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81.
Godelitsas A Charistos D Tsipis A Tsipis C Filippidis A Triantafyllidis C Manos G Siapkas D 《Chemistry (Weinheim an der Bergstrasse, Germany)》2001,7(17):3705-3721
Nickel-loaded HEU-type zeolite crystals have been obtained by well-known synthetic procedures and characterised by X-ray fluorescence (XRF), scanning-electron microscopy/ energy-dispersive spectroscopy (SEM-EDS), FT-IR, diffuse reflectance UV/ Vis spectroscopy (DR(UV/Vis)S) and X-ray photoelectron spectroscopy (XPS) measurements as non-homoionic and non-stoichiometric substances containing exchangeable hydrated Ni2+ ions in the micropores and nickel hydroxide phases supported on the surface. Thermogravimetric analysis/differential gravimetry (TGA/DTG) and differential thermal analysis (DTA) demonstrated that full dehydration below approximately 400 degrees C follows a clearly endothermic process, whereas at higher temperatures the zeolite is amorphised and finally partially recrystallised to Ni(Al,Si) oxides, detected by powder X-ray powder diffraction (XRD). The solid acidity of NiHEU, initially determined by temperature-programmed desorption (TPD) of ammonia to be 8.93 mgg(-1) NH3, is attributed to the weak acid sites (fundamentally Lewis sites) resolved at approximately 183 degrees C, and to the strong acid sites (essentially Br?nsted sites) resolved at approximately 461 degrees C in the TPD pattern. A more sophisticated study based on in situ/ex situ FT-IR with in situ/ex situ 27Al MAS NMR and pyridine (Py) as a probe molecule, revealed that the Lewis acid sites can be attributed primarily to Ni2+ ions, whereas the Br?nsted ones can probably be associated with the surface-supported nickel hydroxide phases. The spectroscopic measurements in conjunction with powder XRD and 29Si MAS NMR data strongly suggest that distorted Al tetrahedra are formed during the dehydration process and Py chemisorption/complexation (NiHEU-Py), whereas the crystal structure is remarkably well preserved in the rehydrated material (NiHEU-Py/R). The structural, electronic, energetic and spectroscopic properties of all possible nickel(II) aqua and dihydroxy complexes absorbed in the zeolite micropores or supported on the zeolite surface were studied theoretically by density functional theory (DFT). The computed proton affinity, found to be in the range 182.0-210.0 kcalmol(-1), increases with increasing coordination number of the aqua and dihydroxy nickel(II) complexes. 相似文献
82.
Ekaterina V. Tsipis Vladislav V. Kharton Jorge R. Frade Pedro Núñez 《Journal of Solid State Electrochemistry》2005,9(8):547-557
The total conductivity of oxygen-hyperstoichiometric YBaCo4O7+ is predominantly p-type electronic at oxygen partial pressures from 5×104 Pa down to the phase decomposition limit, 10–11–10–4 Pa at 973–1223 K. The ion transference numbers, determined by the oxygen permeation and faradaic efficiency measurements at 1073–1223 K, vary in the range 3×10–5–2×10–4 and increase with temperature. The oxygen permeability of YBaCo4O7+ ceramics, with overall level similar to that of K2NiF4-type cuprates, is mainly limited by the bulk ionic conduction. Heating above 1050–1100 K and redox processes under oxidizing conditions lead to a first-order transition accompanied with extensive oxygen losses from the lattice, resulting in decreasing total oxygen content from 8.5 down to approximately seven atoms per unit formula. Except for the variations associated with this transition, the electron–hole conductivity and Seebeck coefficient are essentially p(O2)-independent within the phase stability limits. The use of different synthesis methods, namely the standard ceramic technique and the glycine–nitrate process, has no significant effect on the properties of YBaCo4O7+ ceramics. The thermal expansion coefficients averaged at 600–1100 K in air are (7.3–7.6)×10–6 K–1. Porous YBaCo4O7-based cathodes show a very high electrochemical activity in contact with LaGaO3-based solid electrolyte at 873–1073 K. 相似文献
83.
Zircon-type Ce1−xAxVO4+δ (A=Ca, Sr; x=0-0.2) are stable in air up to approximately 1300 K, whilst further heating or reducing oxygen partial pressure leads to formation of A-site deficient zircon and CeO2−δ phases. The stability boundaries of Ce1−xAxVO4+δ are comparable to those of vanadium dioxide and calcium orthovanadate. At oxygen pressures lower than 10−15 atm, perovskite-type CeVO3−δ is formed. The oxygen ion transference numbers of Ce1−xAxVO4+δ, determined by faradaic efficiency measurements in air, vary in the range from 2×10−4 to 6×10−3 at 973-1223 K, increasing with temperature. The oxygen ionic conductivity has activation energy of 87-112 kJ/mol and is essentially independent of A-site dopant content. Contrary to the ionic transport, p-type electronic conductivity and Seebeck coefficient of Ce1−xAxVO4+δ are influenced by the divalent cation concentration. The average thermal expansion coefficients of Ce1−xAxVO4+δ, calculated from high-temperature XRD and dilatometric data in air, are (4.7-6.1)×10−6 K−1. 相似文献
84.
Aitala EM Amato S Anjos JC Appel JA Ashery D Banerjee S Bediaga I Blaylock G Bracker SB Burchat PR Burnstein RA Carter T Carvalho HS Costa I Cremaldi LM Darling C Denisenko K Fernandez A Gagnon P Gerzon S Gobel C Gounder K Granite D Halling AM Herrera G Hurvits G James C Kasper PA Kondakis N Kwan S Langs DC Leslie J Lichtenstadt J Lundberg B Manacero A MayTal-Beck S Meadows B de Mello Neto JR Milburn RH de Miranda JM Napier A Nguyen A d'Oliveira AB O'Shaughnessy K Peng KC Perera LP Purohit MV 《Physical review letters》1996,76(3):364-367
85.
Bizau J Esteva J Cubaynes D Wuilleumier FJ Blancard C La Fontaine AC Couillaud C Lachkar J Marmoret R Remond C Bruneau J Hitz D Ludwig P Delaunay M 《Physical review letters》2000,84(3):435-438
Photoionization of Xe4+ to Xe7+ ions was studied by combining an electron cyclotron resonance ion source with synchrotron radiation. Multiconfiguration Dirac-Fock calculations were performed to interpret the data. Many autoionization lines were measured and identified, resulting from excitation of a 4d electron into nf and np orbitals followed by Auger decay of the excited states. Continuum photoionization is negligible for the higher members of the isonuclear series. 相似文献
86.
87.
I. E. Kuritsyna V. V. Sinitsyn Yu. S. Fedotov S. I. Bredikhin E. V. Tsipis V. V. Kharton 《Russian Journal of Electrochemistry》2014,50(8):713-718
Studies of oxygen diffusion, interphase exchange, specific electric conductivity, and thermal expansion showed that perovskite-like Sr0.7Ce0.3MnO3 ? δ (SCMO) as a potential cathode material for solid oxide fuel cells (SOFCs) has considerable advantages over the conventional materials based on lanthanum-strontium manganites. To prevent the interactions of SCMO with solid electrolyte membranes of stabilized zirconia and lanthanum gallate, it is necessary to deposit protective layers of solid solutions based on cerium oxide, which do not form new phases in contact with SCMO and electrolytes. The trials of model SOFCs with porous SCMO-based cathodes demonstrated satisfactory electrochemical and endurance characteristics of these electrodes. 相似文献
88.
E.V. Tsipis V.V. Kharton E.N. Naumovich 《Journal of Physics and Chemistry of Solids》2006,67(8):1882-1887
The redox behavior of perovskite-type La0.90Sr0.10Al0.85−xFexMg0.15O3−δ (x=0.20-0.40) mixed conductors was analyzed by the Mössbauer spectroscopy and measurements of the total conductivity and Seebeck coefficient in the oxygen partial pressure range from 10−20 to 0.5 atm at 1023-1223 K. The results combined with oxygen-ion transference numbers determined by the faradaic efficiency technique in air, were used to calculate defect concentrations, mobilities, and partial ionic and p- and n-type electronic conductivities as a function of oxygen pressure. The redox and transport processes can be adequately described in terms of oxygen intercalation and iron disproportionation reactions, with the thermodynamic functions independent of defect concentrations. No essential delocalization of the electronic charge carriers was found. The oxygen non-stoichiometry values estimated from the conductivity vs. p(O2) dependencies, coincide with those evaluated from the Mössbauer spectra. 相似文献
89.
S. K. Poznyak V. V. Kharton J. R. Frade A. A. Yaremchenko E. V. Tsipis S. O. Yakovlev I. P. Marozau 《Journal of Solid State Electrochemistry》2008,12(1):15-30
The behavior of dense ceramic anodes made of perovskite-type (x = 0.30–0.70; y = 0–0.05; z = 0–0.20) and K2NiF4-type (Me = Co, Cu; x = 0–0.20) indicates significant influence of metal hydroxide formation at the electrode surface on the oxygen evolution reaction
(OER) kinetics in alkaline solutions. The overpotential of cobaltite electrodes was found to decrease with time, while cyclic
voltammetry shows the appearance of redox peaks characteristic of Co(OH)2/CoOOH. This is accompanied with increasing effective capacitance estimated from the impedance spectroscopy data, because
of roughening of the ceramic surface. The steady-state polarization curves of in the OER range, including the Tafel slope, are very similar to those of model Co(OH)2–La(OH)3 composite films where the introduction of lanthanum hydroxide leads to decreasing electrochemical activity. La2NiO4-based anodes exhibit a low electrochemical performance and poor stability. The effects of oxygen nonstoichiometry of the
perovskite-related phases are rather negligible at high overpotentials but become significant when the polarization decreases,
a result of increasing role of oxygen intercalation processes. The maximum electrocatalytic activity to OER was observed for
A-site-deficient , where the lanthanum content is relatively low and the Co4+ concentration determined by thermogravimetric analysis is highest compared to other cobaltites. Applying microporous layers
made of template-synthesized nanocrystalline leads to an improved anode performance, although the effects of microstructure and thickness are modest, suggesting a narrow
electrochemical reaction zone. Further enhancement of the OER kinetics can be achieved by electrodeposition of cobalt hydroxide-
and nickel hydroxide-based films.
Dedicated to Professor Dr. Yakov I. Tur’yan on the occasion of his 85th birthday. 相似文献
90.
Forniés J Ibáñez S Lalinde E Martín A Moreno MT Tsipis AC 《Dalton transactions (Cambridge, England : 2003)》2012,41(12):3439-3451
The reaction between (NBu(4))[Pt(bzq)(C(6)F(5))(2)] (1, bzq = 7,8-benzoquinolate) and AgClO(4) in a 1 : 1 molar ratio, in acetone, gives the polymer [{Pt(bzq)(C(6)F(5))(2)}Ag](n) (2). The reaction of 2 with equimolecular amounts of PPh(3) and SC(4)H(8) (tht) produces the bimetallic complexes [{Pt(bzq)(C(6)F(5))(2)}AgL] (L = PPh(3) (3), tht (4)). For L = py, decomposition takes place and [Pt(bzq)(C(6)F(5))py] (5) is obtained. All these complexes have been characterized by X-ray diffraction. The most interesting features of complexes 2-4 is the presence of Pt-Ag bonds, with Pt-Ag distances of ca. 2.75 ?. Besides, the silver centres establish short η(1) bonding interactions with the C(ipso) of the bzq ligands, with distances Ag-C of ca. 2.45 ?. Complex 2 is a one-dimensional infinite chain in which the fragments "Pt(bzq)(C(6)F(5))(2)(-)" and Ag(+) alternate. On the other hand, complexes 1 and 3-5 show intermolecular pairing through π···π interactions between the aromatic rings of the bzq ligand, having interplanar separations of ca. 3.5 ?. Complex 2 dissolves in donor solvents (acetone, THF) as discrete bimetallic solvated fragments [{Pt(bzq)(C(6)F(5))(2)}AgS(n)] (S = solvent), similar to complexes 3 and 4. The persistence of the Pt-Ag bond in 2-4, supported by multinuclear NMR spectroscopy, causes a significant blue-shift in the lowest-lying absorption in relation to 1. This fact is attributed (TD-DFT) to a remarkable modification of the orbitals contributing to the HOMO, which changes the character of the transition from (1)LC/(1)MLCT in 1 to admixture (1)L'LCT/(1)MLCT in the bimetallic complexes. The low energy feature (490-530 nm) of 2 in solid state is attributed to CT from the Pt fragments to the Ag centers. Complexes 2-4 are only emissive in rigid media (solid and glasses). In the solid state, the metallic chain 2 exhibits a bright orange emission (560 nm, 298 K; 590 nm, 77 K), assigned to an excited state involving charge transfer from the platinum fragment with a remarkable contribution of C(6)F(5) (Ar(f)) rings to the Pt-Ag bond ((3)LMM'CT/(3)L'M'CT). However, 3 and 4 exhibit in solid state at 298 K a vibronic band, which is clearly resolved in two close non-equilibrated bands at 77 K in 3, tentatively ascribed to a mixture of (3)MLCT/(3)L'LCT transitions modified by the formation of the Pt-Ag bond. In glassy solution (77 K) 2-4 display a vibronic emission ascribed primarily to (3)LC character. 相似文献