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   324篇
  免费   10篇
  国内免费   27篇
化学   147篇
晶体学   1篇
力学   27篇
数学   21篇
物理学   165篇
  2024年   1篇
  2023年   46篇
  2022年   5篇
  2021年   4篇
  2020年   6篇
  2019年   4篇
  2018年   7篇
  2017年   3篇
  2016年   7篇
  2015年   6篇
  2014年   9篇
  2013年   22篇
  2012年   20篇
  2011年   23篇
  2010年   25篇
  2009年   24篇
  2008年   19篇
  2007年   17篇
  2006年   15篇
  2005年   10篇
  2004年   7篇
  2003年   9篇
  2002年   7篇
  2001年   11篇
  2000年   7篇
  1999年   2篇
  1998年   2篇
  1997年   5篇
  1996年   2篇
  1995年   3篇
  1994年   1篇
  1993年   5篇
  1992年   3篇
  1991年   4篇
  1990年   1篇
  1989年   2篇
  1988年   4篇
  1987年   2篇
  1986年   3篇
  1985年   1篇
  1984年   3篇
  1983年   1篇
  1981年   1篇
  1978年   1篇
  1970年   1篇
排序方式: 共有361条查询结果,搜索用时 15 毫秒
11.
Hard carbon is promising anode for potassium-ion batteries(PIBs),however,the poor rate capability hinders its development as potential anode.To address this question,we design a sulfur-doped porous hard carbon(S-HC)for PIBs through the combination of structural design and composition adjustment.The as-designed S-HC exhibits a long cycling life with^191 mAh/g after 300 cycles at 1 A/g,and an excellent rate capability with^100 mAh/g at 5 A/g,which was attributed to its structural characteristics and compositions.The S-HC demonstrates to be promising anode in the future.  相似文献   
12.
本文利用DSC、IR、WAXD、PLM和SALS等实验手段,探讨了具有相同软段的聚酯型脂肪族和芳香族聚氨酯硬段结晶特性的差异,发现脂肪族聚氨酯的相分离速率极快,氢键主要在硬段间形成,因而对硬段的结晶过程影响不大;而芳香族聚氨酯的相分离速率较慢,软硬段间又能形成氢键,因而对硬段的结晶起了阻碍作用。  相似文献   
13.
合成了一系列不同分子量的聚己内酯,进而制备异氰酸根封端的聚己内酯预聚体,用傅里叶变换红外光谱研究了不同分子量的聚己内酯预聚体与二元醇的扩链反应.扩链反应动力学研究结果表明:聚己内酯预聚体与二元醇的扩链反应均为二级反应;随着软链段反应物料分子量的增加,反应速率常数显著降低,但当分子量超过某一范围后,其对反应速率的影响逐渐减小,趋于不变.对于不同硬链段反应物料含量的扩链反应体系,硬链段反应物料含量越高,软链段反应物料分子量对反应速率的影响越明显,而且,当软链段反应物料分子量超过某一范围后,不同体系的反应速率常数间的差值趋于不变.Arrhenius方程中的指前因子(B)随软链段反应物料分子量的变化关系与速率常数对分子量的依赖关系相同;从反应速率常数对温度的依赖关系可见:表观活化能的直线斜率基本相同,扩链反应的活化能主要与官能团的反应活性相关.  相似文献   
14.
The mesoporous carbon material with large pore volume and high surface area by a simple situ MgO template method is synthesized, which is utilized as cathode to assemble a high performance lithium ion capacitor.  相似文献   
15.
本文对近十年红外光谱在定量分析中的应用进行了概述。偏最小二乘法,一阶导数、二阶导数等化学计量法在定量分析中得到了普遍的应用,反射、探针、漫反射等技术的发展拓宽了红外光谱定量分析的领域。固体、液体、气体均可计量的优势更加突出。实现了单一物质,二元或多元物质的定量测定。  相似文献   
16.
We have observed magnetic anisotropy in bulk Nd55−xCoxFe30Al10B5 (x=10, 15 and 20) alloys prepared by copper mold suction casting method with a presence of external magnetic field (quenching field) μ0H=0.25 T. By changing direction of the measuring field from perpendicular to parallel one in comparison with that of the quenching field, coercive force of the alloys slightly decreases while remanent magnetization and squareness of hysteresis loop increase more clearly. It is also found that the higher Co-concentration in the alloys the larger magnetic anisotropy is induced. The structure analyses manifest nanocrystalline particles embedded in residual amorphous matrix of the alloys. The size of the particles is in range of 10-30 nm and their crystalline phases consist of Nd2(Fe,Co)14B, Nd3Co, Nd3Al, NdAl2 and Nd.  相似文献   
17.
Building on a recent paper [8], here we argue that the combinatorics of matroids are intimately related to the geometry and topology of toric hyperkähler varieties. We show that just like toric varieties occupy a central role in Stanley’s proof for the necessity of McMullen’s conjecture (or g-inequalities) about the classification of face vectors of simplicial polytopes, the topology of toric hyperkähler varieties leads to new restrictions on face vectors of matroid complexes. Namely in this paper we will give two proofs that the injectivity part of the Hard Lefschetz theorem survives for toric hyperkähler varieties. We explain how this implies the g-inequalities for rationally representable matroids. We show how the geometrical intuition in the first proof, coupled with results of Chari [3], leads to a proof of the g-inequalities for general matroid complexes, which is a recent result of Swartz [20]. The geometrical idea in the second proof will show that a pure O-sequence should satisfy the g-inequalities, thus showing that our result is in fact a consequence of a long-standing conjecture of Stanley.  相似文献   
18.
In this study ground and excited states acidic dissociation constants of a recently synthesized Schiff base was obtained in a DMF:water mixture of 30:70 (v/v) using absorption and fluorescent spectra of the Schiff base in different pH values with the aid of chemometric methods. In addition, the fluorescent of the two kinds of tautomers of this Schiff base was investigated and the rate of tautomerization was obtained using rank annihilation factor analysis (RAFA). The effect of different kinds of surfactants such as sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB) and Triton X-100 on fluorescence spectrum of the Schiff base in a DMF:water mixture of 2:98 (v/v) was investigated. CTAB increased the fluorescence intensity of the Schiff base while SDS and Triton X-100 had no significant effect on it. β-Cyclodextrin increased the fluorescence intensity of the Schiff base. Also the sensing behavior of this Schiff base toward metal ions was studied in DMF and ethanol by fluorescence spectroscopy. The Schiff base showed prominent fluorescent signal in the presence of Zn2+, whereas other metal ions failed to induce response and ground-state dissociation constant of the complex was determined by direct fluorimetric titration as a function of Zn2+ concentration.  相似文献   
19.

Combined theoretical and experimental investigations led to the discovery of a new polymorph of titanium dioxide with titanium nine-coordinated to oxygen in the cotunnite (PbCl 2 ) structure. Hardness measurements on the cotunnite-structured TiO 2 synthesized at pressures above 60 GPa and temperatures above 1000 K reveal that this material is the hardest oxide yet discovered. Furthermore, it is one of the least compressible (with a measured bulk modulus of 431 GPa) and hardest (with a microhardness of 38 GPa) polycrystalline materials studied thus far.  相似文献   
20.
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