全文获取类型
收费全文 | 93篇 |
免费 | 0篇 |
专业分类
化学 | 37篇 |
晶体学 | 1篇 |
物理学 | 55篇 |
出版年
2018年 | 1篇 |
2017年 | 4篇 |
2016年 | 3篇 |
2015年 | 1篇 |
2013年 | 1篇 |
2012年 | 4篇 |
2011年 | 2篇 |
2010年 | 5篇 |
2009年 | 2篇 |
2008年 | 4篇 |
2007年 | 3篇 |
2006年 | 6篇 |
2005年 | 4篇 |
2004年 | 2篇 |
2002年 | 2篇 |
2001年 | 2篇 |
2000年 | 4篇 |
1999年 | 1篇 |
1997年 | 3篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1994年 | 3篇 |
1993年 | 7篇 |
1992年 | 3篇 |
1991年 | 2篇 |
1990年 | 1篇 |
1989年 | 3篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1983年 | 2篇 |
1978年 | 1篇 |
1977年 | 1篇 |
1976年 | 3篇 |
1975年 | 1篇 |
1974年 | 3篇 |
1973年 | 2篇 |
排序方式: 共有93条查询结果,搜索用时 140 毫秒
11.
12.
Sanchez-Yamagishi JD Taychatanapat T Watanabe K Taniguchi T Yacoby A Jarillo-Herrero P 《Physical review letters》2012,108(7):076601
We investigate electronic transport in dual-gated twisted-bilayer graphene. Despite the subnanometer proximity between the layers, we identify independent contributions to the magnetoresistance from the graphene Landau level spectrum of each layer. We demonstrate that the filling factor of each layer can be independently controlled via the dual gates, which we use to induce Landau level crossings between the layers. By analyzing the gate dependence of the Landau level crossings, we characterize the finite interlayer screening and extract the capacitance between the atomically spaced layers. At zero filling factor, we observe an insulating state at large displacement fields, which can be explained by the presence of counterpropagating edge states with interlayer coupling. 相似文献
13.
Shmuel Cohen Georgia Wollmann Lina Ben-Dor Yizhak Marcus 《Journal of Crystal Growth》2004,270(3-4):589-592
Single crystals of the congruently melting equimolar mixture of magnesium nitrate hexahydrate and nickel nitrate hexahydrate have been grown. The compound crystallizes in a structure foreign to both components, namely in the monoclinic cobalt nitrate hexahydrate structure. The cations are located at random on the cation sub-lattice of the latter crystalline structure. 相似文献
14.
15.
16.
17.
L. Giorgio Soldi Yizhak Marcus Michael J. Blandamer Paul M. Cullis 《Journal of solution chemistry》1995,24(3):201-209
Enthalpic pairwise interaction parameters, hjj, were determined by titration calorimetry at 25°C for dilute solutions of glycerol, D-threitol, manitol, and D-glucitol in water. The parameters for these and other polyols conform to the expression hjj (J-kg–1)=145+135nOH–21.5n
OH
2
–41.7
dl
2
-160.5ndlld, where nOH=nC is the number of hydroxyl groups (carbon atoms), ndl is the number of dl configuration of a vicinal pair of OH-groups, and ndlld is the number of such configurations in the polyol molecules. A rationalization of this expression is given. 相似文献
18.
Yizhak Marcus 《Journal of solution chemistry》2004,33(5):549-559
Standard partial molar volumes of ions were obtained from literature data on 1:1 electrolytes in mixtures of propylene carbonate (PC) with acetonitrile (MeCN) and of water (W) with methanol (MeOH) at 298.15 K. The hypothesis was examined that when the solvents in the mixtures do not differ too much in their polarity and/or hydrogen-bonding ability, only negligible preferential solvation occurs in the solvent shell around the ion where electrostriction takes place. Given the solvent-independent intrinsic volume of an ion, the electrostriction, calculated by the shell-by-shell method, permits the examination of this proposition. This hypothesis was indeed validated by the calculated standard partial molar ionic volumes in the dipolar aprotic mixtures and in the protic aqueous methanol. 相似文献
19.
The solubilities of indomethacin (IMC) in 1,4-dioxane + water cosolvent mixtures were determined at several temperatures, 293.15–313.15 K. The thermodynamic functions: Gibbs energy, enthalpy, and entropy of solution and of mixing were obtained from these data by using the van’t Hoff and Gibbs equations. The solubility was maximal in 0.95 mass fraction of 1,4-dioxane and very low in pure water at all the temperatures. A non-linear plot of ΔHsoln ° vs. ΔGsoln ° with negative slope from pure water up to 0.60 mass fraction of 1,4-dioxane and positive beyond this up to 0.95 mass fraction of 1,4-dioxane was obtained. Accordingly, the driving mechanism for IMC solubility in water-rich mixtures is the entropy, probably due to water-structure loss around the drug non-polar moieties by 1,4-dioxane, whereas, above 0.60 mass fraction of 1,4-dioxane the driving mechanism is the enthalpy, probably due to IMC solvation increase by the co-solvent molecules. The preferential solvation of IMC by the components of the solvent was estimated by means of the quasi-lattice quasi-chemical method, whereas the inverse Kirkwood-Buff integral method could not be applied because of divergence of the integrals in intermediate compositions. 相似文献
20.