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21.
Olle Nilsson 《Journal of separation science》1982,5(1):38-44
The total length-based second moment contribution from longitudinal sample diffusion in both phases on a column, σD , is derived by adding individual partial differential contributions to a partial differential equation accounting for the longitudinal diffusion processes only. Although each diffusion-dispersed sample part is equilibrated between two phases, the resulting σ,D (= 2D mt m + 2D st s) can be interpreted as the sum of two independent contributions in accordance with the variance addition rule. (D m and D s are the mean diffusion coefficients and t mand t s the mean residence times of the sample in the mobile and stationary phases, respectively.) The same σD expression is derived from the random walk model of Giddings by treating the diffusional process in each phase as statistically independent of the other processes. Under these conditions the broadening contribution from longitudinal diffusion in the mobile phase is shown to be independent of the velocity profile. 相似文献
22.
Summary We present a molecular theory of the energy distributions for the internal quantum states of a solute in a liquid or glassy solvent. We show that the energy distributions for different states are correlated in a way that depends on the solute-solvent interactions. We show how the theory can be modified easily to describe the transition-energy distributions for different pairs of states, which are of course related to inhomogeneously broadened absorption spectra. We also show that the distributions for different transitions are correlated, and describe how this correlation is measured by nonresonant fluorescence- and phosphorescence-line-narrowing and hole-burning experiments. The theory provides a microscopic framework within which to interpret different phenomenological models. For the case of a Lennard-Jones solute in a Lennard-Jones liquid solvent, we compare our theory to Monte Carlo simulation. 相似文献
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The peak effect (PE) in the critical current density in both low and high temperature superconductors has been the subject
of a large amount of experimental and theoretical work in the last few/several years. In the case of YBCO, crucial discussions
describing a dynamic or a static picture are not settled. In that region of field and temperature the mobility of the vortex
lattice (VL) is found to be dependent on the dynamical history. Recently we reported evidence that the VL reorganizes and
accesses to robust VL configurations (VLCs) with different effective pinning potential wells arising in response to different
system histories. One of the keys to understand the nature of the PE is to investigate the VL behavior in the vicinity of
the various VLCs in the region of the PE. The stability of these VLCs was investigated and it was found that they have distinct
characteristic relaxation times, which may be related to elastic or plastic creep processes. In this paper we review some
of these results and propose a scenario to describe the PE in YBCO crystals. 相似文献
25.
运用基于第一性原理的密度泛函理论(DFT)的非平衡格林函数(NEGF)方法对Li原子嵌入后的zigzag型单壁碳纳米管(SWCNT)的电子输运性质进行了研究.在构建和优化了Li原子嵌入的zigzag型单壁碳纳米管的电子输运模型后,研究了该系统的电子传输概率、能态密度、电子透射谱,还研究了电子能量和偏置电压设置与变化对其电子输运特性的影响.结果显示zigzag型单壁碳纳米管嵌入Li原子后,电子输运特性发生了较大变化,具有电子输运拓宽效应和量子台阶复苏效应.
关键词:
Li原子
碳纳米管
电子输运
拓宽效应 相似文献
26.
A time domain dispersion measurement apparatus was successfully built and tested at the Indian Institute of Technology, Madras. This instrument can measure directly the pulse broadening in a multimode optical fibre. The basic dispersion mechanisms in optical fibres and the design details of the system are discussed. 相似文献
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T. M. Petrova A. M. Solodov A. A. Solodov V. M. Deichuli V. I. Starikov 《Molecular physics》2018,116(10):1409-1420
The water vapour line broadening and shifting for 97 lines in the ν1 + ν2 + ν3 band induced by hydrogen pressure are measured with Bruker IFS 125 HR FTIR spectrometer. The measurements were performed at room temperature, at the spectral resolution of 0.01 cm?1 and in a wide pressure range of H2. The calculations of the broadening γ and shift δ coefficients were performed in the semi-classical method framework with use of an effective vibrationally depended interaction potential. Two potential parameters were optimised to improve the quality of calculations. Good agreements with measured broadening coefficients were achieved. The comparison of calculated broadening coefficients γ with the previous measurements is discussed. The analytical expressions that reproduce these coefficients for rotational, ν2, ν1, and ν3 vibrational bands are presented. 相似文献