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1.
2.
P. K. Kashkarov B. V. Kamenev M. G. Lisachenko O. A. Shalygina V. Yu. Timoshenk M. Schmidt J. Heitmann M. Zacharias 《Physics of the Solid State》2004,46(1):104-108
The photoluminescence spectra and kinetics of both erbium-doped and undoped multilayer structures of quasi-ordered silicon
nanocrystals in a silicon dioxide matrix were studied. It was shown that the optical excitation energy of silicon nanocrystals
2–3 nm in size can be practically completely transferred to Er3+ ions in the oxide surrounding the nanocrystals, with its subsequent radiation at 1.5 μm. Possible reasons for the high excitation
efficiency of the Er3+ ions are discussed, and the conclusion is drawn that the F?rster mechanism is dominant in the energy transfer processes occurring
in these structures.
__________
Translated from Fizika Tverdogo Tela, Vol. 46, No. 1, 2004, pp. 105–109.
Original Russian Text Copyright ? 2004 by Kashkarov, Kamenev, Lisachenko, Shalygina, Timoshenko, Schmidt, Heitmann, Zacharias. 相似文献
3.
H. Zacharias 《Applied Physics A: Materials Science & Processing》1988,47(1):37-54
In this article the application of tunable dye lasers to desorption phenomena is illuminated. These lasers provide radiation continuously tunable from 105 nm in the vacuum ultraviolet to about 10 m in the mid-IR. By employing either laser induced fluorescence (LIF) or resonance enhanced multiphoton ionization (REMPI) spectroscopy almost all diatomic and many polyatomic molecules can be probed with the sensitivity required to detect desorbing molecules under UHV conditions. The spectral resolution of the lasers is sufficiently high that rotational state selectivity is achieved. Recent developments permit in addition the velocity distributions of molecules to be determined with internal quantum state resolution. Therefore very detailed information about the molecular dynamics has been obtained. In most experiments so far reactive recombinations off surfaces have been investigated. In this paper special emphasis will be given to the recombination of hydrogen on copper and palladium surfaces. For these systems very detailed data about the internal state populations at various surface temperatures have been obtained. The rotational cooling previously observed in molecular beam scattering has also been established for desorption. Strong vibrational excitation has been observed, which in the case of desorption from copper may be associated with the recombination dynamics, whereas for desorption of D2 from Pd(100) a molecular precursor state might be responsible. By measuring the velocity distribution in each quantum state, the complete energetics of the desorbing molecules has been determined. Some first experiments on laser induced desorption with state selective detection of the desorbing molecules will also be discussed. Finally, making use of the polarization analysis of the signal, alignment effects in the desorption can be observed, permitting observation of molecular dynamics with a magnifying glass.Heisenberg fellow of the Deutsche Forschungsgemeinschaft 相似文献
4.
The thermal decompositions of-AlF3 · 3H2O, AlF3 · 3.5H2O, AlF3 · 1.5H2O,-AlF3 and hydroxyfluorides of aluminium were investigated. The literature data were complemented with X-ray results. The first stages of decomposition are described. The AlF3 hydrates and hydroxyfluorides were used as model systems in order to interpret the thermal behaviour of -AlF3 in more detail.
Zusammenfassung Die thermische Zersetzung von-AlF3 · 3H2O, AlF3 · 3,5H2O, AlF3 · 1,5H2O,-AlF3 und Hydroxyfluoriden des Aluminiums wurden untersucht und die in der Literatur beschriebenen Ergebnisse durch Röntgenuntersuchungen ergänzt. Die ersten Phasen der Zersetzung werden beschrieben. Die AlF3-Hydrate und Hydroxyfluoride des Aluminiums können als Modellsystem genutzt werden, um das thermische Verhalten von -AlF3 detailliert zu beschreiben.
-AlF3 · 2, AlF3 · 3,52, AlF3 · 1,52,-AlF3 . . . - lF3.相似文献
5.
U. Robra H. Zacharias K. H. Welge 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1990,16(3):175-188
The dynamics of the photodissociation of NO2 into NO(X 2ΠΩ″, ν″=0,J″)+O(3 P 0,1,2) is investigated near the thermodynamic threshold. Cooling the internal degrees of freedom by a supersonic beam expansion provides a nearly complete quantum state selection prior to the predissociation. Measurements of the wavelength dependent dissociation yield into specific product quantum states are reported. At certain wavelengths Λ″ doublet resolved rotational population distributions of the fragments are obtained. Up to an excess energy ofE exc=121 cm?1 about 42% of this energy is partitioned into the rotation of the NO molecules, and correspondingly 58% into the translational degree of freedom. The role of electronic and total parity is discussed. 相似文献
6.
Korupoju SR Mangayarkarasi N Zacharias PS Mizuthani J Nishihara H 《Inorganic chemistry》2002,41(16):4099-4101
New homo trinuclear Zn(II) complexes [Zn(3)L(1)(micro-OAc)](ClO(4))(2).3CHCl(3).H(2)O, 1, and [Zn(3)L(1)(micro-OAc)].ClO(4).PF(6).5CH(3)OH.H(2)O, 2, and hetero trinuclear complex [Zn(2)CuL(1)(micro-OAc)](ClO(4))(2).3CHCl(3).H(2)O,3, of optically active hexaaza triphenolic macrocycle H(3)L(1) were synthesized and crystallographically characterized. The cation [Zn(3)L(1)(micro-OAc)](+) structure of 1 and 2 closely resembles the trinuclear Zn(II) active site of P1 nuclease. The distorted tetrahedral geometry of Zn3 was successfully reproduced at Cu1 in complex 3. The complexes 2 and 3 cleave CT DNA at 37 and 50 degrees C. 相似文献
7.
T. Hoger D. Grimmer H. Zacharias 《Applied Physics A: Materials Science & Processing》2007,88(3):449-458
The desorption of NO from a well-characterized, epitaxially grown semiconducting C60 surface is reported. Two different channels are identified in the laser desorption. Both channels yield a comparably high
desorption cross section of σ1=7.0×10-17 cm2 and σ2=5.5×10-17 cm2 for the first and second channel, respectively. The laser desorbed NO molecules are detected with rovibrational state selectivity
by (1+1) REMPI in the -bands. In the first channel the desorbing molecules are highly excited with an average kinetic energy of 〈Ekin〉=174 meV. The rotational population distribution can be fitted by a rotational temperature of Trot=800 K. A rotational–translational coupling is observed, with velocities ranging from 1000 m/s for low to 1300 m/s for high
rotational states. The vibrationally excited population is estimated to be less than 1% of the ground state. The second channel
yields less excited molecules and an almost Boltzmann distributed rotational population with a temperature of Trot=280 K. The apparent velocity distribution derived from the pump-probe delay yields molecules much too slow to be explained
by even a thermal desorption. This desorption is probably caused by a long-lived electronic excitation in the substrate for
which a lifetime of τ≈160 μs is estimated.
PACS 42.62.Fi; 34.50.Dy; 68.49.Df; 68.43.Tj; 79.20.La 相似文献
8.
9.
Joachim Zacharias 《Proceedings of the American Mathematical Society》2006,134(7):1909-1916
Recently J.Roe considered the question of whether for a discrete group the reduced group -algebra is the fixed point algebra of Ad acting on the uniform Roe algebra . is said to have the invariant translation approximation property in this case. We consider a slight generalization of this property which, for exact , is equivalent to the operator space approximation property of . We also give a new characterization of exactness and a short proof of the equivalence of exactness of and exactness of for discrete groups.
10.
Martin Zacharias 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(18):6028-6033
Sac7d is a small, thermostable protein that induces large helical deformations in DNA upon association. Starting from multiple initial placements of the unbound Sac7d structure relative to a B‐DNA oligonucleotide, molecular dynamics (MD) simulations were employed to directly follow several successful binding events at atomic resolution that resulted in structures in close agreement with the native complex geometry. The final native complex formed rapidly within tenths of nanoseconds and included simultaneous large‐scale kinking, groove opening, twisting, and intercalation in the target DNA. The simulations indicate that the complex formation process involves initial non‐native contacts that helped in reaching the final bound state, with residues intercalated at the center of the kinked DNA. It was also possible to identify several long‐lived trapped intermediate states of the binding process and to follow sliding processes of Sac7d along the DNA minor groove. 相似文献