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   32641篇
  免费   5788篇
  国内免费   5711篇
化学   17141篇
晶体学   480篇
力学   1084篇
综合类   483篇
数学   2323篇
物理学   9069篇
无线电   13560篇
  2024年   164篇
  2023年   690篇
  2022年   1187篇
  2021年   1294篇
  2020年   1203篇
  2019年   1119篇
  2018年   1106篇
  2017年   1241篇
  2016年   1372篇
  2015年   1764篇
  2014年   2039篇
  2013年   2591篇
  2012年   2976篇
  2011年   3027篇
  2010年   2574篇
  2009年   2551篇
  2008年   2649篇
  2007年   2462篇
  2006年   2306篇
  2005年   1874篇
  2004年   1393篇
  2003年   1058篇
  2002年   1056篇
  2001年   1000篇
  2000年   894篇
  1999年   583篇
  1998年   339篇
  1997年   244篇
  1996年   214篇
  1995年   200篇
  1994年   168篇
  1993年   158篇
  1992年   111篇
  1991年   90篇
  1990年   60篇
  1989年   77篇
  1988年   55篇
  1987年   49篇
  1986年   51篇
  1985年   29篇
  1984年   18篇
  1983年   21篇
  1982年   19篇
  1981年   20篇
  1980年   9篇
  1979年   9篇
  1978年   5篇
  1977年   4篇
  1976年   5篇
  1957年   4篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
11.
JPC – Journal of Planar Chromatography – Modern TLC - A new high-performance thin-layer chromatographic (HPTLC) method has been developed for the simultaneous estimation of...  相似文献   
12.
Let R be a Noetherian unique factorization domain such that 2 and 3 are units,and let A=R[α]be a quartic extension over R by adding a rootαof an irreducible quartic polynomial p(z)=z4+az2+bz+c over R.We will compute explicitly the integral closure of A in its fraction field,which is based on a proper factorization of the coefficients and the algebraic invariants of p(z).In fact,we get the factorization by resolving the singularities of a plane curve defined by z4+a(x)z2+b(x)z+c(x)=0.The integral closure is expressed as a syzygy module and the syzygy equations are given explicitly.We compute also the ramifications of the integral closure over R.  相似文献   
13.
Unreliable mobility values, and particularly greatly overestimated values and severely distorted temperature dependences, have recently hampered the development of the organic transistor field. Given that organic field‐effect transistors (OFETs) have been routinely used to evaluate mobility, precise parameter extraction using the electrical properties of OFETs is thus of primary importance. This review examines the origins of the various mobilities that must be determined for OFET applications, the relevant extraction methods, and the data selection limitations, which help in avoiding conceptual errors during mobility extraction. For increased precision, the review also discusses device fabrication considerations, calibration of both the specific gate‐dielectric capacitance and the threshold voltage, the contact effects, and the bias and temperature dependences, which must actually be handled with great care but have mostly been overlooked to date. This review serves as a systematic overview of the OFET mobility extraction process to ensure high precision and will also aid in improving future research.  相似文献   
14.
15.
For the orthosymplectic Lie superalgebra ◂⋅▸OSP(2,2), we choose a set of basis matrices. A linear combination of those basis matrices presents a spatial spectral matrix. The compatible condition of the spatial part and the corresponding temporal parts of the spectral problem leads to a generalized super AKNS (GSAKNS) hierarchy. By making use of the supertrace identity, the obtained GSAKNS hierarchy can be written as the super bi-Hamiltonian structures.  相似文献   
16.
Covalent organic frameworks (COFs) are a new class of crystalline porous polymers comprised mainly of carbon atoms, and are versatile for the integration of heteroatoms such as B, O, and N into the skeletons. The designable structure and abundant composition render COFs useful as precursors for heteroatom-doped porous carbons for energy storage and conversion. Herein, we describe a multifunctional electrochemical catalyst obtained through pyrolysis of a bimetallic COF. The catalyst possesses hierarchical pores and abundant iron and cobalt nanoparticles embedded with standing carbon layers. By integrating these features, the catalyst exhibits excellent electrochemical catalytic activity in the oxygen reduction reaction (ORR), with a 50 mV positive half-wave potential, a higher limited diffusion current density, and a much smaller Tafel slope than a Pt-C catalyst. Moreover, the catalyst displays superior electrochemical performance toward the hydrogen evolution reaction (HER), with overpotentials of −0.26 V and −0.33 V in acidic and alkaline aqueous solution, respectively, at a current density of 10 mA cm−2. The overpotential in the catalysis of the oxygen evolution reaction (OER) was 1.59 V at the same current density.  相似文献   
17.
18.
通过问卷方式对高职学生信息技术能力进行调查,统计数据,从信息获取、评价、处理、交流能力以及信息道德方面对高职学生信息技术能力特点进行分析。  相似文献   
19.
Naphthalimide‐phthalimide derivatives (NDPDs) have been synthesized and combined with an iodonium salt, N‐vinylcarbazole, amine or 2,4,6‐tris(trichloromethyl)‐1,3,5‐triazine to produce reactive species (i.e., radicals and cations). These generated reactive species are capable of initiating the cationic polymerization of epoxides and/or the radical polymerization of acrylates upon exposure to very soft polychromatic visible lights or blue lights. Compared with the well‐known camphorquinone based systems used as references, the novel NDPD based combinations employed here demonstrate clearly higher efficiencies for the cationic polymerization of epoxides under air as well as the radical polymerization of acrylates. Remarkably, one of the NDPDs (i.e., NDPD2) based systems is characterized by an outstanding reactivity. The structure/reactivity/efficiency relationships of the investigated NDPDs were studied by fluorescence, cyclic voltammetry, laser flash photolysis, electron spin resonance spin trapping, and steady state photolysis techniques. The key parameters for their reactivity are provided. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 665–674  相似文献   
20.
全媒体技术的发展推动我们进入全媒体时代,在全媒体时代下,综艺晚会要以引领大众的审美潮流以及与观众保持较强的互动作为发展方向。总结了全媒体时代下综艺晚会的有效发展策略,包括精心策划、利用高科技等。  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