visible light emission from metal-polymer diodes made from semiconducting polymers, with indium-tin oxide as the “ohmic” contact, and a variety of metals as the barrier metal. Our results, which confirm the discovery by the Cambridge group [Nature347, 539 (1990)], demonstrate that light-emitting diodes can be fabricated by casting the polymer film on indium-tin oxide from solution with no subsequent polymer processing or heat treatment required. Electrical characterization reveals diode behavior with rectification ratios greater than 105 at sufficiently high voltages. Use of an electrode material with low work function leads to more than an order of magnitude improvement in the room-temperature efficiency of the devices. For example, the most efficient devices made with calcium as the rectifying contact display efficiencies of 0.01 photons per electron.  相似文献   
250.
    
Intra‐ and intermolecular ordering greatly impacts the electronic and optoelectronic properties of semiconducting polymers. The interrelationship between ordering of alkyl sidechains and conjugated backbones has yet to be fully detailed, despite much prior effort. Here, the discovery of a highly ordered alkyl sidechain phase in six representative semiconducting polymers, determined from distinct spectroscopic and diffraction signatures, is reported. The sidechain ordering exhibits unusually large coherence lengths (≥70 nm), induces torsional/twisting backbone disorder, and results in a vertically multilayered nanostructure with ordered sidechain layers alternating with disordered backbone layers. Calorimetry and in situ variable temperature scattering measurements in a model system poly{4‐(5‐(4,8‐bis(3‐butylnonyl)‐6‐methylbenzo[1,2‐b:4,5‐b′]dithiophen‐2‐yl)thiophen‐2‐yl)‐2‐(2‐butyloctyl)‐5,6‐difluoro‐7‐(5‐methylthiophen‐2‐yl)‐2H‐benzo[d][1,2,3]triazole} (PBnDT‐FTAZ) clearly delineate this competition of ordering that prevents simultaneous long‐range order of both moieties. The long‐range sidechain ordering can be exploited as a transient state to fabricate PBnDT‐FTAZ films with an atypical edge‐on texture and 2.5× improved field‐effect transistor mobility. The observed influence of ordering between the moieties implies that improved molecular design can produce synergistic rather than destructive ordering effects. Given the large sidechain coherence lengths observed, such synergistic ordering should greatly improve the coherence length of backbone ordering and thereby improve electronic and optoelectronic properties such as charge transport and exciton diffusion lengths.  相似文献   
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