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111.
Semenov AN 《The European physical journal. E, Soft matter》2002,9(4):353-363
Adsorption of ideal polymers with stiff backbone onto a flat surface is considered theoretically. Both scaling approach and
quantitative theory are developed. We predict a self-similar monomer concentration profile c(x) ∼ x
-4/3 near the surface (when the distance to the surface x is much smaller than the chain persistence length l /2). The typical conformation of a weakly adsorbed chain can be viewed as a sequence of alternating flat (2-dimensional)
trains of wormlike short loops (flat blobs) and coil-like (3-dimensional) loops forming a triple-layer structure: contact
layer (x < Δ) of adsorbed fragments virtually laid on the surface, proximal layer (Δ < x < l) of flat blobs, and more dilute distal corona layer (x > l). Here Δ defines the range of monomer/surface attraction, Δ ≪ l. The adsorption transition is continuous. However, its relative width is small (T
* is the adsorption temperature, ΔT is the relevant temperature interval): ∼
, i.e. a discontinuous transition in the limit Δ/l↦ 0.
Received 10 October 2002 and Received in final form 22 November 2002
RID="a"
ID="a"Permanent address: Physics Department, Moscow State University, Moscow 119992, Russia. e-mail: semenov@polly.phys.msu.ru 相似文献
112.
取代基对双酞菁铥LB膜及光谱特性的影响 总被引:1,自引:0,他引:1
采用紫外-可见吸收光谱的方法研究了三种稀土夹心双酞菁铥化合物在溶液和LB膜中的聚集性和光谱特性。实验结果表明三种稀土双酞菁化合物在氯仿溶液中形成了H-聚集体,但当浓度比较低时,溶液中表现出单体的吸收。取代基OC8H17的加入使氯仿溶液中双酞菁铥化合物的聚集性减弱,而且使得吸收峰发生红移,对吸收峰的强度也有较大的影响,造成了Soret吸收带的分裂。另外,取代基OC8H17对LB膜中双酞菁分子的存在状态有较大的影响,在LB膜中,TmPc2和TmPcPc*分子以H-聚集体的形式存在,而TmPc*2分子以T-聚集体的形式存在。形成LB膜后,由于双酞菁分子之间排列紧密,相互作用加强,使得薄膜中分子聚集体的吸收峰相对于溶液中聚集体的吸收峰发生了一定的红移,薄膜中分子排列方向的不同对吸收光谱也有一定的影响。 相似文献
113.
金纳米空心半球壳膜的可调谐光学性质研究 总被引:1,自引:0,他引:1
以单层聚苯乙烯微球阵列为模板,通过控制其表面金膜蒸镀时间,制备了具有不同厚度的空心半球壳结构的金纳米膜.利用扫描电子显微镜和自制光谱仪分别测量了金膜表面形貌和其透射光谱,并分析了金膜形貌与其光学性质间的关系,同时以4-巯基苯胺为探针分子测定了金膜的表面增强喇曼散射效应.结果表明,该金纳米膜的表面等离子体共振波长随膜厚度增大而发生红移,在可见与近红外波段较宽范围内可调谐,并且,当金膜共振波长与入射激发光波长较近时,探针分子可产生出较强的表面增强喇曼信号.同时,对该现象的产生机制也进行了理论解释. 相似文献
114.
Monolayers of dioctadecyldimethylammonium bromide (DODA) at the air/water interface were used as model for charged surfaces
to study the adsorption of anionic polyelectrolytes. After spreading on a pure water surface the monolayers were compressed
and subsequently transferred onto a polyelectrolyte solution employing the Fromherz technique. The polyelectrolyte adsorption
was monitored by recording the changes in surface pressure at constant area. For poly(styrene sulfonate) and carboxymethylcellulose
the plot of the surface pressure as function of time gave curves which indicate a direct correlation between the adsorbed
amount and surface pressure as well as a solely diffusion controlled process. In the case of rigid rod-like poly(p-phenylene sulfonate)s the situation is more complicated. Plotting the surface pressure as function of time results in a curve
with sigmoidal shape, characterized by an induction period. The induction period can be explained by a domain formation, which
can be treated like a crystallization process. Employing the Avrami expression developed for polymer crystallization, the
change in the surface pressure upon adsorption of rigid rod-like poly(p-phenylene sulfonate)s can be described.
Received 1st July 2000 and Received in final form 7 December 2000 相似文献
115.
Ultrathin self-assembled polyelectrolyte multilayer membranes 总被引:3,自引:0,他引:3
B. Tieke F. van Ackern L. Krasemann A. Toutianoush 《The European physical journal. E, Soft matter》2001,5(1):29-39
The paper is concerned with ultrathin membranes prepared upon alternating layer-by-layer adsorption of cationic and anionic
polyelectrolytes on a porous substructure. The formation of the polyelectrolyte multilayer membranes is characterised and
the transport of gases, liquid mixtures and ions across the membranes is studied. In particular, the use of the membranes
for alcohol/water separation under pervaporation conditions, and for the separation of mono- and divalent ions is described.
It is demonstrated that upon a suitable choice of polyelectrolytes and substructures, and a careful optimisation of preparation
and operation conditions, membranes can be tailored exhibiting an excellent separation capability.
Received 4 September 2000 相似文献
116.
Several attempts have been already carried out in order to tether charged chains by an end at a free fluctuating surface.
We review here most of these attempts and focus on how close the physics of charged brushes can be investigated by such an
approach. We first describe results about films of charged-neutral diblock copolymers spread at the surface of water. Results
can be mostly rationalized in terms of charged brushes although additional structurations and fluctuations of the interface
can be observed. The latter deformations are also observed when adsorbed layers of charged-neutral diblock copolymers are
considered. At last, we examine how free suspended films of charged-neutral diblock copolymers can be viewed as two opposing
charged brushes, both in terms of thickness and pressure.
Received 9 May 2000 相似文献
117.
由有机LB膜技术发展了一种制备组分、厚度可控的无机超薄陶瓷膜的方法.以Zr、 Y的β-二酮络合物的作为"表面离子"代替传统的亚相离子,沉积它们与花生酸的混合LB膜.并将它作为前驱物,经臭氧处理和热处理,成功制得了Y2O3稳定的立方相ZrO2超薄膜(YSZ).用X射线衍射(XRD)、 X射线光电子能谱(XPS)等手段研究了YSZ薄膜的相结构和其组成.结果表明,超薄陶瓷膜中Zr与Y的含量比率控制得很好,且形成Y2O3稳定的立方相ZrO2.说明这种方法可以成功地用来制备组分和膜厚均可控的纳米陶瓷膜. 相似文献
118.
以含有共轭大π键的2,5-双(乙炔基二茂铁)噻吩(BFET)和二甲基双十八烷基铵(DMDOA)与Keggin结构和Dawson结构钨磷杂多酸做成膜材料, 用LB技术组装了两种新型无机-有机杂化LB膜. 用π-A曲线、UV-vis吸收光谱、原子力显微镜(AFM)、扫描隧道显微镜(STM)、荧光光谱和表面光电压谱(SPS)对标题LB膜的成膜性能、结构及光电性质进行了研究, 发现标题杂化LB膜的粒子具有纳米尺寸, 在可见光区有较强的光电压响应, 在电压为±2.0 V时, 隧道电流值达到±100 nA. 相似文献
119.
采用LB技术组装了一种三维有序的由十八胺修饰的纳米金颗粒多层结构.这是一种新的组装纳米颗粒三维有序聚集体的方法.为了扩大这种方法的适用范围,在组装过程中,将有机小分子1-苯基-5-巯基四氮唑引进结构,形成了新的纳米金颗粒多层聚集体.这两种多层膜经透射电子显微镜和小角X射线衍射测量证明构成多层膜的单层膜上的纳米金颗粒是有序的,并且颗粒在层与层之间的排列也是有序的. 相似文献
120.
Fiona Regan Fiona Walsh James Walsh 《International journal of environmental analytical chemistry》2013,93(7-8):621-631
A novel plasticised PVC polymer membrane as a sensing film for the determination of BTEX compounds using ATR-FTIR spectroscopy is demonstrated. A range of 10 plasticised PVC phases have been investigated using toluene and tetrachloroethylene as test analytes. Both analyte enrichment rates and infrared absorbance values were considered when choosing a suitable polymer for sensing. An enhancement in analyte absorbance at the characteristic IR absorption bands was noted as the plasticiser concentration in the film was increased. 2% PVC with 75% diisooctyl azelate was found to show promising results for simultaneous determination of the BTEX compounds. All BTEX analytes can be measured in less than 8 min. A study of a multicomponent sample demonstrated that analyte enrichment times were influenced by the presence of even one additional analyte component in the sample. 相似文献