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971.
K. V. Satyanarayana Rao S. Sreepathi Rao U. V. Subba Rao 《Crystal Research and Technology》1992,27(6):875-881
TSDC of pure polyacrylamide films of thickness 22 μ grown by isothermal solution growth technique has been studied as a function of polarizing field and polarizing temperature at a constant heating rate of 0.09 K s1 In these studies only one TSDC peak was observed and the temperature corresponding to this peak was found to be independent of polarizing field strength but dependent on polarizing temperature. The activation energies, relaxation parameters and charge associated with the peak were evaluated. The origin of TSDC is discussed. 相似文献
972.
973.
温度/应变/扭曲三参量同时测量低成本传感系统 总被引:9,自引:3,他引:6
提出了一种利用布喇格光纤光栅反射光作信号源、高频CO2激光脉冲写入的长周期光纤光栅和超周期光纤光栅作传感器实现温度、应变和扭曲同时测量的全光栅型低成本强度解调传感方案.文中利用长周期光纤光栅边缘滤波效应实现了温度、应变和扭曲传感信号的实时解调.实验结果表明,其温度和应变的测量灵敏度分别为-0.211 dB/℃和-0.012 dB/10με;而扭曲率的测量灵敏度为0.4394 dB/(rad·m-1),是该法写入普通LPFG的4倍以上. 相似文献
974.
Tang Chak-yin Fan Jianping Tsui Chi-pong Lee Tai-chiu Chad Luen-chow Rao Bin 《Acta Mechanica Solida Sinica》2007,20(1):57-64
Shear damage may occur in the process of metal machining such as blanking and cutting, where localized shear deformation is developed. Experimental findings indicate that microscopic shear damage evolution in aluminium alloy 2024T3 (A1 2024T3) is a multi-stage mechanism, including particle cracking, micro-shear banding, matrix microcracking and coalescence of microcracks. This study is an attempt to use a set of equations to describe the multi-stage shear damage evolution in Al 2024T3. The shear damage variables in terms of multi-couple parameters of a power-law hardening material have been defined. An evolution curve of shearing damage has been calculated from experimental data. The values of the shear damage variable at different stages of damage have also been calculated. By making use of the findings, the relation between the microscopic shear damage evolution and the macroscopic shear response of the material has been discussed. 相似文献
975.
Colorimetric sensing strategies as a powerful point-of-care testing(POCT) tool have attracted significant interest in various chem/biosensing applications.Taking the excellent bare-eye-detectable signaling feature,nanozymes-based colorimetric sensors enable more potential applications and have been a new forefront in the colorimetric POCT analysis toward different target analytes.However,the low catalytic activity of nanozymes in most cases limits their practical application.Recent efforts demonstrate that the aggregation-induced nanozymes provide a general means to modulate nanozymes activity and enhance colorimetric sensing performances of some nanozymes-based colorimetric sensors.But there are few reports are explored to discuss and review such aggregation-induced nanozymes and their colorimetric sensing applications.To highlight the advances and progress in aggregation-induced nanozymes based colorimetric assays,we herein summary the fundamentals,classify and applications of this newlydeveloping field,focusing on the aggregation-induced activity enhancement of nanozymes(AIAEnanozymes) with a significant "signal-on" feature and aggregation-induced activity inhibition of nanozymes(AIAI-nanozymes) with a dramatical "signal-of" characteristics.Finally,we also propose the current challenges and the future prospects on both AIAE-nanozymes and AIAI-nanozymes. 相似文献
976.
Debanjan Bhattacharjee Parameswara Rao Alapati 《Molecular Crystals and Liquid Crystals》2017,648(1):66-76
This article represents the electrical studies of an interdigitated highly skewed N(4-n-pentyloxybenzylidene) 4-n-alkylaniline (5O.16) compound. Interestingly the compound is partially bent like and unsymmetrical in alkyl chain length. Dielectric and impedance spectroscopy studies indicate the coupling between the liquid crystal and the electrical field. Studies were carried out as a function of temperature as well as frequency. Semicircular nature of the Cole–Cole plots indicates the reorientation of the molecule with the applied field. Using the experimental data and the theoretically fitted results the effective equivalent model circuit was designed. Which used to explain the behavior of the compound under the external electric effect and the influence of the electrodes with different variable represent the resistor circuit. However, the effect of the conductivity of temperature and frequency are also reported. 相似文献
977.
Seddique M. Ahmed 《Journal of solution chemistry》2008,37(7):919-932
The chromaticity of poly(o-anisidine) (POAN) doped with different acids (HA), HA-doped POAN, has been studied by the spectrophotometric technique and
the results were substantiated by molecular mechanics (MM+) calculations. The observed absorbance decrease (λ around 720 nm, dark green coloration) with increasing concentration of the inorganic oxidizing agent (KMnO4) can be attributed to the oxidative hydrolysis mechanism. The oxidative hydrolysis constant (K
h) is highly dependent on the strength of the acid used. The HClO4-doped POAN matrix has the ability to store about 128.878 kJ⋅g−1 chromogenic energy (CE) at the wavelength 720 nm in a condensed lightweight form. MM+ calculations suggest that the potential
energy (PE) in kJ⋅mol−1 of the optimum molecular geometric (OMG) structure of the HClO4-doped POAN matrix is at least two (2.052) times more stable than the OMG of the base form (POAN-EB) of the POAN matrix. Kinetic
parameters of the oxidative hydrolysis reaction of the HA-doped POAN matrix were deduced from absorbance variations with time.
The results of computer-oriented kinetic analysis indicate that the rate-controlling step for HA-doped POAN oxidative hydrolysis
is governed by the Ginstling-Bronshein equation that represents three-dimensional diffusion (D4). Activation parameters for
the oxidative hydrolysis of the HClO4-doped POAN matrix were computed and discussed. 相似文献
978.
979.
980.
A density functional and ab initio theory investigation on M@B9 and M@B10 molecular wheels containing planar nona- and deca-coordinate heavy group 11, 12 and 13 metals (M=Ag, Au, Cd, Hg, In, Ti)
has been performed. These unusual clusters all prove to be true minima on the potential energy surfaces of the systems and
σ+π double aromatic in nature. The first two vertical one-electron detachment energies of M@B10− (M=Ag, Au) anions and first two ionization potentials of M@B9 (M=Ag, Au) and M@B10 (M=Cd, Hg) neutrals were calculated to aid future experiments. The cluster complexes designed in this work may expend the
domain of planar hyper-coordinate elements to include heavy group 11, 12, and 13 metals and serve as interesting candidates
to be targeted in experiments.
Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.
Supported by the National Natural Science Foundation of China (Grant No. 20873117) 相似文献