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Light Irradiation through Small Particles and Its Applications for Surface Nanostructuring in Near Field 下载免费PDF全文
We investigate the light scattering through small particles and its applications in nanostructuring, such as nanobumping, nanopatterning and dry laser cleaning. The theoretical calculation based on Mie theory provides an exact solution for sphere cavity resonance and plasmon resonance, which are two mechanisms for dielectric and metallic particles assisted surface nanostructuring in near field. The experimental results indicate that nanobumps on glass surface and subwavelength holes array on silicon surface can be formed without cracks with the self-assembly of 1 μm silica particle mask under laser irradiation. It is also found that the scattering wave by 40 nm gold particles can propagate 200 times away in terms of particle radius as recorded by photoresist under the UV light irradiation. Meanwhile, dry laser cleaning of 40nm gold particle on silicon wafer is demonstrated at plasmonic resonance frequency. The total cleaning efficiency is estimated to be 80%. 相似文献
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采用标准回流法和仪器法(用COD速测仪)对工业废水化学需氧量进行对照测定,结果发现,用COD速测仪测定工业废水,简便、快速、精密度好、准确度高。 相似文献
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Pseudo‐first‐order rate constants (kobs) for tertiary amine (DABCO and Me3N) buffer‐catalyzed cyclization of N′‐morpholino‐N‐(2′‐methoxyphenyl)phthalamide ( 1 ) to N‐(2′‐methoxyphenyl)phthalimide ( 2 ) reveal saturation (nonlinear) plots of kobs versus [Buf]T (total tertiary amine buffer concentration) at a constant pH. Such plots at different pH have been attributed to the presence of a reactive intermediate (T?) formed by tertiary amine buffer‐catalyzed intramolecular nucleophilic addition of the secondary amide nitrogen to the carbonyl carbon of the tertiary amide group of 1 . © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 263–272, 2010 相似文献
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Hong‐Cheu Lin Meng‐Dan Jiang Shen‐Chang Wu Leng‐Long Jou Kai‐Pin Chou Ching‐Mao Huang Kung‐Hwa Wei 《Journal of polymer science. Part A, Polymer chemistry》2009,47(18):4685-4702
A series of diblock‐copolymers were synthesized through anionic polymerization of styrene and tert‐butyl methacrylate (tBuA) with different monomer ratios, and analogous block‐copolymeric derivatives (PS‐b‐PAA)s with monofunctional carboxylic acid groups were obtained by further hydrolyzation as hydrogen‐bonded (H‐bonded) proton donors. Via H‐bonded interaction, these diblock‐coplymeric donors (PS‐b‐PAA)s were incorporated with luminescent mono‐pyridyl/bis‐pyridyl acceptors to form single/double H‐bonded supramolecules, that is, H‐bonded side‐chain/cross‐linking copolymers, respectively. The supramolecular architectures formed by donor polymers and light‐emitting acceptors were influenced by the ratio of acid blocks in the diblock copolymeric donors and the type of single/double H‐bonded light‐emitting acceptors. Their thermal and luminescent properties can be adjusted by H‐bonds, and more than 100 nm of red‐shifted photoluminescence (PL) emissions were observed, which depend on the degrees of the H‐bonding interactions. Self‐assembled phenomena of amphiphilic dibolck copolymers and their H‐bonded complexes were confirmed by TEM micrographs, and supramolecular microphase separation of spherical micelle‐like morphology was demonstrated to affect the photophysical properties. Polymer light‐emitting diode (PLED) devices containing H‐bonded complexes showed electroluminescence (EL) emissions of 503–560 nm under turn‐on voltages of 7.5–9.0 V, maximum power efficiencies of 0.23–0.37 cd/A (at 100 mA/cm2), and maximum luminances of 318–519 cd/m2 (around 25 V). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4685–4702, 2009 相似文献
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实验研究了正色散固体介质中的激光脉冲自压缩现象,证明了无需任何外加色散补偿情况下,固体透明介质中的自聚焦传输过程可使高功率飞秒激光脉冲实现时域脉冲压缩,并详细研究了输出脉冲的时域和频域特性随入射脉冲强度的演化规律.实验结果表明脉冲自压缩量随入射脉冲强度的增加呈递增趋势,然而当入射光强增大到足以引起超连续谱及锥形辐射产生时,脉冲时域形状会发生分裂.此外还发现发散光束入射情况下同样可以观察到脉冲自压缩现象.
关键词:
超短激光脉冲
脉冲压缩
非线性传输 相似文献
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Su?Liu Xueqi?Leng Xu?Wang Qianqian?Pei Xuejun?Cui Yu?WangEmail author Jiadong?Huang 《Mikrochimica acta》2017,184(7):1969-1976
The authors describe a colorimetric method for the determination of Hg(II) ion. It is based on the color change from red to colorless as displayed by gold nanoparticle (AuNP) modified with thymine - rich DNA. Signal amplification is accomplished by free strand displacement recycling. In this strategy, Hg(II) unfolds the arch-trigger duplex due to the high affinity between Hg(II) and the thymines to form T-Hg(II)-T structures, thereby causing the release of trigger. The liberated trigger unfolds the hairpin structure of H1, and unfolded H1 further unfolds with H2. As a result, the H2 hairpin displaces trigger, and the released trigger unfolds another H1. This results in strong and enzyme-free strand displacement recycling amplification. The aggregation of DNA-AuNPs occurs in the presence of the duplex formed by hairpins H2 and H1. This results in a color change from red to colorless that can be visually observed. Under optimal conditions, the assay has a detection range over 4 orders of magnitude and a 3.4 nM detection limit. The assay is selective, sensitive, rapid and cost-effective. In our perception, it represents a useful platform for determination of Hg(II). 相似文献
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A new dual chemosensor (TTF-PBA) for Fe3+ and Cu2+ in different signal pathways was designed and synthesized. The absorption spectrum, fluorescence spectrum and cyclic voltammograms changed in the presence of Cu2+ and Fe3+. The optical color changed within 5 s from yellow to orange upon the addition of Cu2+, and it changed to dark yellow when Fe3+ existed. The cyclic voltammogram of Cu2+/TTF-PBA changed from Eox = 0.50 V, Ered = 0.32 V to Eox = 0.64 V, Ered = 0.80 V (vs Ag/AgCl) upon the addition of 2.0 equiv. Cu2+. As for Fe3+/TTF-PBA, its oxidation wave disappeared, and its reduction wave appeared at Ered = ?0.59 V (vs Ag/AgCl) upon the addition of 4.0 equv. Fe3+. The sensor displayed high selectivity for Cu2+ and Fe3+ over other ions including Pb2+, Zn2+, Ni2+, Ag+, Cr3+, Mn2+, Al3+, Co2+, Pd2+, Hg2+, Fe2+, Cd2+, Ce3+, Bi3+ and Au3+, the detection limits for Cu2+ and Fe3+ ion reached as low as 5.33 × 10?7 mol/L and 5.34 × 10?7 mol/L, respectively. Furthermore, when Fe3+ existed, Cu2+ can be detected sequentially by the sensor through the absorption spectrum and the color change observed by naked-eyes. 相似文献