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861.
Chun-Gil Park 《数学物理学报(B辑英文版)》2003,23(1)
All C*-algebras of sections of locally trivial C* -algebra bundles over ∏i=1sLki(ni) with fibres Aw Mc(C) are constructed, under the assumption that every completely irrational noncommutative torus Aw is realized as an inductive limit of circle algebras, where Lki (ni) are lens spaces. Let Lcd be a cd-homogeneous C*-algebra over whose cd-homogeneous C*-subalgebra restricted to the subspace Tr × T2 is realized as C(Tr) A1/d Mc(C), and of which no non-trivial matrix algebra can be factored out.The lenticular noncommutative torus Lpcd is defined by twisting in by a totally skew multiplier p on Tr+2 × Zm-2. It is shown that is isomorphic to if and only if the set of prime factors of cd is a subset of the set of prime factors of p, and that Lpcd is not stablyisomorphic to if the cd-homogeneous C*-subalgebra of Lpcd restricted to some subspace LkiLki (ni) is realized as the crossed product by the obvious non-trivial action of Zki on a cd/ki-homogeneous C*-algebra over S2ni+1 for ki an integer greater than 相似文献
862.
J.H. Yu J.H. Kim D.S. Park T.S. Kim T.S. Jeong C.J. Youn K.J. Hong 《Journal of Crystal Growth》2010,312(10):1683-1686
Wide band-gap BeZnO layers were grown on Al2O3 (0 0 0 1) substrate using radio-frequency magnetron co-sputtering. The rate of BexZn1−xO crystallized as a hexagonal structure was x=0.2. From the X-ray photoelectron spectroscopy measurement, the O–Zn bonds relating the crystal structure and the Be–O bonds related to the deviation of the stoichiometry in the BeZnO layer were caught at 530.4 and 531.7 eV in the O 1s spectrum, respectively. Thus, the observance on the Be 1s peak of 113.2 eV associated with the bonding Be–O indicates that the sputtered Be atoms are substituted for the host-lattice site in ZnO. This Be–O bonding shows a relatively low intense and broadening spectrum caused by large fluctuation of Be content in the BeZnO layer. From the photoluminescence and transmittance measurement, the free exciton and the neutral donor-bound exciton (D0, X) emissions were observed at 3.7692 and 3.7313 eV, respectively, and an average transmittance rate over 95% was achieved in a wide ultraviolet (UV)–visible region. Also, the binding energy for the (D0, X) emission was extracted to be 37.9 meV. Through the wide band-gap material BeZnO, we may open some possibilities for fabricating a ZnO-based UV light-emitting diode to be utilized as a barrier layer comprised of the ZnO/BeZnO quantum well structure and/or an UV light emitting material itself. 相似文献
863.
Si-Young Kim Hyun-Jae Lee Seung-Hwan Park Woong Lee Mi-Na Jung Katsushi Fujii Takenari Goto Takashi Sekiguchi Jiho Chang Gyungsuk Kil Takafumi Yao 《Journal of Crystal Growth》2010,312(14):2150-2153
A new hydride vapor phase epitaxy (HVPE)-based approach for the fabrication of freestanding GaN (FS-GaN) substrates was investigated. For the direct formation of low-temperature GaN (LT-GaN) layers, the growth parameters were optimized: the polarity of ZnO, the growth temperature, and the V/III ratio. The FS-GaN layer was achieved by gas etching in an HVPE reactor. A fingerprint of Zn out-diffusion was detected in the photoluminescence measurements, especially for the thin (80 μm) FS-GaN film; however, a thicker film (400 μm) was effectively reduced by optimization of GaN growth. 相似文献
864.
Jang-Jung Kim Sook-Hyun Kim Seung-Wook Suh Dong-Uk Choe Byung-Ki Park Jae-Rock Lee Young-Seak Lee 《Journal of Crystal Growth》2010,312(22):3410-3415
Polycrystalline Bi2Te3 nanowires were prepared by a hydrothermal method that involved inducing the nucleation of Bi atoms reduced from BiCl3 on the surface of Te nanowires, which served as sacrificial templates. A Bi–Te alloy is formed by the interdiffusion of Bi and Te atoms at the boundary between the two metals. The Bi2Te3 nanowires synthesized in this study had a length of 3–5 μm, which is the same length as that of the Te nanowires, and a diameter of 300–500 nm, which is greater than that of the Te nanowires. The experimental results indicated that volume expansion of the Bi2Te3 nanowires was a result of the interdiffusion of Bi and Te atoms when Bi was alloyed on the surface of the Te nanowires. The morphologies of Bi2Te3 are strongly dependent on the reaction conditions such as the temperature and the type and concentration of the reducing agent. The morphologies, crystalline structure and physical properties of the product were analyzed by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and X-ray photoelectron spectroscopy (XPS). 相似文献
865.
In Hwan Jung Hoyeon Kim Moo‐Jin Park Bongjun Kim Jong‐Hwa Park Eunjae Jeong Han Young Woo Seunghyup Yoo Hong‐Ku Shim 《Journal of polymer science. Part A, Polymer chemistry》2010,48(6):1423-1432
We have synthesized two cyclopentadithiophene (CDT)‐based low bandgap copolymers, poly[(4,4‐bis(2‐ethyl‐hexyl)‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl)‐alt‐(benzo[c][1,2,5]selenadiazole‐4,7‐diyl)] (PCBSe) and poly[(4,4‐bis(2‐ethyl‐hexyl)‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl)‐alt‐(4,7‐dithiophen‐2‐yl‐benzo[c][1,2,5]selenadiazole‐5,5′‐diyl)] (PCT2BSe), for use in photovoltaic applications. Through the internal charge transfer interaction between the electron‐donating CDT unit and the electron‐accepting benzoselenadiazole, we realized exceedingly low bandgap polymers with bandgaps of 1.37–1.46 eV. The UV–vis absorption maxima of PCT2BSe were subjected to larger hypsochromic shifts than those of PCBSe, because of the distorted electron donor–acceptor (D–A) structures of the PCT2BSe backbone. These results were supported by the calculations of the D–A complex using the ab initio Hartree‐Fock method with a split‐valence 6‐31G* basis set. However, PCT2BSe exhibited a better molar absorption coefficient in the visible region, which can lead to more efficient absorption of sunlight. As a result, PCT2BSe blended with [6,6]‐phenyl‐C61‐butyric acid methyl ester (PC61BM) exhibited a better photovoltaic performance than PCBSe because of the larger spectral overlap integral with respect to the solar spectrum. Furthermore, when the polymers were blended with PC71BM, PCT2BSe showed the best performance, with an open circuit voltage of 0.55 V, a short‐circuit current of 6.63 mA/cm2, and a power conversion efficiency of 1.34% under air mass 1.5 global illumination conditions. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1423–1432, 2010 相似文献
866.
867.
MD. Daloar Hossain Le Thi Bao Tran Jong Myung Park Kwon Taek Lim 《Journal of polymer science. Part A, Polymer chemistry》2010,48(22):4958-4964
A new, efficient method for synthesizing stable nanoparticles with poly(ethylene oxide) (PEO) functionalities on the core surface, in which the micellization and crosslinking reactions occur in one pot, has been developed. First, amphiphilic PEO‐b‐PS copolymers were synthesized by reversible addition fragmentation chain transfer (RAFT) radical polymerization of styrene using (PEO)‐based trithiocarbonate as a macro‐RAFT agent. The low molecular weight PEO‐b‐PS copolymer was dissolved in isopropyl alcohol where the block copolymer self‐assembled as core‐shell micelles, and then the core‐shell interface crosslink was performed using divinylbenzene as a crosslinking agent and 2,2′‐azobisisobutyronitrile as an initiator. The design of the amphiphilic RAFT agent is critical for the successful preparation of core‐shell interface crosslinked micellar nanoparticles, because of RAFT functional groups interconnect PEO and polystyrene blocks. The PEO functionality of the nanoparticles surface was confirmed by 1H NMR and FTIR. The size and morphology of the nanoparticles was confirmed by scanning electron microscopy, transmission electron microscopy, and dynamic laser light scattering analysis. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
868.
869.
Junhan Cho Min Su Park Jin Hyun Choi Byung Chul Ji Sung Soo Han Won Seok Lyoo 《Journal of Polymer Science.Polymer Physics》2001,39(15):1778-1783
A novel blend system was prepared by blending organosoluble nitro‐substituted polybenzimidazole (NO2‐PBI) and polyetherimide (PEI) in a cosolvent at a moderate condition. It was shown that the NO2‐PBI/PEI blends not only possess tractable processability owing to the enhanced solubility of NO2‐PBI but also retain the desirable features of unmodified PBI/PEI blends. Apparent miscibility in the blends was observed and attributed to hydrogen‐bonding interactions between N? H groups in NO2‐PBI and carbonyl groups in PEI. It was revealed that the NO2‐PBI/PEI blends phase‐separate upon heating above the glass‐transition temperatures. The observed mixing of NO2‐PBI and PEI in a molecular level, although sustainable only in the glassy region, was shown to lend synergy effects to the physical properties of the blends. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 1778–1783, 2001 相似文献
870.