全文获取类型
收费全文 | 1963篇 |
免费 | 63篇 |
国内免费 | 214篇 |
专业分类
化学 | 1878篇 |
晶体学 | 37篇 |
力学 | 25篇 |
综合类 | 5篇 |
数学 | 2篇 |
物理学 | 293篇 |
出版年
2024年 | 3篇 |
2023年 | 44篇 |
2022年 | 24篇 |
2021年 | 48篇 |
2020年 | 60篇 |
2019年 | 34篇 |
2018年 | 36篇 |
2017年 | 33篇 |
2016年 | 43篇 |
2015年 | 52篇 |
2014年 | 64篇 |
2013年 | 90篇 |
2012年 | 200篇 |
2011年 | 105篇 |
2010年 | 82篇 |
2009年 | 129篇 |
2008年 | 117篇 |
2007年 | 132篇 |
2006年 | 103篇 |
2005年 | 92篇 |
2004年 | 93篇 |
2003年 | 85篇 |
2002年 | 62篇 |
2001年 | 56篇 |
2000年 | 65篇 |
1999年 | 62篇 |
1998年 | 57篇 |
1997年 | 39篇 |
1996年 | 36篇 |
1995年 | 34篇 |
1994年 | 37篇 |
1993年 | 27篇 |
1992年 | 18篇 |
1991年 | 24篇 |
1990年 | 15篇 |
1989年 | 11篇 |
1988年 | 7篇 |
1987年 | 4篇 |
1986年 | 4篇 |
1985年 | 4篇 |
1984年 | 5篇 |
1980年 | 2篇 |
1979年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有2240条查询结果,搜索用时 15 毫秒
1.
Vsevolod Khikhlovskyi Albert J. J. M. van Breemen Jasper J. Michels René A. J. Janssen Gerwin H. Gelinck Martijn Kemerink 《Journal of Polymer Science.Polymer Physics》2015,53(17):1231-1237
In many organic electronic devices functionality is achieved by blending two or more materials, typically polymers or molecules, with distinctly different optical or electrical properties in a single film. The local scale morphology of such blends is vital for the device performance. Here, a simple approach to study the full 3D morphology of phase‐separated blends, taking advantage of the possibility to selectively dissolve the different components is introduced. This method is applied in combination with AFM to investigate a blend of a semiconducting and ferroelectric polymer typically used as active layer in organic ferroelectric resistive switches. It is found that the blend consists of a ferroelectric matrix with three types of embedded semiconductor domains and a thin wetting layer at the bottom electrode. Statistical analysis of the obtained images excludes the presence of a fourth type of domains. The criteria for the applicability of the presented technique are discussed. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1231–1237 相似文献
2.
Marcelino Maneiro Manuel R. Bermejo M. Isabel Fernndez Ana M. Gonzlez‐Noya Alexei M. Tyryshkin Robin G. Pritchard 《无机化学与普通化学杂志》2003,629(2):285-290
A new MnIII‐Schiff base complex, [MnL(OH2)](ClO4) ( 1 ) (H2L = N, N′‐bis‐(3‐Br‐5‐Cl‐salicylidene)‐1, 2‐diimino‐2‐methylethane), an inorganic model of the catalytic center (OEC, Oxygen Evolving Complex) in photosystem II (PSII), has been synthesized and characterized by elemental analysis, IR and EPR spectroscopy, mass spectrometry, magnetic susceptibility measurement and the study of its redox properties by cyclic and normal pulse voltammetry. This complex mimics reactivity (showing a relevant photolytic activity), and also some structural characteristics (parallel‐mode MnIII EPR signal from partially assembled OEC cluster) of the natural OEC. The complex 1 was found to rearrange in solution into a crystallographically solved square‐pyramidal complex, [MnLL′] ( 2 ) (HL′ = 6‐bromo‐4‐chloro‐2‐cyanophenol), through a process, which probably liberates radical species (detected by EPR), and provokes a C—N bond cleavage in the ligand. A photo‐radical mechanism is discussed to explain this rearrangement. 相似文献
3.
Thermal behaviour and biochemical activity of potassium-silicate-phosphate glasses modified by addition of Ca, Mg, acting
as ecological fertilisers of controlled release rate of the nutrients for plants were studied. It has been found that the
biochemical activity of silicate-phosphate glasses depends on the nature and the number of components forming the glassy framework
and is related to the thermal stability of glass demonstrated by the formation of new compounds during the process of crystallisation.
It is proved that these seemingly different properties are determined by the same parameters which are the strengths bonds
of glass network-formers and modifiers as well as their chemical affinity.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
4.
The 2D Rancieite type manganic acid was prepared by reduction of KMnO4 in acidic medium. Its ion exchange behavior allows to prepare alkali derivatives. All compounds were characterized with use of a combination of X-ray diffraction, chemical analyses, TGA, magnetic measurements and spectroscopic techniques. The evolution of their chemical composition versus temperature was studied between 180 and 400 °C. It shows that the dehydration process is partly reversible in these compounds whereas the weak reduction is irreversible. The 2D Rancieite-type manganic acid is readily different from a Birnessite-type phyllomanganate, as shown by several features: the interlayer distance, the ion exchange capacity, the thermal behavior, the interlayer cation content, the manganese average oxidation state, the magnetic behavior and the IR spectrum. 相似文献
5.
锰结核中硅,铝,铁,镁,磷,钾,锰,钛的XRFA 总被引:1,自引:0,他引:1
本文叙述了用XRF分析锰结核中Si、Al、Fe、Mg、P、K、Mn和Ti的方法。按照通常锰结核的主次成分制备6个人工合成标准,根据Sherman方程计算了已知成分(二元系统)的相对强度。用L-T方求得了互致元素校正的理论α系数(基本的、混合的、修正的),用DATAFLEX151B计算机以BASIC语言汇了“PRA,APU”计算机程序。然后进行非线性回归分析了锰结核样品得到了满意的结果。 相似文献
6.
ICP-AES测定饮用水源中的Cu、Mn、Pb、Cd、Zn 总被引:7,自引:2,他引:5
用ICP-AES法同时测定饮用水源中的Cu、Mn、Pb、Cd、Zn等重金属元素,具有基体效应小、测量范围宽等优点。检出限为0.2-4.0μg/L,回收率为91.5%-103.9%,相对标准偏差为0.29%-1.5%,测定密码样与实际样品,结果令人满意。 相似文献
7.
A. M. Yakunin A. Yu. Silov P. M. Koenraad W. Van Roy J. De Boeck J. H. Wolter 《Superlattices and Microstructures》2003,34(3-6):539
An individual Mn acceptor in GaAs is mapped by cross-sectional scanning tunneling microscopy (X-STM) at room temperature and a strongly anisotropic shape of the acceptor state is observed. An acceptor state manifests itself as a cross-like feature which we attribute to a valence hole weakly bound to the Mn ion forming the (Mn2+3d5+hole) complex. We propose that the observed anisotropy of the Mn acceptor wavefunction is due to the d-wave present in the acceptor ground state. 相似文献
8.
Charlotte Doussier Philippe Léone Alain Meerschaut 《Journal of solid state chemistry》2007,180(8):2323-2334
The new oxy-chloro-sulfide (Mn1−xPbx)Pb10+ySb12−yS26−yCl4+yO (x ∈ [0.2-0.3]; y ∈ [0.3-1.6]) was synthesized by dry way at 500-600 °C. A single crystal ∼Mn0.7Pb11.0Sb11.3S25.3Cl4.7O indicates a monoclinic symmetry, space group C2/m, with a = 37.480(8), b = 4.1178(8), c = 18.167(4) Å, β = 106.37(3)°, V = 2690.2(9) Å3, Z = 2. Its crystal structure was determined by X-ray single crystal diffraction, with a final R = 5.11%. Modular analysis of the crystal structure reveals a “waffle” architecture, where complex rods with lozenge section delimitate an internal channel filled by a single chain of (Mn0.7Pb0.3)Cl6 octahedra connected by opposite edges. Minimal inter-chain distances are close to 18 Å. The rod wall, two-atom thick, presents, in alternation with S atoms, Pb or (Pb,Sb) cations with prismatic coordination in the internal atom layer, while the external atom layer is constituted exclusively by Sb cations with dissymmetric square pyramidal coordination. A (Pb,Sb)2S2 fragment connects two successive rods along (2 0 1) to form a waffle-type palissadic layer. The unique O position, half filled, presents the same environment than the isolated O positions in the oxy-sulfide Pb14Sb30S54O5, or oxy-chloro-sulfides Pb18Sb20S46Cl2O and (Cu,Ag)2Pb21Sb23S55ClO. This compound belongs to a pseudo-homologous series of chalcogenides with waffle structure, ordered according to the size of their lozenge shape channel. Such a complex senary compound of the oxy-chloro-sulfide type illustrates the structural competition between three cations, on one hand, and, on the other hand, three anions. This compound is of special interest regarding the 1D distribution of magnetic Mn2+ atoms at the ∼2 nm scale. 相似文献
9.
Yuri L. Mikhlin Alexander S. Romanchenko Alexander A. Shagaev 《Applied Surface Science》2006,252(16):5645-5658
Natural n-type PbS single crystals have been studied using AFM, STM and STS after long-term oxidation in air at ambient temperatures and extensive etching in aqueous acid solutions, in contrast to previous work devoted to initial corrosion of fresh surfaces. The exposure of PbS to atmosphere at high relative humidity for several days yields widespread loose oxidation products; the process is much slower at low humidity. Surface morphologies diverge after the treatment in 1 M perchloric and hydrochloric acid solutions at room temperature and become widely different at elevated temperatures, displaying commonly etch pits up to several micrometers in size and depth along with rather uniformly distributed 20-100 nm protrusions of PbS phase. The changes both in topography and semiconducting properties of PbS found by tunneling spectroscopy have been explained in terms of the non-uniform distribution of donor- and acceptor-type defects D+/D− in the metal depleted surface layer, which are generated by chemical reactions and, in turn, determine the rates of the PbS corrosion. In particular, the D− centers exhibit a self-catalyzing effect on the non-oxidative local dissolution of PbS in HCl media, resulting in the deep etch pits. 相似文献
10.
H. Kuramochi J. Okabayashi F. Takano M. Mizuguchi T. Manago H. Akinaga 《Surface science》2004,550(1-3):192-198
Strong magnetic poles at characteristic rectangular defects have been observed using a magnetic force microscope on a MnAs(
1 0 0) thin film with the thickness of 30 nm. The MnAs thin film was epitaxially grown on a GaAs(0 0 1) substrate. The magnetic poles were in one-arranging direction, being independent of the magnetization direction of the film. The poles were pinned at the edges of the rectangular defects until just below the Curie temperature, and formed a stable magnetic-field loop on the MnAs surface. The stability of the magnetic pole pinning shows the distinctive feature of the magnetic domain structure on the surface with a strong anisotropy, which was built in the heterostructure of MnAs and GaAs. 相似文献