首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   5403篇
  免费   496篇
  国内免费   617篇
化学   2578篇
晶体学   20篇
力学   379篇
综合类   104篇
数学   2743篇
物理学   692篇
  2024年   14篇
  2023年   70篇
  2022年   93篇
  2021年   95篇
  2020年   145篇
  2019年   158篇
  2018年   132篇
  2017年   184篇
  2016年   181篇
  2015年   156篇
  2014年   230篇
  2013年   386篇
  2012年   355篇
  2011年   288篇
  2010年   269篇
  2009年   310篇
  2008年   381篇
  2007年   363篇
  2006年   335篇
  2005年   308篇
  2004年   280篇
  2003年   236篇
  2002年   213篇
  2001年   190篇
  2000年   145篇
  1999年   149篇
  1998年   136篇
  1997年   106篇
  1996年   102篇
  1995年   82篇
  1994年   85篇
  1993年   66篇
  1992年   45篇
  1991年   52篇
  1990年   28篇
  1989年   18篇
  1988年   13篇
  1987年   16篇
  1986年   10篇
  1985年   17篇
  1984年   16篇
  1983年   12篇
  1982年   13篇
  1981年   11篇
  1980年   2篇
  1979年   5篇
  1978年   4篇
  1974年   3篇
  1973年   2篇
  1936年   3篇
排序方式: 共有6516条查询结果,搜索用时 31 毫秒
1.
2.
In this article, we construct and analyze a residual-based a posteriori error estimator for a quadratic finite volume method (FVM) for solving nonlinear elliptic partial differential equations with homogeneous Dirichlet boundary conditions. We shall prove that the a posteriori error estimator yields the global upper and local lower bounds for the norm error of the FVM. So that the a posteriori error estimator is equivalent to the true error in a certain sense. Numerical experiments are performed to illustrate the theoretical results.  相似文献   
3.
4.
The mechanism of lithium insertion that occurs in an iron oxyfluoride sample with a hexagonal–tungsten–bronze (HTB)-type structure was investigated by the pair distribution function. This study reveals that upon lithiation, the HTB framework collapses to yield disordered rutile and rock salt phases followed by a conversion reaction of the fluoride phase toward lithium fluoride and nanometer-sized metallic iron. The occurrence of anionic vacancies in the pristine framework was shown to strongly impact the electrochemical activity, that is, the reversible capacity scales with the content of anionic vacancies. Similar to FeOF-type electrodes, upon de-lithiation, a disordered rutile phase forms, showing that the anionic chemistry dictates the atomic arrangement of the re-oxidized phase. Finally, it was shown that the nanoscaling and structural rearrangement induced by the conversion reaction allow the in situ formation of new electrode materials with enhanced electrochemical properties.  相似文献   
5.
Over the last 20 years a large number of algorithms has been published to improve the speed and domain of convergence of continued fractions. In this survey we show that these algorithms are strongly related. Actually, they essentially boil down to two main principles.We also prove some results on asymptotic expansions of tail values of limit periodic continued fractions.Dedicated to Luigi Gatteschi on his seventieth birthdayThis research was partially supported by The Norwegian Research Council and by the HMC project ROLLS, under contract CHRX-CT93-0416.  相似文献   
6.
In this paper, the authors studied certain properties of the estimate of Liang and Krishnaiah (1985, J. Multivariate Anal. 16, 162–172) for multivariate binary density. An alternative shrinkage estimate is also obtained. The above results are generalized to general orthonormal systems.  相似文献   
7.
关于AOR迭代法的研究   总被引:5,自引:0,他引:5  
本文论证了严格对角占优矩阵之AOR法的误差估计式中的误差估计常数hγ,ω(0≤γ≤ω0)的最小值是h1,1.  相似文献   
8.
Modified three-dimensional formulations of bending problems of homogeneous elastic plates and beams are considered. Modification of the known three-dimensional formulations reduces to using additional constraints imposed on displacement functions. An advantage of the formulations proposed is that complex fixing conditions of plates and beams can be taken into account.  相似文献   
9.
Yanmao Shi  Ping Wu  Pan Du  Chenxin Cai 《Acta Physico》2006,22(10):1227-1233
A new electroactive polynuclear inorganic compound of rare earth metal, gadolinium hexacyanoferrate (GdHCF), was prepared and characterized using the techniques of FTIR spectroscopy, thermogravimetric analysis (TG), UV-Vis spectrometry, X-ray photoelectron spectroscopy (XPS), ICP atomic emission spectroscopy, and EDX. The results of ICP atomic emission spectroscopy, EDX, and TGA indicated that the prepared GdHCF sample had a stoichiometry of NaGdFe(CN)6·12H2O (when GdHCF was prepared in NaCl solution). The FTIR spectrum of GdHCF showed that there were two types of water molecules in the structure of GdHCF: one was the interstitial water (5 H2O), which resulted from the association of water due to H-bonding, and the other was water coordinated with Gd (7 H2O). The results obtained using XPS showed that the oxidation state of Fe and Gd in the GdHCF sample was +2 and +3, respectively. GdHCF was immobilized on the surface of spectroscopically pure graphite (SG) electrode forming the GdHCF/SG electrode, and the solid-state electrochemistry of the resultant electrode was studied using cyclic voltammetry. The cyclic voltammetric results indicated that the GdHCF/SG electrode exhibited a pair of well-defined and stable redox peaks with the formal potential of E0′=(197±3) mV. The effects of the concentration of the supporting electrolyte on the electrochemical characteristics of GdHCF were studied, and the results showed that the value of E0′ increased linearly with the activity of the cationic ion of the supporting electrolyte (lgaNa+), with a slope of 54.1 mV, which may become a novel method for determining the activity of Na+ in solution. Further experimental results indicated that GdHCF had electrocatalytic activities toward the oxidation of dopamine (DA) and ascorbic acid (AA), and the electrocatalytic current increased linearly with the concentration of DA (or AA) in the range of 1.0–10.0 mmol·L?1 (for DA) or 0.5–20.0 mmol·L?1 (for AA).  相似文献   
10.
王建力 《数学杂志》2003,23(3):285-289
摘要:本文在L_[0.1]~p空间给出了 Durrmeyer型修正的shepard算子D_n(f,x),对 f∈L_[0.1]~p,(p≥1),得到了下列的Jackson型估计:││D)n(f)-f││_p≤ C_(pλω)(f,n~(-1))p,λ≥2, Cω(f,n~(-1)logn)p,λ=2, C_(pλω)(f,n~(-1))p,1<λ<2,  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号