全文获取类型
收费全文 | 4220篇 |
免费 | 873篇 |
国内免费 | 896篇 |
专业分类
化学 | 3804篇 |
晶体学 | 72篇 |
力学 | 46篇 |
综合类 | 54篇 |
数学 | 321篇 |
物理学 | 1692篇 |
出版年
2024年 | 13篇 |
2023年 | 53篇 |
2022年 | 112篇 |
2021年 | 141篇 |
2020年 | 165篇 |
2019年 | 146篇 |
2018年 | 138篇 |
2017年 | 122篇 |
2016年 | 191篇 |
2015年 | 184篇 |
2014年 | 235篇 |
2013年 | 396篇 |
2012年 | 309篇 |
2011年 | 289篇 |
2010年 | 257篇 |
2009年 | 281篇 |
2008年 | 295篇 |
2007年 | 288篇 |
2006年 | 295篇 |
2005年 | 252篇 |
2004年 | 265篇 |
2003年 | 221篇 |
2002年 | 142篇 |
2001年 | 127篇 |
2000年 | 150篇 |
1999年 | 124篇 |
1998年 | 111篇 |
1997年 | 92篇 |
1996年 | 85篇 |
1995年 | 85篇 |
1994年 | 78篇 |
1993年 | 51篇 |
1992年 | 57篇 |
1991年 | 60篇 |
1990年 | 30篇 |
1989年 | 29篇 |
1988年 | 21篇 |
1987年 | 12篇 |
1986年 | 11篇 |
1985年 | 15篇 |
1984年 | 10篇 |
1983年 | 7篇 |
1982年 | 14篇 |
1981年 | 8篇 |
1980年 | 2篇 |
1979年 | 9篇 |
1978年 | 5篇 |
1973年 | 2篇 |
1972年 | 1篇 |
1971年 | 1篇 |
排序方式: 共有5989条查询结果,搜索用时 31 毫秒
31.
R. Venkat narayan Vinod Kanniah Aruna Dhathathreyan 《Journal of Chemical Sciences》2006,118(2):179-184
Cobalt oxides were prepared by three different methods: (1) by reacting cobalt nitrate with oxalic acid, (2) co-precipitating
cobalt nitrate with sodium carbonate, and (3) using sodium dodecyl sulphate as organic surfactant. All three samples were
characterized before and after calcination by solvent extraction and the resulting products examined by IR spectroscopy. In
the case of method 3, the removal of surfactant was followed by TGA studies. Products from all three methods were identified
by XRD. Peaks in low angle XRD indicate the porous nature of the oxides. The morphology of the pores was studied by transmission
electron microscopy. Some irregular pore structures were obtained for samples from methods 1 and 2, with an average size of
4–6 nm. Only the product from method 3 using SDS as template showed ordered structure and optimum size, and Brunauer-Emmet-Teller
surface areas of the as-prepared, as well as the treated samples, exhibited H3 type hysteresis. The samples from the three
methods were used as catalysts in the oxidation reaction of cyclohexane under mild conditions and the catalytic efficiency
of the cobalt oxide was comparable with mesoporous cobalt oxides. 相似文献
32.
Jing Yang 《Applied Surface Science》2006,253(4):1988-1994
To use solar irradiation or interior lighting efficiently, we sought a photocatalyst with high reactivity under visible light. Nitrogen and carbon doping TiO2−x−yNxCy films were obtained by heating the TiO2 gel in an ionized N2 gas and then were calcined at 500 °C. The TiO2−x−yNxCy films have revealed an improvement over the TiO2 films under visible light (wavelength, 500 nm) in optical absorption and photocatalytic activity such as photodegradation of methyl orange. X-ray photoemission spectroscopy, infrared spectrum and UV-visible (UV-vis) spectroscopy were used to find the difference of two kinds of films. Nitrogen and carbon doped into substitutional sites of TiO2 has been proven to be indispensable for band-gap narrowing and photocatalytic activity. 相似文献
33.
The reaction system (NH4)3VS4/CuCl/PPh3/Et4NBr afforded a series of [VS4-Cun] dusters with various core configurations in the solid state at low heating temperature. The structural regularity of [VS4-Cun] dusters and the influence of the CuCl:(NH4)3VS4 ratio as well as that of reaction temperature and time on the formation of duster core have been summarized. The reaction mechanism of forming V-Cu-S clusters has also been explored. 相似文献
34.
We investigate the topology of the phase diagram of binary alloys on the fee lattice with first-neighbor antiferromagnetic interactions around the superdegenerate point, where the L10 and L12 phases meet. We treat the system as a hard-constraint lattice gas, following a procedure previously described by Lebowitzet al. We perform cluster variation method calculations in theT0 limit and Monte Carlo simulations directly atT=0 K on the ground states of the superdegenerate point. We find that: (i) there is no disordered phase in the neighborhood of this point; (ii) a phase L for which two of the four cubic sublattices have the same average occupancy and each of the two others are different appears between L10 and L12; (iii) the transition L/L12 is of first order. 相似文献
35.
Considering a system ofN identical interacting particles, which obey Fermi-Dirac or Bose-Einstein statistics, we derive new formulas for correlation functions of the type
(whereB
j is diagonal in the free-particle states) in the thermodynamic limit. Thereby we apply and extend a superoperator formalism, recently developed for the derivation of long-time tails in semiclassical systems. As an illustrative application, the Boltzmann equation value of the time-integrated correlation functionC(t) is derived in a straightforward manner. Due to exchange effects, the obtained t-matrix and the resulting scattering cross section, which occurs in the Boltzmann collision operator, are now functionals of the Fermi-Dirac or Bose-Einstein distribution. 相似文献
36.
负载型双金属簇催化剂的多相一氧化碳加氢反应性能索全伶,李晔(内蒙古工业大学化学工程系,呼和浩特010062)殷元骐,金道森(中国科学院兰州化学物理研究所,兰州730000)关键词一氧化碳加氢,多相催化,双金属簇催化剂,钾效应。1.引言异核金属羰基簇作... 相似文献
37.
Three novel hetero-polyoxovanadates, [Cd(2,2′-bpy)3]{[Cd(dien)]As8V14O42(H2O)} (1, 2,2′-bpy=2,2′-bipyridine, and dien=diethylenetriamine), [Zn(2,2′-bpy)2]2[As8V14O42(H2O)]·H2O (2) and [Ni(en)2]3[As8V14O42(HPO3)]·4H2O (3, en=ethlenediamine), were hydrothermally synthesized and characterized by single-crystal X-ray diffraction. Crystal data: 1 monoclinic, P2(1)/n, a=15.1728(5), b=19.2863(5), , β=96.005(2)°, Z=4. 2, orthorhombic, P2(1)2(1)2(1), a=12.1270(3), b=15.8678(8), , Z=4. 3, triclinic, , a=12.9340(3), b=13.4130(3), , α=87.170(3)°, β=77.517(3)°, γ=68.480(3)°, Z=2. Compounds 1-3 are all made of the {As8V14O42} shells linked by corresponding transition metal complexes into extended structures. Compound 1 and 2 present 1-D wave-like and tubular structures, respectively, while compound 3 exhibits a novel 2-D structure containing interwinding puckery layers. Variable temperature susceptibility measurements demonstrate the presence of antiferromagnetic interaction between VIV cations in 1 and 2. 相似文献
38.
39.