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121.
The K-shell X-ray fluorescence cross sections are determined experimentally for 10 elements such as Pb, Hg, Ir, W, Lu, Tm,
Dy, Tb, Gd and Nd at excitation energy of 661.6 keV associated with γ-rays of 137Cs radioisotope. The technique employed involves the measurement of total intensity of fluorescent K X-rays that follow the
photoeffect absorption of a known flux of γ-rays using a well type Nal(Tl) detector. The obtained results are compared with the available theoretical values and other
measured values. 相似文献
122.
123.
Spectrally Adjustable Picosecond Dye Laser Pulses Generated with Nanosecond Nitrogen Lasers 总被引:2,自引:0,他引:2
Nguyen Dai Hung Pham Long Dinh Van Trung Nguyen Van Tien Le Hoang Hai Nguyen Ha 《Chinese Journal of Lasers》1995,4(5):385-392
SpectrallyAdjustablePicosecondDyeLaserPulsesGeneratedwithNanosecondNitrogenLasersNguyenDaiHung;PhamLong;DinhVanTrung;NguyenVa... 相似文献
124.
Thi Bang Tam Dao Kim Ngoc Pham Yi-Lung Cheng Sang Sub Kim Bach Thang Phan 《Current Applied Physics》2014,14(12):1707-1712
The as-deposited WO3 thin films were post-annealed at different temperatures (300 °C and 600 °C) in air to investigate a correlation between crystallinity and switching behavior of WO3 thin films. Associating the results of XRD, FTIR, XPS and FESEM measurements, the annealing-caused crystallinity change contributes to the variation of the switching behaviors of the WO3 thin films. The as-deposited WO3 films with low crystalline structure are preferred for random Ag conducting path, resulting in large switching ratio but fluctuating I–V hysteresis, whereas the annealed WO3 films with crystallized compact structure limits Ag conducting path, favoring the stable I–V hysteresis but small switching ratio. It is therefore concluded that electrochemical redox reaction-controlled resistance switching depends not only on electrode materials (inert and reactive electrodes) but also on crystallinity of host oxide. 相似文献
125.
Simultaneous analyses of inclusive and semi-inclusive reactionns in neutrino-nucleon collisions and elastic neutrino-proton scattering uniquely determine the neutral-current couplings between neutrinos and hadrons up to a two-fold “vector-axial-vector ambiguity”. One of the preferred solutions coincides with the Salam-Weinberg model within errors while the other solution, also compatible with SU(2) ? U(1) models with the simplest Higgs mechanism, may be helpful in understanding the bismuth puzzle. 相似文献
126.
Anionic polymerization of methyl methacrylate in THF and toluene at ?70° was studied by means of i.r. spectroscopy. The reaction mixtures show characteristic absorption at 1600–1750 cm?1 caused by the stretching vibrations of the propagating centre as well as by the groups obtained in side reactions (metal splitting, addition to a carbonyl group, cyclization). Sec-butyllithium is more effective in THF than n-butyllithium, ethyllithium and fluorenyllithium. When polymerizing in toluene, small amounts of a donor (THF or HMPT) cause formation of active centres similar to those in pure THF. The “living” ends of oligo-MMA form 1:1 complexes with electron acceptors such as trialkylaluminium and triethylboron. 相似文献
127.
Dao Pham Kim Gaidadin A. N. Gorkovenko D. A. Navrotskiy V. A. 《Russian Journal of Applied Chemistry》2018,91(2):320-324
Russian Journal of Applied Chemistry - Coagulation of natural rubber and polyvinyl chloride latices with poly(diallyldimethylammonium chloride) was studied. The influence exerted on coagulation of... 相似文献
128.
A continuously monitored system is considered, that gradually and stochastically deteriorates according to a bivariate non-decreasing Lévy process. The system is considered as failed as soon as its bivariate deterioration level enters a failure zone, assumed to be an upper set. A preventive maintenance policy is proposed, which involves a delayed replacement, triggered by the reaching of some preventive zone for the system deterioration level. The preventive maintenance policy is assessed through a cost function on an infinite horizon time. The cost function is provided in full form, and tools are provided for its numerical computation. The influence of different parameters on the cost function is studied, both from a theoretical and/or numerical point of view. 相似文献
129.
Geometric and electronic structures, vibrational properties, and relative stabilities of niobium clusters Nb(n), n = 7-12, are studied using both DFT (BPW91 and M06 functionals) and CCSD(T) calculations with the cc-pVnZ-PP basis set. In each cluster, various lower-lying states are very close in energy in such a way that the ground state cannot be unambiguously established by DFT computations. Nb clusters tend to prefer the lowest possible spin state as the ground state, except for Nb(12) ((3)A(g)). The optimal structure of the cluster at a certain size does not simply grow from that of the smaller one by adding an atom randomly. Instead, the Nb clusters prefer a close-packed growth behavior. Nb(10) has a spherically aromatic character, high chemical hardness and large HOMO-LUMO gap. Electron affinities, ionization energies, binding energy per atom, and the stepwise dissociation energies are evaluated. Energetic properties exhibit odd-even oscillations. Comparison with experimental values shows that both BPW91 and M06 functionals are reliable in predicting the EA and IE values, but the BPW91 is deficient in predicting the binding and dissociation energies. We re-examine in particular the experimental far IR spectra previously recorded using the IR-MPD and free electron laser spectrometric techniques and propose novel assignments for Nb(7) and Nb(9) systems. The IR spectra of the anions are also predicted. 相似文献
130.
In the copolymerization of vinyl acetate (A) with either vinyl chloride (C) or vinylidene chloride (V), an internal transfer (backbiting) reaction—of the C- or V-ended radi-cals on an antepenultimate A unit—is proposed to be responsible for the deviation of the copolymerization kinetics from the Lewis and Mayo theory. The deviations disappear if A is replaced by isopropenylacetate [Ip], Then one gets, for the Ip -C copolymerization. rI p =0.35 and :rc=2.4, and for I -V copolymerization, rI p=0.13 and rv=5.9. The internal transfer reaction causes the formation of branches which may be evidenced by NMR analysis of constant composition suspension A-C copolymers. A kinetic scheme is proposed and the corresponding reactivity ratios derived rA=0.29, rc=1.60, r=0.3 (radical resulting from the transfer reaction), and kT=1500 (rate constant of the transfer reaction at 50°C). The distribution of branches is calculated together with the sequence distribution functions for the .A. or Cunits. 相似文献