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111.
In this work, a comparison of the interfacial electronic properties between a semiconducting oligomer and a variety of substrates with different properties—metal, semiconductor and oxide layers—is reported. The interface formation was studied by X-ray and Ultraviolet photoelectron spectroscopies (XPS, UPS). High purity oligomer films with thickness up to 10 nm were prepared by stepwise evaporation on the clean substrates under ultrahigh vacuum (UHV) conditions. Analysis of the oligomer and substrate related XPS spectra clarified the interfacial chemistry and band bending in the semiconducting materials. The valence band structure and the interfacial dipoles were determined by UPS. The barriers for hole injection were measured at the interfaces of the organic film with all substrates. The interfacial energy band diagrams were deduced in all cases from the combination of XPS and UPS results. Emphasis was given on the influence of the substrate work function (eΦ) on the electronic properties of these interfaces. 相似文献
112.
113.
《Solid State Ionics》2006,177(35-36):3161-3170
A simple fatigue model for perovskite ferroelectrics is developed based on electric field driven point defect drift. At room temperature significant point defect cluster growth only occurs if diffusion is enhanced by an electrically supported drift mechanism. In order to achieve a significant charge carrier drift considerable parts of the depolarizing field have to be temporarily unscreened. These unscreened local environments can only occur under a bipolar duty cycle just before complete reversal of the domain system. The case of the oxygen vacancy as an ionic defect is modeled. 相似文献
114.
Cr-doped mullites were prepared from single-phase precursors containing up to 9.60 wt% Cr2O3 using a sol-gel technique followed by thermal treatment. Particle induced X-ray emission spectroscopy and X-ray powder diffraction were used to characterize the samples. Mullites were orthorhombic, space group Pbam. Cr doping caused the increase of unit-cell parameters. Strongest expansion was noticed along c-axis followed by a and b (Δc/c=0.089, Δa/a=0.061, Δb/b=0.045% per mole Cr2O3). A second phase, namely θ-(Al,Cr)2O3, was revealed by XRD in the sample containing 9.60 wt% Cr2O3. The structure of mullites was refined by the Rietveld method, location of Cr3+ was performed by the EPR spectroscopy. At low chromium doping level (Cr2O3 content less than ∼5 wt%) Cr3+ ions were substituted for Al3+ in the AlO6 octahedra of the mullite structure (M1 site). For higher doping level, Cr3+ ions were additionally substituted for Al3+ in the AlO6 octahedra of the second phase [θ-(Al,Cr)2O3 at 1400 °C, or α-(Al,Cr)2O3 at 1600 °C] which segregated in the system. Substitution of Cr3+ for Al3+ on M1 site in the mullite structure resulted in increase of average distances in (M1)O6 octahedron and decrease of average distances in T*O4 tetrahedron, while average distances in TO4 tetrahedron stayed almost constant. 相似文献
115.
B.-K. Kim H. Oh E.-K. Jeon S.-R. Kim J.-R. Kim J.-J. Kim J.-O. Lee C.J. Lee 《Applied Physics A: Materials Science & Processing》2006,85(3):255-263
This paper presents a review of our current experimental research on GaP nanowires grown by a vapor deposition method. Their structural, electrical, opto-electric transport, and gas-adsorption properties are reviewed. Our structural studies showed that a GaP nanowire consisted of a core–shell structure with a single-crystalline GaP core and an outer Ga2O3 layer. The individual GaP nanowires exhibited n-type field effects. Their electron mobilities were in the range of about 6 to 22 cm2/V s at room temperature. When the nanowires were illuminated with an ultraviolet light source, an abrupt increase of conductance occurred resulting from carrier generation in the nanowire and de-adsorption of adsorbed OH- or O2
- ions on the Ga2O3 surface shell. Using an intrinsic Ga2O3 shell layer as a gate dielectric, top-gated GaP nanowire field-effect transistors were fabricated and characterized. Like other metal oxide nanowires, the carrier concentration and mobility of GaP nanowires were significantly affected by the surface molecular adsorption of OH or O2. The GaP nanowire devices were fabricated as sensors for NO2, NH3, and H2 gases by using a simple metal decoration technique. PACS 73.63.-b; 72.80.Ey; 85.35.-p 相似文献
116.
The influence of additives such as TiO2, Al2O3 and their mechanical mixture as well as aluminium oxide, the surface of which contains phosphorous and titanium-oxide nanostructures, on the combustibility of foam plast (trade mark PEN-I), produced on the basis of epoxide novolak block-copolymers, was studied. It was stated that the incorporation both phosphorous-containing and titanium-containing oxides in the composition results in significant (in two to five times) decreasing of the samples’ combustibility. The probable mechanism of inhibition of burning process for those combustion retarders was discussed. 相似文献
117.
Calcium lanthanide oxyborate doped with rare-earth ions LnCa4O(BO3)3:RE3+ (LnCOB:RE, Ln=Y, La, Gd, RE=Eu, Tb, Dy, Ce) was synthesized by the method of solid-state reaction at high temperature. Their fluorescent spectra were measured from vacuum ultraviolet (VUV) to visible region at room temperature. Their excitation spectra all have a broadband center at about 188 nm, which is ascribed to host absorption. Using Dorenbos’ and Jφrgensen's work [P. Dorenbos, J. Lumin. 91 (2000) 91, R. Resfeld, C.K. Jφrgensen, Lasers and Excite States of Rare Earth [M], Springer, Berlin, 1977, p. 45], the position of the lowest 5d levels E(Ln,A) and charge transfer band Ect were calculated and compared with their excitation spectra.Eu3+ and Tb3+ ions doped into LnCOB show efficient luminescence under VUV and UV irradiation. In this system, Ce3+ ions do not show efficient luminescence and quench the luminescence of Tb3+ ions when Tb3+ and Ce3+ ions are co-doped into LnCOB. GdCOB doped with Dy3+ shows yellowish white light under irradiation of 254 nm light for the reason that Gd3+ ions transfer the energy from itself to Dy3+. Because of the existence of Gd3+, the samples of GdCOB:RE3+ show higher excitation efficiency than LaCOB:RE3+ and YCOB:RE3+, around 188 nm, which indicates that the Gd3+ ions have an effect on the host absorption and can transfer the excitation energy to the luminescent center such as Tb3+, Dy3+ and Eu3+. 相似文献
118.
Enantioselective olefin epoxidation using novel biphenyl and binaphthyl azepines and azepinium salts
《Tetrahedron: Asymmetry》2006,17(16):2334-2338
Homologous biphenyl and (diastereomeric) binaphthyl tertiary azepines and quaternary iminium salts were prepared from (S)- and (R)-3,3-dimethylbutan-2-amine. Both the amines and iminium ions behave as effective catalysts for the enantioselective epoxidation of unfunctionalized olefins (ee up to 87%). 相似文献
119.
不同方法制备的CO2-3替换磷灰石固溶体晶体化学的FTIR研究 总被引:1,自引:0,他引:1
采用不同方法制备了CO2-3替换的磷灰石固溶体,利用FTIR结合XRD对其进行了晶体化学研究,结果表明均相沉淀法制备的碳羟磷灰石(CHAP)属B型替换且替换方式是[CO3·OH]四面体替换[PO4]四面体;固相离子交换法制备的CHAP属A型替换且替换方式是[CO3]三角形配位体替换通道位置的OH-;固相反应法制备的碳氟磷灰石(CFAP)属B型替换,其替换方式是[CO3·F]四面体替换[PO4]四面体;sol-gel法制备的CHAP属AB混合型替换,其Ψ3分裂为Ψ3-1,Ψ3F,Ψ3-4.高斯函数法拟合表明Ψ3F峰是A型替换的Ψ3-2与B型替换的Ψ3-3的叠合.当WCO2-3<3.34%时,随CO2-3含量增加,A型替换量增大,且当WCO2-3=3.34%时达最大值,当3.34%<WCO2-3<7.52%时,随CO2-3含量增加,B型替换量增大,且当WCO2-3= 7.52%时亦到饱和. 相似文献
120.
P. Periasamy K. Tatsumi N. Kalaiselvi M. Shikano T. Fiyieda Y. Saito T. Sakai M. Mizukata A. Kajinami S. Deki 《Ionics》2002,8(5-6):453-460
A series of gel polymer electrolytes containing PVdF as homo polymer, a mixture of 1:1 Ethylene Carbonate (EC) : Propylene
Carbonate (PC) as plasticizer and lithium-bistrifluoromethane sulphone imide [imide — LiN (CF3SO2)2] has been developed. Amounts of polymer (PVdF), plasticizer and the imide lithium salt have been varied as a function of
their weight ratio composition in this regard. Dimensionally stable films possessing appreciable room temperature conductivity
values have been obtained with respect to certain weight ratio compositions. However, conductivity data have been recorded
at different possible temperatures, i.e., from 20 °C to 65 °C. XRD and DSC studies were carried out to characterize the polymer
films for better amorphicity and reduced glass transition temperature, respectively. The electrochemical interface stability
of the PVdF based gel polymer electrolytes over a range of storage period (24 h – 10 days) have been investigated using A.C.
impedance studies. Test cells containing Li/gel polymer electrolyte (GPE)/Li have been subjected to undergo 50 charge-discharge
cycles in order to understand the electrochemical performance behaviour of the dimensionally stable films of superior conductivity.
The observed capacity fade of less than 20% even after 50 cycles is in favour of the electrochemical stability of the gel
polymer electrolyte containing 27.5% PVdF −67.5 % EC+PC −5% imide salt. Cyclic voltammetry studies establish the possibility
of a reversible intercalation — deintercalation process involving Li+ ions through the gel polymer electrolyte. 相似文献