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   559篇
  免费   15篇
  国内免费   6篇
化学   261篇
晶体学   3篇
力学   8篇
数学   188篇
物理学   120篇
  2023年   5篇
  2022年   5篇
  2021年   3篇
  2020年   10篇
  2019年   11篇
  2018年   7篇
  2017年   4篇
  2016年   14篇
  2015年   13篇
  2014年   24篇
  2013年   24篇
  2012年   25篇
  2011年   36篇
  2010年   18篇
  2009年   21篇
  2008年   25篇
  2007年   22篇
  2006年   33篇
  2005年   27篇
  2004年   24篇
  2003年   19篇
  2002年   17篇
  2001年   23篇
  2000年   13篇
  1999年   10篇
  1998年   7篇
  1997年   6篇
  1996年   7篇
  1995年   9篇
  1994年   9篇
  1993年   6篇
  1992年   12篇
  1991年   9篇
  1990年   9篇
  1989年   5篇
  1988年   4篇
  1987年   3篇
  1985年   5篇
  1984年   8篇
  1983年   7篇
  1982年   4篇
  1981年   5篇
  1980年   5篇
  1979年   6篇
  1977年   4篇
  1976年   2篇
  1975年   3篇
  1973年   2篇
  1970年   2篇
  1968年   2篇
排序方式: 共有580条查询结果,搜索用时 31 毫秒
571.
We have studied the differential capacitance of self-assembly hybrid organic/inorganic quantum dot (QD) light-emitting devices (QD-OLEDs) at room temperature in the frequency range of 1×103 to 1×106 Hz. Self-assembly CdSe/ZnS QDs monolayer was used to fabricate trilayer hybrid QD-OLEDs on indium tin oxide coated glass substrates. We observed negative differential capacitance (NDC) in both OLED and QD-OLEDs for the first time in the intermediate frequency range of 5×103 to 5×105 Hz. The onset and frequency range of NDC are strongly depended on the applied bias voltage. This behavior is described by a mathematical model. The simulated results showed that the NDC was due to the time-dependent transient current from the QDs and organic/metal interfacial states in the device. The probable mechanisms of NDC in organic devices are discussed.  相似文献   
572.
In this paper, we consider a class of optimal control problems subject to equality terminal state constraints and continuous state and control inequality constraints. By using the control parametrization technique and a time scaling transformation, the constrained optimal control problem is approximated by a sequence of optimal parameter selection problems with equality terminal state constraints and continuous state inequality constraints. Each of these constrained optimal parameter selection problems can be regarded as an optimization problem subject to equality constraints and continuous inequality constraints. On this basis, an exact penalty function method is used to devise a computational method to solve these optimization problems with equality constraints and continuous inequality constraints. The main idea is to augment the exact penalty function constructed from the equality constraints and continuous inequality constraints to the objective function, forming a new one. This gives rise to a sequence of unconstrained optimization problems. It is shown that, for sufficiently large penalty parameter value, any local minimizer of the unconstrained optimization problem is a local minimizer of the optimization problem with equality constraints and continuous inequality constraints. The convergent properties of the optimal parameter selection problems with equality constraints and continuous inequality constraints to the original optimal control problem are also discussed. For illustration, three examples are solved showing the effectiveness and applicability of the approach proposed.  相似文献   
573.
574.
575.
The preferential oxidation (PROX) of CO in the presence of H(2) is an important step in the production of pure H(2) for industrial applications. In this report, two sonochemical methods (S1 and S2) were used to prepare highly dispersed Ru catalysts supported on mesoporous TiO(2) (TiO(2)(MSP)) for the PROX reaction, in which a reaction gas mixture containing 1% CO + 1% O(2) + 18% CO(2) + 78% H(2) was used. The supported Ru catalysts performed better than the supported Au and Pt catalysts, and the S1 and S2 methods are superior to the impregnation method. The Ru/TiO(2)(MSP) catalysts were active for the PROX reaction below 200 °C and good for the methanation reactions of CO and CO(2) above 200 °C. The presence of residual chlorine in the catalysts severely suppressed their PROX reaction activity, and a higher dispersion of Ru particles led to better catalytic performances. The addition of Au in the Ru/TiO(2)(MSP) catalyst also caused a poorer catalytic activity for both the PROX and the methanation reactions. TPR results showed that in the active catalysts prepared by the S1 and S2 methods, the well dispersed Ru particles, after calcination in air, had a stronger interaction with the support than those in the catalyst prepared by the impregnation method and in the Au-Ru/TiO(2)(MSP) catalyst. In situ CO absorption experiments performed with the diffusion reflectance Fourier transform infra red (DRIFT) method showed that the bridged adsorbed CO species on isolated Ru(0) sites correlated with the catalytic performances, indicating that these isolated Ru(0) sites are the most active sites of the Ru/TiO(2)(MSP) catalysts in the PROX reaction.  相似文献   
576.
The sonochemical oil-in-water miniemulsion polymerization of n-butyl methacrylate (BMA) has been studied in mixtures with a range of aliphatic and aromatic hydrocarbon liquids under ambient conditions. Measurements of monomer conversion percentage and molecular weights of the BMA polymers were performed to investigate the effect of the various organic liquids on the kinetics of the polymerization process and on the properties of the resultant polymers. Both the rates of polymerization and the molecular weights of the polymers formed were found to be dependent on the amount and type of the organic liquid present in the emulsion. The experimental results revealed that when the organic liquids were aliphatic, there were no significant changes in the rates of BMA polymerization whereas when the organic liquids were aromatic, the rates of polymerization were greatly reduced. Molecular weight data of the BMA polymers showed that in the presence of an organic liquid, the size of the polymer significantly decreased. The results have been interpreted in terms of the formation of a radical complex between the propagating radical and the organic liquid in the oil mixture, as well as chain transfer reactions that affect the kinetics of the polymerization process.  相似文献   
577.
578.
579.
580.
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