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排序方式: 共有8196条查询结果,搜索用时 15 毫秒
961.
Antoine Bonnefont Franoise Argoul Martin Z. Bazant 《Journal of Electroanalytical Chemistry》2001,500(1-2)
We investigate the subtle effects of the diffuse charged layer on interfacial kinetics by solving the governing equations for ion transport (Nernst–Planck) with realistic boundary conditions representing reaction kinetics (Butler–Volmer) and compact-layer capacitance (Stern) in the asymptotic limit =λD/L→0, where λD is the Debye screening length and L is the distance between the working and counter electrodes. Using the methods of singular perturbation theory, we derive the leading-order steady-state response to a nonzero applied current in the case of the oxidation of a neutral species into cations, without any supporting electrolyte. In certain parameter regimes, the theory predicts a reaction-limited current smaller than the classical diffusion-limited current; this over potential effect is not due to ohmic drop effects in the bulk of the cell but rather to antagonist processes involved in the surface charge transfer and diffuse layer charging respectively. We demonstrate that the charging of diffuse charge, since it is intimately coupled to the surface reaction and cannot be considered independently, plays a fundamental role in nonequilibrium surface reactions when the transport of one of the reacting species is coupled to the total interfacial response of the compact and diffuse layers. 相似文献
962.
963.
964.
Aneta Slodczyk Philippe Colomban Daniel Lamago Marie-Helene Limage François Romain Stephanie Willemin Beatrice Sala 《Ionics》2008,14(3):215-222
H+-containing lanthanide-doped perovskites A(Ba, Sr etc.)B(Zr, Ce, Ti etc.)O3 are potential ceramic membranes for fuel cell and medium temperature water electrolysis (300–800 °C). The comparison studies
of the hydrated and non-hydrated Yb-doped BaZrO3 and SrZrO3 were performed by thermal expansion, medium–high temperature neutron and room-temperature high-pressure Raman scattering.
Neutron diffraction and elastic/quasi-elastic studies carried out for BaZrO3 ceramic show the presence of the protons, their successive diffusion above ∼600 °C, and then their departure above 750 °C
(under vacuum). Phase transitions and their modification by proton insertion are discussed. A high-pressure Raman study of
SrZrO3 performed at room temperature in the diamond anvil cell reveals the presence of two pressure-induced phase transitions at
about 5 and 22 GPa and confirms that proton insertion modifies the phase transition sequences.
Paper presented at the 11th EuroConference on the Science and Technology of Ionics, Batz-sur-Mer, Sept. 9–15, 2007. 相似文献
965.
966.
T. Çuçi J. Thereska N. Dhamo E. Plasari 《Journal of Radioanalytical and Nuclear Chemistry》1989,136(6):449-453
An experiment on rabbits was carried out with the aim to check results obtained formerly with the help of the neutron activation analysis indicating that Na+ ions can be /by contrast to K+ ions/ only very slowly removed from the bone tissue by extraction with water. The data resulting from a radiotracer experiment with22Na are in a good agreement with the above mentioned results. 相似文献
967.
François Labourie 《Inventiones Mathematicae》1987,90(1):115-138
Sans résumé 相似文献
968.
Nadeem ur Rehman Öznur Gölbaşı Emine Koç 《Rendiconti del Circolo Matematico di Palermo》1938,62(2):245-251
Let \((R,*)\) be a \(2\)-torsion free \(*\)-prime ring with involution \(*\), \(L\ne \{0\}\) be a \(*\)-Lie ideal of \(R\). An additive mapping \(d:R\rightarrow R\) is called an \((\alpha ,\beta )\)-derivation of \(R\) such that \(d(xy)=d(x)\alpha (y)+\beta (x)d(y)\). In the present paper, we shall show that when \(L\) satisfies any of several identities involving \(d\), then \(L\) is central. 相似文献
969.
Constructible motivic functions and motivic integration 总被引:1,自引:0,他引:1
970.
Phthalocyanines with four naphthyl-malonic ester groups on the periphery were synthesized by cyclotetramerization of 4-(1,1-dicarbethoxy-2-(1-naphthyl)-ethyl)-phthalonitrile.
The new compounds were characterized by spectroscopic methods. The electronic spectra exhibit intense π–π* transitions from
the naphthyl moiety together with the characteristic Q and B bands of the phthalocyanine core. The electrochemical properties
of the 2,9,17,23-tetra-(1,1-(dicarbethoxy)-2-(1-naphthyl)-ethyl) phthalocyaninato copper(II) complex were studied by cyclic
voltammetry. 相似文献