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11.
Thin film electrode materials are key components in the development of high rate, high capacity solid‐state Li‐ion batteries. Detailed knowledge of the epitaxial film/substrate(current‐collector) interface structures, which provides insights into epitaxial growth mechanisms and the effects of microstructure on electrochemical properties, is essential for efficient materials and device design. Here we report the epitaxial growth mechanism of a typical cathodic LiMn2O4 thin film by exploring the detailed structural and compositional variations in the vicinity of a film/substrate interface using state‐of‐the‐art scanning transmission electron microscopy. Direct observation of atom columns shows the epitaxial film forms an atomically flat and coherent heterointerface with the substrate, but that the crystal lattice is tetragonally distorted with a measurable compositional gradient from the interface to the crystal bulk. The growth mechanism is interpreted in terms of a combination of chemical and physicomechanical effects, namely a complex interplay between the internal Jahn‐Teller distortions induced by oxygen non‐stoichiometry and the lattice misfit strain.  相似文献   
12.
In 1977, Tagashira and colleagues reported that the center‐of‐mass drift velocity Wr of an electron swarm defined in time of flight (TOF) takes a larger value than the drift velocity Wv defined in pulsed Townsend (PT) when ionization collisions take place. At the same time, they explained that the larger values of Wr are caused by the ionization generation of electrons at the front side of extending swarm due to higher mean energy. In this paper, a new definition of virtual drift velocity in configuration space Wr defined in PT is proposed, and calculated data of drift velocities and related quantities such as ionization coefficients and ionization frequencies in Ar in a high E/N range are discussed relative to Tagashira's data. © 2006 Wiley Periodicals, Inc. Electr Eng Jpn, 155(2): 1–7, 2006; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20131  相似文献   
13.
This paper presents a two-degree-of-freedom (two-DOF) linear encoder which can measure the position along the moving axis (X-axis) and the straightness along the axis vertical to the moving axis (Z-axis) of a precision linear stage simultaneously. The two-DOF linear encoder is composed of a reflective-type scale grating and an optical sensor head. A reference grating, which is identical to the scale grating except the scale length, is employed in the optical sensor head. Positive and negative first-order diffracted beams from the two gratings are superposed with each other in the optical sensor head to generate interference signals. The optical configuration is arranged in such a way that the direction of displacement in each axis can also be detected. A prototype two-DOF linear encoder is designed and constructed. The size of the optical sensor head is about 50 mm (X) × 50 mm (Y) × 30 mm (Z) and the pitch of the grating is 1.6 μm. It has been confirmed that the prototype two-DOF linear encoder has sub-nanometer resolutions in both the X- and Z-axes.  相似文献   
14.
Poly(ethylene terephthalate) (PET) films possessing extremely enhanced hydrolytic stability were developed by combining the improved processes of polymerization, melt extrusion, and biaxial stretching. The PET films obtained from the combined process were better than commercially available PET films with highest hydrolytic stability at present. An accelerated test (at 120°C and 100% relative humidity) was performed to learn the key parameters governing elongation‐based hydrolytic durability of PET films. The results suggested that ultimate hydrolytic stability was because of the combined effects of significant decrease in the content of carboxylic acid terminal groups and enhanced crystallinity. Another reason for this was an increase in ground‐state dimer sites due to intermolecular stacking between terephthalate units. These dimer sites were probably located in the densely packed amorphous regions, as suggested from the intrinsic fluorescence spectrum of PET films. The PET films developed in this study are very useful in outdoor applications such as backsheet materials in solar cell modules. POLYM. ENG. SCI., 58:261–271, 2018. © 2017 Society of Plastics Engineers  相似文献   
15.
16.
This paper describes the results of tests and discussions carried out to develop a system for partial discharge monitoring in GIS. They include the propagation characteristics of partial discharge pulses in each GIS component, as well as the test results obtained using an actual 300‐kV GIS. We also report the results of verification test on the GIS partial discharge monitoring and location system developed by the authors. © 1999 Scripta Technica, Electr Eng Jpn, 129(2): 40–50, 1999  相似文献   
17.
Extremely long nanofibers, whose lengths reach the millimeter regime, are generated via co-aggregation of a melamine-appended perylene bisimide semiconductor and a substituted cyanurate, both of which are ditopic triple-hydrogen-bonding building blocks; they co-aggregate in an unexpected stoichiometrically mismatched 1:2 ratio. Various microscopic and X-ray diffraction studies suggest that hydrogen-bonded polymeric chains are formed along the long axis of the nanofibers by the 1:2 complexation of the two components, which further stack along the short axis of the nanofibers. The photocarrier generation mechanism in the nanofibers is investigated by time-of-flight (TOF) experiments under electric and magnetic fields, revealing the birth and efficient recombination of singlet geminate electron-hole pairs. Flash-photolysis time-resolved microwave conductivity (FP-TRMC) measurements revealed intrinsic 1D electron mobilities up to 0.6 cm(2) V(-1) s(-1) within nanofibers.  相似文献   
18.
The magnetic properties of high-silicon steel sheets ranging in thickness from 0.35 to 0.03 mm and silicon content from 3 to 7.5 percent is investigated. The minimum iron losses are obtained with the silicon higher than 6.5 percent at the high-frequency range over 30 kHz. The sheet thickness dependency index m is estimated. The heat treatment effects to soft magnetic properties also are studied.  相似文献   
19.
Sarcophytol A (SaA), a cembrane-type diterpene, inhibits pancreatic carcinogenesis induced by N-nitrosobis(2-oxypropyl)amine (BOP) in hamsters. The experimental groups received two injections of BOP at 70 mg/kg dose, followed 2 weeks later by a 20 mg/kg dose injection, and were fed a basal diet or 0.01 and 0.05% SaA diets starting 1 week after the second injection of BOP. Control groups were injected with normal saline and fed the basal diet or the 0.05% SaA diet. All animals were killed 30 weeks after the start of the experiments. Seventeen BOP-treated hamsters fed the basal diet developed pancreatic tumors (77.3%) while only 12 of 21 hamsters fed the 0.01% SaA diet (57.1%) and 12 of 23 hamsters fed the 0.05% SaA diet (52.2%) developed pancreatic tumors. Pancreatic lesions included ductal hyperplasia, atypical ductal hyperplasia, and carcinoma in situ. Microscopic invasive carcinoma induced by BOP and the incidence of larger pancreatic tumors in hamsters were significantly higher in hamsters fed the basal diet than in hamsters fed the SaA diet (p < 0.05). The proliferating cell nuclear antigen (PCNA) labeling index of pancreatic carcinoma in BOP-treated hamsters fed the basal diet was 41.2 +/- 13.4%, whereas BOP-treated hamsters fed 0.01 and 0.05% SaA diets yielded PCNA indexes of 26.8 +/- 8.3 and 28.4 +/- 7.0%, respectively. k-ras mutation was detected in 40% of cancers in both groups. No pancreatic tumors developed in saline-treated groups, and no differences in body weights or histological findings in their organs, including the pancreas, were observed in either group. These findings suggest that SaA not only inhibits BOP-induced pancreatic carcinogenesis in hamsters, but also provides antipromotion and antiprogression effects on these tumors, even when SaA commences 1 week after the initiation of pancreatic carcinogenesis.  相似文献   
20.
The optical properties of the thin films of asymmetrically substituted polysilane homopolymers and copolymers were studied. A conformational change in the organopolysilanes having (pentoxy,methyl) or (hexyl,methyl) groups was observed by polarized UV spectrometry and a wide angle X-ray diffraction. The polysilanes and polysilane copolymers having hexyl and pentoxy side chains were crystallized to form oriented films along the direction of the mechanically oriented polytetrafluoroethylene (PTFE) films. The bathochromic shifts were observed for polysilane and the polysilane copolymer having pentoxy side chains when the film thickness was small (ca. <50 nm). The influence of the thickness of the films on the spectral change was significant when the substituent was a pentoxy group, however, not when it was a hexyl group.  相似文献   
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