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71.
72.
Yu Zhai 《Archiv der Mathematik》2016,107(2):167-171
In this paper, we give a method of constructing conformal mappings defined in the unit disk which can fix arbitrarily many points on the unit circle. 相似文献
73.
Liu Haiqing Wang Xiangwei Kuang Chunxia Li Lei Zhai Yunyun 《Journal of Solid State Electrochemistry》2018,22(11):3579-3587
Journal of Solid State Electrochemistry - Ionic conductivity is an important separator parameter influencing the cycle life and rate capability of lithium-ion batteries (LIBs). To improve the ionic... 相似文献
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Yong Yang Su Zhi Ming Li Hong Bo Dong Guo Qing Zhou Li Hua Zhai Jiang Xu 《International journal of environmental analytical chemistry》2013,93(5):473-483
An ambient aerosol concentration enrichment system coupled with ICP-MS for real-time monitoring of airborne radioactive particles is now under development. ICP-MS is very sensitive to sample introduction conditions, so it is necessary to develop an easy-use calibration method for on-line quantitative analysis in field application. In this paper, a calibration method using standard solution instead of monodisperse particles was established and validated preliminarily. First of all, four parameters for the method were determined experimentally, including: uptake flow rate and nebulisation efficiency of the Microconcentric nebuliser, nebulisation/transport efficiency of Aridus Desolvating Sample Introduction System, and Relative Sensitivity Factor between 159?Tb and 174?Yb. Then, monodisperse terbium nitrate particles were generated by a commercial Vibrating Orifice Aerosol Generator. Continuous aerosols of ytterbium nitrate droplets were nebulised from standard solution. They were mixed together, desolvated through the membrane dryer and introduced into ICP-MS for on-line analysis of terbium nitrate particles. The air sampled from nuclear environment was also introduced into ICP-MS to investigate the effect of flow rate on instrument responses. Finally, atom numbers of 159?Tb in discrete terbium nitrate particles were determined using the calibration method and compared to the calculated value. Results show that when air flow rate increase from 10?mL?min?1 to 100?mL?min?1, the ratio of 159?Tb ion count to 174?Yb ion intensity keeps constant although instrument sensitivity decreases by a factor of 25. The relative standard deviation of 159?Tb atom number measured is better than 18%. The discrepancy with the calculated value could be attributed to the over-estimation of atom number in the particles generated by VOAG because there was some liquid leakage in the VOAG. 相似文献
76.
Some deviant breakdown-quenching characteristics of silicon photomultipliers are demonstrated and their physical mechanisms are explored. “Twice breakdown” phenomenon, “flat-topped” avalanche pulses and the determination method of the real breakdown voltage of the detector are analyzed. These characteristics are explained by the integration model in terms of avalanche threshold current based on the Haitz's equivalent circuit model. The reasoning results show that the maximum over-voltage for a normal operating silicon photomultiplier equals the product of the avalanche threshold current and the quenching resistor of the avalanche photo-diode (APD) pixel, approximately. Moreover, the model and results can be extended to other small avalanche junctions with quenching resistor. 相似文献
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78.
Jian-Ming Zhang Shang-Ru Zhai Bin Zhai Qing-Da An Ge Tian 《Journal of Sol-Gel Science and Technology》2012,64(2):347-357
Multifunctional nanomaterials with task-specific physicochemical properties, especially core?Cshell nanostructures with Fe3O4 core and NH2-functional shells (Fe3O4@SiO2?CNH2), have been extensively investigated as high-performance adsorbents, catalysts and catalyst supports; and in most cases the controllable sol?Cgel technique is the choice for fabrication of this kind of widely applied materials. Herein, we demonstrated that mono-dispersed and spherical Fe3O4@SiO2?CNH2 nanomaterials with magnetic response core, NH2-functional shell structure can be facilely prepared by co-condensation of TEOS with APTMS using a versatile sol?Cgel process. It was shown that the proper usage of APTMS and appropriate pre-hydrolysis time of TEOS were crucial and key steps for formation of highly uniform and desirable amino loading Fe3O4@SiO2?CNH2 materials. The TEOS pre-hydrolysis and the critical time (around 90?min) before the addition of APTMS prove to be vital for uniform structure evolution, while the appropriate concentration of APTMS (~2.28?mmol?L?1 in our system) leads to well-dispersed materials with relatively high loading of amino functionality. The as-prepared Fe3O4@SiO2?CNH2 magnetic nanoparticles prepared under optimum conditions possessing superparamagnetic behavior, uniform core?Cshell structure (~200?nm in diameter), relatively large BET surface area (~138?m2/g) and high incorporation of amino-functionality (~2.90?wt?%). 相似文献
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80.
Jie Gao Wan Song Peng Wang Guangqun Zhai 《Journal of polymer science. Part A, Polymer chemistry》2014,52(18):2562-2578
Kinetic results of CuSO4/2,2'‐bipyridine(bPy)‐amine redox initiated radical polymerization of methyl methacrylate (MMA) at 70 to 90 °C in dimethylsulfoxide suggest that such initiation is characteristic of a slow rate and a low initiator efficiency, but tertiary amines exhibit a relatively higher rate. UV‐Vis spectroscopy confirms the alpha‐amino functionality of PMMA chains. CuCl2/bPy successfully mediates the redox‐initiated radical polymerization of MMA with aliphatic tertiary amines in a fashion of slow‐initiated reverse atom transfer radical polymerization (ATRP), i.e. both the initiator efficiency of aliphatic tertiary amines and the average molecular weight of PMMA increase gradually, while the molecular weight distribution remains narrow but become broader with the conversions. As the PMMA chains contain alpha amino and omega C‐Cl moieties, UV‐induced benzophenone‐initiated radical polymerization and CuICl/bPy‐catalyzed ATRP initiated from PMMA lead to block copolymers from terminal functionalities. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2562‐2578 相似文献