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911.
Charlton C Gubala V Gandhiraman RP Wiechecki J Le NC Coyle C Daniels S Maccraith BD Williams DE 《Journal of colloid and interface science》2011,354(1):405-409
We report a method for studying nanoparticle-biosensor surface interactions based on total internal reflection fluorescence (TIRF) microscopy. We demonstrate that this simple technique allows for high throughput screening of non-specific adsorption (NSA) of nanoparticles on surfaces of different chemical composition. Binding events between fluorescent nanoparticles and functionalized Zeonor? surfaces are observed in real-time, giving a measure of the attractive or repulsive properties of the surface and the kinetics of the interaction. Three types of coatings have been studied: one containing a polymerized aminosilane network with terminal -NH(2) groups, a second film with a high density of -COOH surface groups and the third with sterically restraining branched poly(ethylene)glycol (PEG) functionality. TIRF microscopy revealed that the NSA of nanoparticles with negative surface charge on such modified coatings decreased in the following order -NH(2)>-branched PEG>-COOH. The surface specificity of the technique also allows discrimination of the degree of NSA of the same surface at different pH. 相似文献
912.
Yuan S Si H Fu A Chu T Tian F Duan YB Wang J 《The journal of physical chemistry. A》2011,115(5):940-947
Titanium silicalite-1 (TS-1) is an important catalyst for selective oxidation reactions. However, the nature and structure of the active sites and the mechanistic details of the catalytic reactions over TS-1 have not been well-understood, leaving a continuous debate on the genesis of active sites on the TS-1 surface in the literature. In this work, the location of Si vacancies and [Ti(OSi)(4)] and [Ti(OSi)(3)OH] sites in the MFI (Framework Type Code of ZSM-5 (Zeolite Socony Mobile-Five)) framework has been studied using a full ab initio method with 40T clusters with a Si:Ti molar ratio of 39:1. It was shown that the former four energetically favorable sites for Si vacancies are T6, T12, T4, and T8 and for Ti centers of [Ti(OSi)(4)] are T10, T4, T8 and T11, being partially the same sites. Whether by replacing Si vacancies or substituting the fully coordinated Si sites, the most preferential site for Ti is T10, which indicates that the insertion mechanism does not affect the favorable sites of Ti in the MFI lattice. For the defective [Ti(OSi)(3)OH] sites, it was found that the Si vacancy at T6 with a Ti at its neighboring T9 site (T6-def-T9-Ti pair) is the most energetically favorable one, followed by a T6-def-T5-Ti pair with a small energy gap. These findings are significant to elucidate the nature of the active sites and the mechanism of reactions catalyzed by TS-1 and to design the TS-1 catalyst. 相似文献
913.
Lee B Kang SH Kang D Lee KH Cho J Nam W Han OH Hur NH 《Chemical communications (Cambridge, England)》2011,47(40):11219-11221
A solid hydrazine was isolated as a crystalline powder by reacting aqueous hydrazine with supercritical CO(2). Its structure determined by single crystal X-ray diffraction shows a zwitterionic form of NH(3)(+)NHCO(2)(-). The solid hydrazine is remarkably stable but is as reactive as liquid hydrazine even in the absence of solvents. 相似文献
914.
Han KN Li CA Bui MP Pham XH Seong GH 《Chemical communications (Cambridge, England)》2011,47(3):938-940
We controlled the morphologies of zinc oxide (ZnO) nanostructures on single-walled carbon nanotube electrodes by an electrochemical deposition method and investigated the dependence of the electrocatalytic characteristics toward hydrazine on the different morphologies. ZnO nanorods provided high electrocatalytic activity with unique electrochemical behaviours, associated with the H(+) ion generated by the electro-oxidation of hydrazine. 相似文献
915.
Latifi R Tahsini L Kumar D Sastry GN Nam W de Visser SP 《Chemical communications (Cambridge, England)》2011,47(38):10674-10676
Density functional theory calculations on the reactivity of a Ni(II)-superoxo complex in C-H bond activation, aromatic hydroxylation and heteroatom oxidation reactions have been explored; the Ni(II)-superoxo complex is able to react with substrates with weak C-H bonds and PPh(3). 相似文献
916.
Jeong J Yun E Choi Y Jung HY Chung SJ Song NW Chung BH 《Chemical communications (Cambridge, England)》2011,47(38):10668-10670
Photochromic compound-conjugated fluorescent fullerene-silica nanoparticles prepared by the reverse-microemulsion method was utilized for photoswitchable cellular imaging by repeatable irradiation of ultraviolet and visible light. 相似文献
917.
Huang H Qu C Liu X Huang S Xu Z Zhu Y Chu PK 《Chemical communications (Cambridge, England)》2011,47(24):6897-6899
Controlled assembly of gold nanorods induced by Na(3)PO(4) leads to a significant amplification of localized surface plasmon resonance (LSPR) signals. The strong affinity between Au and Hg alters the coupled LSPR signals due to the amalgamation of Hg and Au. This allows detection of Hg in aqueous solutions with ultra-high sensitivity and excellent selectivity, without sample pretreatment. 相似文献
918.
Chen J Li C Eda G Zhang Y Lei W Chhowalla M Milne WI Deng WQ 《Chemical communications (Cambridge, England)》2011,47(21):6084-6086
We demonstrate a novel architecture of solar cell by incorporating graphene thin film in a quantum dot sensitized solar cell. Quantum dot sensitized nanorods with a graphene layer exhibited a 54.7% improvement comparing a quantum dot sensitized ZnO nanorods without graphene layer. A fill factor as high as ~62% was also obtained. 相似文献
919.
Wang M Meng G Huang Q Xu Q Chu Z Zhu C 《Chemical communications (Cambridge, England)》2011,47(13):3808-3810
A highly sensitive and selective fluorescence ratiometric sensor membrane for 2,3,3'-trichlorobiphenyl has been achieved, via depositing polypyrrole nanotubes (PPyNTs, the fluorescence indicator) in nano-porous anodic aluminium oxide (NPAAO) template and subsequently immobilizing fluorescein isothiocyanate (as an internal reference) onto the inner walls of the PPyNTs embedded in the NPAAO. 相似文献
920.
We demonstrate a method for constructing bifunctional nanostructures, which conjugate biochemical and electrocatalytic activities, on glassy carbon surfaces by decorating the carbon surfaces with both biologically active glucose oxidases and size-monodisperse Pt nanoparticles (less than 2 nm in diameter) utilizing only a single dendrimer layer. 相似文献