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21.
Churchard AJ Banach E Borgschulte A Caputo R Chen JC Clary D Fijalkowski KJ Geerlings H Genova RV Grochala W Jaroń T Juanes-Marcos JC Kasemo B Kroes GJ Ljubić I Naujoks N Nørskov JK Olsen RA Pendolino F Remhof A Románszki L Tekin A Vegge T Zäch M Züttel A 《Physical chemistry chemical physics : PCCP》2011,13(38):16955-16972
The widespread adoption of hydrogen as an energy carrier could bring significant benefits, but only if a number of currently intractable problems can be overcome. Not the least of these is the problem of storage, particularly when aimed at use onboard light-vehicles. The aim of this overview is to look in depth at a number of areas linked by the recently concluded HYDROGEN research network, representing an intentionally multi-faceted selection with the goal of advancing the field on a number of fronts simultaneously. For the general reader we provide a concise outline of the main approaches to storing hydrogen before moving on to detailed reviews of recent research in the solid chemical storage of hydrogen, and so provide an entry point for the interested reader on these diverse topics. The subjects covered include: the mechanisms of Ti catalysis in alanates; the kinetics of the borohydrides and the resulting limitations; novel transition metal catalysts for use with complex hydrides; less common borohydrides; protic-hydridic stores; metal ammines and novel approaches to nano-confined metal hydrides. 相似文献
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Fijalkowski KJ Genova RV Filinchuk Y Budzianowski A Derzsi M Jaroń T Leszczyński PJ Grochala W 《Dalton transactions (Cambridge, England : 2003)》2011,40(17):4407-4413
We describe the successful synthesis of the first mixed-cation (pseudoternary) amidoborane, Na[Li(NH(2)BH(3))(2)], with theoretical hydrogen capacity of 11.1 wt%. Na[Li(NH(2)BH(3))(2)] crystallizes triclinic (P1) with a = 5.0197(4) ?, b = 7.1203(7) ?, c = 8.9198(9) ?, α = 103.003(6)°, β = 102.200(5)°, γ = 103.575(5)°, and V = 289.98(5) ?(3) (Z = 2), as additionally confirmed by Density Functional Theory calculations. Its crystal structure is topologically different from those of its orthorhombic LiNH(2)BH(3) and NaNH(2)BH(3) constituents, with distinctly different coordination spheres of Li (3 N atoms and 1 hydride anion) and Na (6 hydride anions). Na[Li(NH(2)BH(3))(2)], which may be viewed as a product of a Lewis acid (LiNH(2)BH(3))/Lewis base (NaNH(2)BH(3)) reaction, is an important candidate for a novel lightweight hydrogen storage material. The title material decomposes at low temperature (with onset at 75 °C, 6.0% mass loss up to 110 °C, and an additional 3.0% up to 200 °C) while evolving hydrogen contaminated with ammonia. 相似文献
24.
V. P. Antonovich I. V. Stoyanova N. A. Chivireva E. V. Timukhin V. F. Zinchenko N. P. Efryushina 《Journal of Analytical Chemistry》2007,62(3):238-244
Diffuse reflectance spectroscopy in the UV, visible, and near-IR regions is found to allow the detection and identification of lanthanide oxides, fluorides, sulfides, and sulfofluorides without decomposing and dissolving samples. A nondestructive method for the detection and quantitative determination of more than 1 wt % of Eu(II) in the corresponding fluorides is proposed. 相似文献
25.
Polyelectrolyte microcapsules composed by using the LbL technique on stabilized RBC as templates were coated with up to ten layer pairs of trypsin/PSS or trypsin/alginate. The trypsin layer growth was confirmed by particle electrophoresis, confocal laser scanning microscopy, flow cytometry, and protein determination according to Lowry. In the coating series with trypsin/PSS, the amount of immobilized enzyme was larger than that with trypsin/alginate. The enzyme immobilization led to activity reduction of up to 90% compared to that of the same enzyme amount in the solution. No significant differences between the activities of trypsin immobilized in combination with PSS and with alginate were found. 相似文献
26.
The oxidation of ascorbic acid (AA) and dopamine (DA) is studied on non-modified and copper crystal-modified poly(3,4-ethylenedioxythiophene) (PEDOT)-coated electrodes. Both oxidation reactions are studied for different thickness of the polymer layers. For several microns thick PEDOT layers both PEDOT and Cu-modified PEDOT show the largest currents. A stable voltammetric response for AA oxidation is observed together with a linear dependence of the peak currents on concentration in the 0.3 to 6.0 mM range. For DA oxidation, however, a gradual loss of electroactivity is found with increasing number of voltammetric scans and concentration. This problem is overcome by using thinner (<1 µm) polymer layers. In the presence of both AA and DA, the Cu-modified PEDOT-coated electrodes provide better selectivity with respect to DA in comparison to non-modified PEDOT due to partial suppression of the AA oxidation currents. Thin PEDOT layers modified with electrodeposited Cu crystals show a stable and sensitive response for DA oxidation in the micromolar concentration range. A linear dependence of the voltammetric peak currents is found in a wide concentration range (from 6 to about 200 µM) of DA in the presence of a large excess (1 mM concentration) of AA. The sensitivity is 0.013 µA?µM-1. 相似文献
27.
D. Kocheva G. Rainovski J. Jolie N. Pietralla A. Blazhev A. Astier R. Altenkirch S. Ansari Th. Braunroth M. L. Cortés A. Dewald F. Diel M. Djongolov C. Fransen K. Gladnishki A. Hennig V. Karayonchev J. M. Keatings E. Kluge J. Litzinger C. Müller-Gatermann P. Petkov M. Rudigier M. Scheck Ph. Scholz P. Spagnoletti M. Spieker C. Stahl R. Stegmann M. Stoyanova P. Thöle N. Warr V. Werner W. Witt D. Wölk K. O. Zell P. Van Isacker V. Yu. Ponomarev 《The European Physical Journal A - Hadrons and Nuclei》2017,53(9):175
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29.
Albena Bachvarova-Nedelcheva Stancho Yordanov Reni Iordanova Irina Stambolova Angelina Stoyanova Nelly Georgieva Veronica Nemska 《Molecules (Basel, Switzerland)》2021,26(13)
TiO2 nanopowders modified by Nd and Sm were prepared using the sol-gel technique. It was found by XRD analysis that the samples containing Sm are amorphous up to 300 °C, while those with Nd preserve a mixed organic-inorganic amorphous structure at higher temperatures (400 °C). The TiO2 (rutile) was not detected up to 700 °C in the presence of both modified oxides. TiO2 (anatase) crystals found at about 400 °C in the Sm-modified sample exhibited an average crystallite size of about 25–30 nm, while doping with Nd resulted in particles of a lower size—5–10 nm. It was established by DTA that organic decomposition is accompanied by significant weight loss occurring in the temperature range 240–350 °C. Photocatalytic tests showed that the samples heated at 500 °C possess photocatalytic activity under UV irradiation toward Malachite green organic dye. Selected compositions exhibited good antimicrobial activity against E. coli K12 and B. subtilis. 相似文献
30.
Yanislav Danchovski Hristo Rasheev Radostina Stoyanova Alia Tadjer 《Molecules (Basel, Switzerland)》2022,27(20)
All-organic Li-ion batteries appear to be a sustainable and safer alternative to the currently-used Li-ion batteries but their application is still limited due to the lack of organic compounds with high redox potentials toward Li+/Li0. Herein, we report a computational design of nickel complexes and coordination polymers that have redox potentials spanning the full voltage range: from the highest, 4.7 V, to the lowest, 0.4 V. The complexes and polymers are modeled by binding low- and high-oxidized Ni ions (i.e., Ni(II) and Ni(IV)) to redox-active para-benzoquinone molecules substituted with carboxyl- and cyano-groups. It is found that both the nickel ions and the quinone-derived ligands are redox-active upon lithiation. The type of Ni coordination also has a bearing on the redox potentials. By combining the complex of Ni(IV) with 2-carboxylato-5-cyano-1,4-benzoquinones as a cathode and Ni(II)-2,5-dicarboxylato-3,6-dicyano-1,4-benzoquinone coordination polymer as an anode, all-organic Li-ion batteries could be assembled, operating at an average voltage exceeding 3.0 V and delivering a capacity of more than 300 mAh/g. 相似文献