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991.
992.
In this work, we designed and studied a feasible dual-layer binary metagrating, which can realize controllable asymmetric transmission and beam splitting with nearly perfect performance. Owing to ingenious geometry configuration, only one meta-atom is required to design for the metagrating system. By simply controlling air gap between dual-layer metagratings, high-efficiency beam splitting can be well switched from asymmetric transmission to symmetric transmission. The working principle lies on gap-induced diffraction channel transition for incident waves from opposite directions. The asymmetric/symmetric transmission can work in a certain frequency band and a wide incident range. Compared with previous methods using acoustic metasurfaces, our approach has the advantages of simple design and tunable property and shows promise for applications in wavefront manipulation, noise control and one-way propagation. 相似文献
993.
994.
Haitao Han Liang Kan Ping Li Guoshuai Zhang Kaiyue Li Wuping Liao Yunling Liu Wei Chen Chunhua T.Hu 《中国科学:化学(英文版)》2021,(3):426-431
Three 4.8 nm isostructural{M72}(M=CoⅡ for CIAC-128,NiⅡ for CIAC-129,FeⅡ for CIAC-130) metal-organic polyhedra(MOPs) are constructed by eighteen M4-p-tert-butylthiacalix[4]arene (M4-TC4A) units bridged via sixteen four-connected 5,5′-(1H-1,2,4-triazole-3,5-diyl) diisophthalic acid (H4TADIPA) linkers.These MOPs are featured with a rarely reported concave coordination cage,which can be simplified as a squeezed double-decker hexagonal prism pressed from the top and bottom hexagonal faces.Furthermore,CIAC-128,CIAC-129 and CIAC-130 are the highest nuclearity discrete clusters of Co,Ni and Fe reported so far.CIAC-128 has higher separation selectivity of C3H8 than CH4 under ambient conditions,and also exhibits separation selectivity for C2H6/CH4,C2H2/CH4,and C2H4/CH4.In addition,CIAC-128 can provide the cavity for the confined synthesis of noble metal nanoclusters such as Pd nanoclusters and the resulting Pd@CIAC-128 hybrids show higher electrocatalytic activity than commercial Pt/C towards hydrogen evolution reaction (HER). 相似文献
995.
996.
997.
AbstractIn this study, as a continuous effort for searching efficient blue-emitting materials, we designed and synthesized materials based on indeno[1,2-a]arene. OLED devices using these materials were fabricated in the following sequence; ITO (180?nm)/N,N'-diphenyl-N,N'-(2-napthyl)-(1,1'-phenyl)-4,4'-diamine (NPB) (50?nm)/emitting materials (30?nm)/4,7-diphenyl-1,10-phenanthroline (Bphen) (30?nm)/Liq/Al (2/100?nm). Particularly, a device using 7,7-dimethyl-7H-indeno[1,2-a]pyrene as emitter showed maximum values of luminous efficiency, power efficiency, and external quantum efficiency of 1.10?cd/A, 0.49?lm/W, 1.47% at 20?mA/cm2, respectively with CIE (x,y) coordinates of (0.15, 0.08) at 6.0V. 相似文献
998.
为研究泄压膜约束条件对甲烷/空气预混气体爆炸压力特性的影响,在方形火焰燃烧传播测试管道中布置压力传感器,开展不同泄压膜材料、泄压膜层数及泄压口位置实验。结果表明:牛皮纸和聚丙烯薄膜约束泄爆过程中,每增加一层泄压膜,管道内最大泄爆压力平均上升11.2%和12.3%。各强度泄压膜约束条件下,管道内最大泄爆压力随着泄压口位置接近点火端,均呈现Z形规律,当泄压口设置在距尾部端面0.25 m时,各曲线达到最小值,当泄压口设置在距尾部端面0.50 m时,各曲线出现最大值。 相似文献
999.
Shoichi Maeda Shunta Chikami Glenn Villena Latag Subin Song Norio Iwakiri Tomohiro Hayashi 《Molecules (Basel, Switzerland)》2022,27(7)
In this paper, we propose a new spectroscopic method to explore the behavior of molecules near polymeric molecular networks of water-containing soft materials such as hydrogels. We demonstrate the analysis of hydrogen bonding states of water in the vicinity of hydrogels (soft contact lenses). In this method, we apply force to hydrated contact lenses to deform them and to modulate the ratio between the signals from bulk and vicinal regions. We then collect spectra at different forces. Finally, we extracted the spectra of the vicinal region using the multivariate curve resolution-alternating least square (MCR-ALS) method. We report the hydration states depending on the chemical structures of hydrogels constituting the contact lenses. 相似文献
1000.
Rate Coefficients and Kinetic Isotope Effects of Cl+XCl→XCl+Cl (X=H,D, Mu) Reactions from Ring Polymer Molecular Dynamics 下载免费PDF全文
The ring-polymer molecular dynamics (RPMD) was used to calculate the thermal rate coefficients and kinetic isotope effects of the heavy-light-heavy abstract reaction Cl+XCl\begin{document}$ \rightarrow $\end{document} XCl+Cl (X = H, D, Mu). For the Cl+HCl reaction, the excellent agreement between the RPMD and experimental values provides a strong proof for the accuracy of the RPMD theory. And the RPMD results are also consistent with results from other theoretical methods including improved-canonical-variational-theory and quantum dynamics. The most novel finding is that there is a double peak in Cl+MuCl reaction near the transition state, leaving a free energy well. It comes from the mode softening of the reaction system at the peak of the potential energy surface. Such an explicit free energy well suggests strongly there is an observable resonance. And for the Cl+DCl reaction, the RPMD rate coefficient again gives very accurate results compared with experimental values. The only exception is at the temperature of 312.5 K, results from RPMD and all other theoretical methods are close to each other but slightly lower than the experimental value, which indicates experimental or potential energy surface deficiency. 相似文献