全文获取类型
收费全文 | 42501篇 |
免费 | 12074篇 |
国内免费 | 1663篇 |
专业分类
化学 | 41963篇 |
晶体学 | 343篇 |
力学 | 523篇 |
综合类 | 20篇 |
数学 | 2116篇 |
物理学 | 3036篇 |
无线电 | 8237篇 |
出版年
2024年 | 16篇 |
2023年 | 95篇 |
2022年 | 96篇 |
2021年 | 262篇 |
2020年 | 1860篇 |
2019年 | 3271篇 |
2018年 | 1511篇 |
2017年 | 1095篇 |
2016年 | 4025篇 |
2015年 | 4167篇 |
2014年 | 4146篇 |
2013年 | 4702篇 |
2012年 | 3513篇 |
2011年 | 2722篇 |
2010年 | 3281篇 |
2009年 | 3290篇 |
2008年 | 2750篇 |
2007年 | 2119篇 |
2006年 | 1771篇 |
2005年 | 1912篇 |
2004年 | 1649篇 |
2003年 | 1541篇 |
2002年 | 2185篇 |
2001年 | 1504篇 |
2000年 | 1428篇 |
1999年 | 461篇 |
1998年 | 113篇 |
1997年 | 111篇 |
1996年 | 86篇 |
1995年 | 61篇 |
1994年 | 60篇 |
1993年 | 47篇 |
1992年 | 37篇 |
1991年 | 39篇 |
1990年 | 29篇 |
1989年 | 24篇 |
1988年 | 25篇 |
1987年 | 18篇 |
1986年 | 20篇 |
1985年 | 22篇 |
1984年 | 19篇 |
1983年 | 13篇 |
1982年 | 17篇 |
1981年 | 23篇 |
1980年 | 12篇 |
1979年 | 14篇 |
1977年 | 14篇 |
1976年 | 7篇 |
1974年 | 11篇 |
1972年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 450 毫秒
81.
The development of the poly(3‐hydroxybutyrate) (PHB) morphology in the presence of already existent poly(vinylidene fluoride) (PVDF) spherulites was studied by two‐stage solidification with two separate crystallization temperatures. PVDF formed irregular dendrites at lower temperatures and regular, banded spherulites at elevated temperatures. The transition temperature of the spherulitic morphology from dendrites to regular, banded spherulites increased with increasing PVDF content. A remarkable amount of PHB was included in the PVDF dendrites, whereas PHB was rejected into the remaining melt from the banded spherulites. When PVDF crystallized as banded spherulites, PHB could consequently crystallize only around them, if at all. In contrast, PHB crystallized with a common growth front, starting from a defined site in the interfibrillar regions of volume‐filling PVDF dendrites. It formed by itself dendritic spherulites that included a large number of PVDF spherulites. For blends with a PHB content of more than 80 wt %, for which the PVDF dendrites were not volume‐filling, PHB first formed regular spherulites. Their growth started from outside the PVDF dendrites but could later interpenetrate them, and this made their own morphology dendritic. These PHB spherulites melted stepwise because the lamellae inside the PVDF dendrites melted at a lower temperature than those from outside. This reflected the regularity of the two fractions of the lamellae because that of those inside the dendrites of PVDF was controlled by the intraspherulitic order of PVDF, whereas that from outside was only controlled by the temperature and the melt composition. The described morphologies developed without mutual nucleating efficiency of the components. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 873–882, 2003 相似文献
82.
A lithium(I) coordination polymer has been formed from LiClO4 and the 2,2′‐bipyrimidine (bpym) ligand in which each square pyramidal lithium(I) atom is coordinated in the basal plane by four nitrogen donor atoms derived from two bpym ligands and one water molecule at the apical position. These are connected into a layer structure via hydrogen‐bonding interactions involving the perchlorate anions. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
83.
84.
A 2D HgII coordination polymer containing ligands 1,2,4‐triazole (Htrz) and thiocyanate, [Hg(μ3‐trz)(SCN)]n ( 1 ) has been synthesized and characterized by elemental analysis and IR spectroscopy. The single‐crystal X‐ray data show the coordination number of Hg atoms is four and the ligand trz? acts as a three‐fold donor. The thermal stability of compound 1 was studied by thermal gravimetric and differential thermal analyses. The composition and formation of the complex in methanol solution were found to be in support of its solid state structure. 相似文献
85.
Zi‐Niu Wu 《国际流体数值方法杂志》2005,48(5):541-564
The widely used locally adaptive Cartesian grid methods involve a series of abruptly refined interfaces. In this paper we consider the influence of the refined interfaces on the steady state errors for second‐order three‐point difference approximations of flow equations. Since the various characteristic components of the Euler equations should behave similarly on such grids with regard to refinement‐induced errors, it is sufficient enough to conduct the analysis on a scalar model problem. The error we consider is a global error, different to local truncation error, and reflects the interaction between multiple interfaces. The steady state error will be compared to the errors on smooth refinement grids and on uniform grids. The conclusion seems to support the numerical findings of Yamaleev and Carpenter (J. Comput. Phys. 2002; 181: 280–316) that refinement does not necessarily reduce the numerical error. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
86.
Mao‐Chuan Yuan Ping‐I Shih Chen‐Han Chien Ching‐Fong Shu 《Journal of polymer science. Part A, Polymer chemistry》2007,45(14):2925-2937
We have synthesized a blue‐light‐emitting polyfluorene (PF) derivative ( PF‐CBZ‐OXD ) that presents bulky hole‐transporting carbazole and electron‐transporting oxadiazole pendent groups functionalized at the C‐9 positions of alternating fluorene units. The results from photoluminescence and electrochemical measurements indicate that both the side chains and the PF main chain retain their own electronic characteristics in the copolymer. An electroluminescent device incorporating this polymer as the emitting layer was turned on at 4.5 V; it exhibited a stable blue emission with a maximum external quantum efficiency of 1.1%. Moreover, we doped PF‐CBZ‐OXD and its analogue PF‐TPA‐OXD with a red‐light‐emitting iridium phosphor for use as components of phosphorescent red‐light emitters to investigate the effect of the host's HOMO energy level on the degree of charge trapping and on the electrophosphorescent efficiency. We found that spectral overlap and individual energy level matching between the host and guest were both crucial features affecting the performance of the electroluminescence devices. Atomic force microscopy measurements indicated that the dipolar nature of PF‐CBZ‐OXD , in contrast to the general nonpolarity of polydialkylfluorenes, provided a stabilizing environment that allowed homogeneous dispersion of the polar iridium triplet dopant. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 2925–2937, 2007 相似文献
87.
Recent technological advances have made it possible to support long lifetime and large volume streaming data transmissions
in sensor networks. A major challenge is to maximize the lifetime of battery-powered sensors to support such transmissions.
Battery, as the power provider of the sensors, therefore emerges as the key factor for achieving high performance in such
applications. Recent study in battery technology reveals that the behavior of battery discharging is more complex than we
used to think. Battery powered sensors might waste a huge amount of energy if we do not carefully schedule and budget their
discharging. In this paper we study the effect of battery behavior on routing for streaming data transmissions in wireless
sensor networks. We first give an on-line computable energy model to mathematically model battery discharge behavior. We show
that the model can capture and describe battery behavior accurately at low computational complexity and thus is suitable for
on-line battery capacity computation. Based on this battery model we then present a battery-aware routing (BAR) protocol to
schedule the routing in wireless sensor networks. The routing protocol is sensitive to the battery status of routing nodes
and avoids energy loss. We use the battery data from actual sensors to evaluate the performance of our protocol. The results
show that the battery-aware protocol proposed in this paper performs well and can save a significant amount of energy compared
to existing routing protocols for streaming data transmissions. Network lifetime is also prolonged with maximum data throughput.
As far as we know, this is the first work considering battery-awareness with an accurate analytical on-line computable battery
model in sensor network routing. We believe the battery model can be used to explore other energy efficient schemes for wireless
networks as well. 相似文献
88.
Calculations and detailed first principle and thermodynamic analyses have been performed to understand the formation mechanism of K2Ti6O13 nanowires (NWs) by a hydrothermal reaction between bulk Na2Ti3O7 crystals and a KOH solution. It is found that direct ion exchange between K+ and Na+ plus H+ interactions with [TiO6] octahedra in Na2Ti3O7 promote the formation of an intermediate H2K2Ti6O14 phase. The large lattice mismatch between this intermediate phase and the bulk Na2Ti3O7 structure, and the large energy reduction associated with the formation of this intermediate phase, drive the splitting of the bulk crystal into H2K2Ti6O14 NWs. However, these NWs are not stable because of large [TiO6] octahedra distortion and are subject to a dehydration process, which results in uniform K2Ti6O13 NWs with narrowly distributed diameters of around 10 nm. 相似文献
89.
S. K. Chen A. Serquis G. Serrano K. A. Yates M. G. Blamire D. Guthrie J. Cooper H. Wang S. Margadonna J. L. MacManus‐Driscoll 《Advanced functional materials》2008,18(1):113-120
By applying a combination of characterisation tools, changes in structural and superconducting properties with nominal Mg non‐stoichiometry in MgxB2 are found. The non‐stoichiometry produces enhanced in‐field critical current densities (Jc's) and upper critical field / irreversibility field (Hc2/Hirr(T)) values. Upper critical fields of ~ 21 T (4.2 K) were obtained in nominal Mg‐deficient samples compared to ~ 17 T (4.2 K) for near‐stoichiometric samples. 相似文献
90.
In this paper we consider the numerical approximation of steady and unsteady generalized Newtonian fluid flows using divergence free finite elements generated by the Powell–Sabin–Heindl elements. We derive a priori and a posteriori finite element error estimates and prove convergence of the method of successive approximations for the steady flow case. A priori error estimates of unsteady flows are also considered. These results provide a theoretical foundation and supporting numerical studies are to be provided in Part II. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献