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151.
Mechanical Characterization Measurement of Polymer Material under Stress by Birefringence Microscope
Some polymer materials under tensile stress provide us interesting information. Internal structure changes of polymer materials
must be observed by external stress. Birefringence shows the orientation characteristic in molecular orientation. A microscopic
measurement system for birefringence distribution is proposed to analyze the relation between applied stress and birefringence
distribution of an internal structure. Birefringence distributions of gelatin such as phase difference and azimuthal angle
are shown in cases of loading and unloading stress as a demonstration. The phase difference increased nonlinearly with each
process, and change of birefringence in the elastic domain was different from that in the plastic domain. 相似文献
152.
Norihiro Fukuchi Ye Biqing Yasunori Igasaki Narihiro Yoshida Yuji Kobayashi Tsutomu Hara 《Optical Review》2005,12(5):372-377
We have developed optically-addressed and electrically-addressed liquid crystal spatial phase-only light modulators having
no pixelized structures. We obtained a large depth of phase-only modulation and high diffraction efficiency based on the electro-optical
characteristics of a parallel-aligned nematic liquid crystal. These spatial light modulators (SLM) are of the reflection type,
so there would be a loss of power in the readout light from the half mirror, which was set up so as to separate the incident
and reflected lights. To optimize the characteristics of a reflection type spatial phase-only light modulator, we have proposed
an oblique incident optical readout setup. We have examined the effect of conditions such as the polarization direction and
the incidence angle of the readout light, and the orientation of liquid crystal molecules in the SLM. High diffraction efficiency
close to the theoretical maximum value was obtained by adjusting the above conditions. The simulation analysis can well explain
the experimental results of phase modulation. 相似文献
153.
This paper describes the three-dimensional flow structure in grooved channels with different cavity lengths at intermediate
Reynolds numbers. For steady flow, the three-dimensional effects are dominant near the side walls of the channel. However,
after the onset of self-sustained oscillatory flow due to Tollmien–Schlichting waves as the primary instability, a secondary
instability produces a three-dimensional flow with Taylor–Geortler-like vortical structure, at the bottom of the groove. This
trend becomes more significant as the cavity length increases. Furthermore, the reason for three-dimensional flow is discussed
using additional numerical analysis, and it is confirmed that the source of three-dimensional instability is the groove vortices
due to the presence of side walls, rather than the channel traveling wave.
Received: 7 September 1999/Accepted: 11 November 2000 相似文献
154.
Laguerre-Gaussian (LG) beams of various higher-order radial modes are generated by using a reflective phase-only liquid crystal on silicon (LCOS) spatial light modulator (SLM). Because of the LCOS SLM's phase-modulation characteristic of a wide spatial bandwidth, a phase modulation scheme effectively generates higher-order LG beams of up to the fifth-order radial mode. We also perform correlation analyses between the observed and the theoretical two-dimensional mode profiles to universally obtain correlation coefficients of more than 0.946, which suggest mode generations of high quality. 相似文献
155.
Yasuhiro Shiraishi Yugo Furubayashi Go Nishimura Takayuki Hirai 《Journal of luminescence》2007,127(2):623-632
Dinuclear lanthanide (Ln=Tb3+ or Eu3+) complexes (Ln2L2) of two octadentate macrocyclic polyaminopolycarboxylic ligands connected through a benzophenone (BP) moiety (L2) have been synthesized. Sensitized luminescence properties of Ln2L2 in water have been studied in comparison to those of BP-conjugated mononuclear Ln complexes (LnL1). The luminescence intensity of Tb2L2 is lower than that of TbL1 because of lower triplet quantum yield of the BP moiety. In contrast, Eu2L2 shows higher intensity than EuL1. For both Eu complexes, energy level of triplet excited-state BP (3BP*) is only 3 kJ mol−1 higher than that of 5D2 excited-state of Eu3+. The 5D2 state formed by a triplet-energy transfer (TET) from 3BP* is therefore deactivated by a back energy transfer (BET) to the ground-state BP, resulting in low luminescence intensity of EuL1. In contrast, within Eu2L2, TET from 3BP* to 5D0 state of two Eu3+ ions is accelerated, thus leading to higher luminescence intensity. Another notable feature of Eu2L2 is the luminescence quantum yield independent of its concentration. In contrast, for EuL1 system, an intermolecular BET occurs from 5D2 state of Eu3+ to the ground-state BP conjugated to another EuL1 complex, resulting in a yield decrease with the concentration increase. 相似文献
156.
Superstructure in the Metastable Intermediate‐Phase Li2/3FePO4 Accelerating the Lithium Battery Cathode Reaction 下载免费PDF全文
Dr. Shin‐ichi Nishimura Ryuichi Natsui Prof. Atsuo Yamada 《Angewandte Chemie (International ed. in English)》2015,54(31):8939-8942
LiFePO4 is an important cathode material for lithium‐ion batteries. Regardless of the biphasic reaction between the insulating end members, LixFePO4, x≈0 and x≈1, optimization of the nanostructured architecture has substantially improved the power density of positive LiFePO4 electrode. The charge transport that occurs in the interphase region across the biphasic boundary is the primary stage of solid‐state electrochemical reactions in which the Li concentrations and the valence state of Fe deviate significantly from the equilibrium end members. Complex interactions among Li ions and charges at the Fe sites have made understanding stability and transport properties of the intermediate domains difficult. Long‐range ordering at metastable intermediate eutectic composition of Li2/3FePO4 has now been discovered and its superstructure determined, which reflected predominant polaron crystallization at the Fe sites followed by Li+ redistribution to optimize the Li? Fe interactions. 相似文献
157.
Hydroxoiridium/Chiral Diene Complexes as Effective Catalysts for Asymmetric Annulation of α‐Oxo‐ and Iminocarboxamides with 1,3‐Dienes 下载免费PDF全文
Miyuki Hatano Dr. Takahiro Nishimura 《Angewandte Chemie (International ed. in English)》2015,54(37):10949-10952
The asymmetric [3+2] annulation of α‐oxo‐ and α‐iminocarboxamides with 1,3‐dienes catalyzed by hydroxoiridium/chiral diene complexes was realized, giving high yields of the corresponding γ‐lactams with high enantioselectivity. 相似文献
158.
Iron–Oxalato Framework with One‐Dimensional Open Channels for Electrochemical Sodium‐Ion Intercalation 下载免费PDF全文
Dr. Xianfen Wang Ryosuke Kurono Dr. Shin‐ichi Nishimura Dr. Masashi Okubo Prof. Atsuo Yamada 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(3):1096-1101
Discovery of a new class of ion intercalation compounds is highly desirable due to its relevance to various electrochemical devices, such as batteries. Herein, we present a new iron–oxalato open framework, which showed reversible Na+ intercalation/extraction. The hydrothermally synthesized K4Na2[Fe(C2O4)2]3 ? 2 H2O possesses one‐dimensional open channels in the oxalato‐bridged network, providing ion accessibility up to two Na+ per the formula unit. The detailed studies on the structural and electronic states revealed that the framework exhibited a solid solution state almost entirely during Na+ intercalation/extraction associated with the reversible redox of Fe. The present work demonstrates possibilities of the oxalato frameworks as tunable and robust ion intercalation electrode materials for various device applications. 相似文献
159.
Nakayama Masanobu Nishimura Norimitsu Kondo Yuki Takeda Hayami Kasuga Toshihiro 《Journal of Solid State Electrochemistry》2017,21(4):1137-1143
Journal of Solid State Electrochemistry - We demonstrate the Laplace transform (LT) impedance technique for measuring electrochemical lithiation and delithiation in the two-phase system of spinel... 相似文献
160.
Rui UmedaTakashi Nishimura Kenta KaibaToshimasa Tanaka Yuuki TakahashiYutaka Nishiyama 《Tetrahedron》2011,67(38):7217-7221
It was found that rhenium complex was an efficient catalyst for the acylative cleavage of C-O bond of ethers with acyl chlorides. When acyclic ethers were allowed to react with acyl chlorides in the presence of a catalytic amount of ReBr(CO)5, acylative cleavage of C-O bond of acyclic ethers smoothly proceeded to give the corresponding esters in moderate to good yields. Similarly, cyclic ethers were acylative cleaved by acyl chlorides to give the corresponding chloro substituted esters in good yields by the use of Re2O7 catalyst. 相似文献