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1.
Инвентарный номер: нет.
   
   A 10


   
    A Novel Complex Cobalt Gallium Oxide Ca2Co0.8Ga1.2O4.8: Synthesis and High-Temperature Electron Transport Properties [] = A Novel Complex Cobalt Gallium Oxide Ca2Co0.8Ga1.2O4.8: Synthesis and High-Temperature Electron Transport Properties / S. Ya. Istomin, E. V. Antipov, G. Svensson, J. P. Attfield, V. L. Kozhevnikov, I. A. Leonidov, M. V. Patrakeev, E. B. Mitberg // Journal of Solid State Chemistry. - 2002. - V. 167, N 1. - С. 196-202 . - ISSN 0022-4596
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
СЛОЖНЫЕ ОКСИДЫ -- ОКСИДЫ СЛОЖНЫЕ -- ЭЛЕКТРОНЫ -- ДИФРАКЦИЯ -- ЭЛЕКТРОННЫЕ СВОЙСТВА -- СВОЙСТВА ЭЛЕКТРОННЫЕ -- ПОРОШКИ -- ОКСИД КОБАЛЬТА -- ОКСИД ГАЛЛИЯ -- СИНТЕЗ -- ПРОВОДИМОСТЬ -- ВЫСОКОТЕМПЕРАТУРНЫЕ СВОЙСТВА -- СВОЙСТВА ВЫСОКОТЕМПЕРАТУРНЫЕ -- ЭЛЕКТРИЧЕСКИЕ СВОЙСТВА -- СВОЙСТВА ЭЛЕКТРИЧЕСКИЕ -- Co -- Ga -- Ga -- КОБАЛЬТ -- ГАЛЛИЙ -- РЕНТГЕНОВСКАЯ ДИФРАКЦИЯ
Аннотация: A new complex oxide with the cation ratio Ca:Co:Ga = 2:0.8:1.2 has been synthesized in air at 1150oC. The cobalt atoms adopt oxidation states 2+ and 3+ in equal amounts giving an oxygen content corresponding to the composition Ca2Co0.8Ga1.2O4.8. It crystallizes in F-centered cubic structure with a = 15.0558 Angstrom. Conductivity measurements performed at high temperatures revealed that the temperature increase gives a charge disproportionation of Co3+ species resulting in a small concentration of Co4+ species and thus a small p-type conductivity in the oxide. A decrease of the oxygen pressure promotes oxygen depletion from the oxide and a deterioration of the conductivity. The electric properties are interpreted within a small polaron conduction mechanism. An unusually large mobility activation energy of 0.45 eV can be explained by a large spatial separation of cobalt cations in the structure

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2.
Инвентарный номер: нет.
   
   A 90


   
    Atomic structure and ionic conductivity of glassy materials based on silver sulfide / N. V. Melnikova, K. V. Kurochka, O. L. Kheifets, Y. Y. Volkova, N. I. Kadyrova // Bulletin of the Russian Academy of Sciences: Physics. - 2015. - Vol. 79, № 6. - С. 719-722
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ИОННЫЕ ПРОВОДНИКИ -- НАНОТРУБКИ -- ПРОВОДИМОСТЬ
Аннотация: The effect of the composition of glassy ionic conductors AgGe1 + x As1–x S3 and the composites based on these materials containing single-walled carbon nanotubes (CNT) AgGe1+x As1–x (S + CNT)3, on the atomic structure and ionic conductivity is analyzed.

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3.
Инвентарный номер: нет.
   
   N 30


    Naumovich, E. N.
    Defect formation in LaGa(Mg,Ni)O3-delta: A statistical thermodynamic analysis validated by mixed conductivity and magnetic susceptibility measurements [Текст] / E. N. Naumovich, V. V. Kharton, A. A. Yaremchenko, M. V. Patrakeev, D. G. Kellerman, D. I. Logvinovich, V. L. Kozhevnikov // Physical Review B: Condensed Matter and Materials Physics. - 2006. - Vol. 74, № 6. - С. 064105/1-064105/12. - Библиогр. : с. 064105/11 (55 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
МАГНИТНАЯ ВОСПРИИМЧИВОСТЬ -- ПРОВОДИМОСТЬ -- ГАЛЛАТ ЛАНТАНА -- ПЕРОВСКИТЫ
Аннотация: A statistical thermodynamic approach to analyze defect thermodynamics in strongly nonideal solid solutions was proposed and validated by a case study focused on the oxygen intercalation processes in mixed-conducting LaGa0.65Mg0.15Ni0.20O3−delta perovskite. The oxygen nonstoichiometry of Ni-doped lanthanum gallate, measured by coulometric titration and thermogravimetric analysis at 923–1223 K in the oxygen partial pressure range 5 10−5 to 0.9 atm, indicates the coexistence of Ni2+, Ni3+, and Ni4+ oxidation states. The formation of tetravalent nickel was also confirmed by the magnetic susceptibility data at 77–600 K, and by the analysis of p-type electronic conductivity and Seebeck coefficient as function of the oxygen pressure at 1023–1223 K. The oxygen thermodynamics and the partial ionic and hole conductivities are strongly affected by the pointdefect interactions, primarily the Coulombic repulsion between oxygen vacancies and/or electron holes and the vacancy association with Mg2+ cations. These factors can be analyzed by introducing the defect interaction energy in the concentration-dependent part of defect chemical potentials expressed by the discrete Fermi-Dirac distribution, and taking into account the probabilities of local configurations calculated via binomial distributions

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4.
Инвентарный номер: нет.
   
   V 18


    Valeeva, A. A.
    Electrokinetic and Magnetic Properties of Cubic Titanium Monoxide with a Double-Defect Structure / A. A. Valeeva, A. A. Rempel, A. I. Gusev // Doklady Physics. - vol. 47, № 1. - P. 39-43 : ил. - Bibliogr. : p. 43 (15 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
СВОЙСТВА ЭЛЕКТРОКИНЕТИЧЕСКИЕ -- СВОЙСТВА МАГНИТНЫЕ -- МОНООКСИД ТИТАНА -- ПРОВОДИМОСТЬ

\\\\Expert2\\nbo\\Doklady Physics\\2002, V.47, N 1, p. 39-43.pdf
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5.
Инвентарный номер: нет.
   
   E 43


   
    Electron/hole and ion transport in La1-xSrxFeO3-delta [] / M. V. Patrakeev, J. A. Bahteeva, E. B. Mitberg, I. A. Leonidov, V. L. Kozhevnikov, K. R. Poeppelmeier // Journal of Solid State Chemistry. - 2003. - V. 172, N 1. - С. 219-231 . - ISSN 0022-4596
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЭЛЕКТРОННЫЕ ДЫРКИ -- ИОННЫЙ ПЕРЕНОС -- La1-xSrxFeO3-ДЕЛЬТА -- ФЕРРИТЫ ЛАНТАНОСТРОНЦИЕВЫЕ -- КИСЛОРОДНАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ КИСЛОРОДНАЯ -- ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ ЭЛЕКТРОННАЯ -- ЛАНТАН-СТРОНЦИЙ
Аннотация: The conductivity of the entire solid solution La1-xSrxFeO3-delta, where x = 0.2, 0.4, 0.5, 0.7 and 0.9, in the oxygen partial pressure range 10(-19)-0.5 atm and temperatures between 750°C and 950°C is reported. The partial contributions from different charge carriers and the energetic parameters governing transport of charged species reveal that the lanthanum-strontium ferrites can be characterized as mixed, ion-electron conductors in the low oxygen pressure/high oxygen deficiency limit. The partial contributions to conductivity from oxygen ions, electrons and holes increase with strontium content and attain maximal values at x = 0.5. Further increase in doping results in development of oxygen vacancy ordering phenomena and deterioration of conducting properties

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6.
Инвентарный номер: нет.
   
   L 55


    Leonidov, I. A.
    Electronic Conductivity of Sr3 - 3xLa2xvacancyx(VO4)2 Solid Solutions / I. A. Leonidov, O. N. Leonidova, V. K. Slepukhin // Inorganic Materials. - 2000. - Vol. 36, № 1. - P. 72-75 : il. - Bibliogr. : p. 75 (8 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- РАСТВОРЫ ТВЕРДЫЕ -- ВАНАДАТЫ -- СТРОНЦИЙ -- ЛАНТАН
Аннотация: The electronic conductivity of Sr 3 3xLa2x[vacancylx(VO4)2 solid solutions was measured at oxygen pressures from 10 -13 tO 105 Pa and temperatures from 1070 to 1270 K, and their band gap was determined as a function of composition. The activation energy (~2.85 eV) and enthalpies of electron generation (=,4.2 eV) and migration (~-0.75 eV) were determined. A correlation between the band gap and electronic conductivity of the solid solutions was revealed

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7.
Инвентарный номер: нет.
   
   E 43


   
    Electronic structure and chemical bonding in K2V3O8 [Текст] / V. M. Zainullina, V. L. Volkov, N. V. Podvalnaya, A. L. Ivanovskii // Journal of Structural Chemistry. - 2005. - Vol. 46, № 2. - С. 340-342. - Библиогр. : с. 342 (14 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ПОЛИВАНАДАТ КАЛИЯ -- ИОННАЯ ПРОВОДИМОСТЬ
Аннотация: The calculations of the electronic structure of layered polyvanadate K2V3O8 were made employing the spinpolarized tight-binding LMTO method. Calculated magnetic moment for K4V6O16 compound phase equals 1.97 мB. V-O interactions were established to be dominating in the chemical bonding generation in this polyvanadate according to the estimated crystal orbital overlap population. The covalent bonds V(2)-V(2) in V(2)2O7 groups and electron density localization on vanadium atoms in isolated pyramids V(1)O were found.

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8.
Инвентарный номер: нет.
   
   Z 18


    Zainullina, V. M.
    Electronic structure and ionic conductivity in ZrO2, ZrO2-CaO, ZrO2-Y2O3 by the ab initio LMTO-TB supercell approach [] / V. M. Zainullina, V. P. Zhukov, V. M. Zhukovsky // Physics and chemistry of novel materials: 4th Bilateral Russian-German Symposium (Febr. 24-March 1, 1999): Progr. and abstr. - 1999. - С. 2.32
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
СТРУКТУРА ЭЛЕКТРОННАЯ -- ЭЛЕКТРОННАЯ СТРУКТУРА -- ПРОВОДИМОСТЬ ИОННАЯ -- ИОННАЯ ПРОВОДИМОСТЬ -- ЛМТО МЕТОД -- ZrO2 -- Zr -- ЦИРКОНИЙ -- ОКСИД ЦИРКОНИЯ -- ПРОВОДИМОСТЬ -- CaO -- ОКСИД КАЛЬЦИЯ -- Ca -- КАЛЬЦИЙ -- Y2O3 -- ОКСИД ИТТРИЯ -- Y -- ИТТРИЙ

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9.
Инвентарный номер: нет.
   
   K 49


    Kiselev, A. I.
    Estimation of the Effective Electron Mass in Cerium from the Data of Optical Experiment / A. I. Kiselev, V. I. Kononenko // High Temperature (Translation of Teplofizika Vysokikh Temperatur). - 2003. - Vol. 41, № 6. - P. 771-777 : il. - Bibliogr. : p. 777 (16 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЖИДКИЕ РЗМ -- ЦЕРИЙ -- ПРОВОДИМОСТЬ ОПТИЧЕСКАЯ -- ПЛОТНОСТЬ
Аннотация: The form of the dispersion dependence of the optical conductivity of liquid rare earth metals (REM) in the range of photon energies of about 2 eV is defined by the contribution of the maximum of the density of electron states, which emerges during the Bragg scattering of electrons from the first coordination sphere of a melt. It is shown that, for liquid cerium, the experimental dependence of the optical conductivity in this range of photon energies may be described with due regard for the effective electron mass close to the value of 1.37. It is noted that the inclusion of the effective electron mass in the classical Drude equation for the optical conductivity makes it possible to estimate the value of this parameter on the basis of the data of optical experiment

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10.
Инвентарный номер: нет.
   
   F 42


   
    Ferroelectric–Ionic Conductor Phase Transitions in Optical Nonlinear Ca9R(VO4)7 Vanadates / B. I. Lazoryak, A. A. Belik, S. Yu. Stefanovich, V. A. Morozov, A. P. Malakho, O. V. Baryshnikova, I. A. Leonidov, O. N. Leonidova // Doklady Physical Chemistry. - 2002. - vol. 384, № 4-6. - P. 144-148 : il. - Bibliogr. : p. 148 (15 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ФЕРРОЭЛЕКТРИКИ -- ИОННАЯ ПРОВОДИМОСТЬ -- ФАЗОВЫЙ ПЕРЕХОД -- ВАНАДАТЫ

\\\\Expert2\\nbo\\Doklady Physical Chemistry\\2002, V. 384, N 4-6, p.144-148.pdf
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11.
Инвентарный номер: нет.
   
   H 65


   
    High-temperature electrical conductivity and thermopower in nonstoichiometric La1-xSrxCoO3-delta (x = 0.6) [] / E. B. Mitberg, M. V. Patrakeev, I. A. Leonidov, V. L. Kozhevnikov, K. R. Poeppelmeier // Solid State Ionics. - 2000. - V. 130, N 3-4. - С. 325-330. - Библиогр.: 18 назв. . - ISSN 0167-2738
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЭЛЕКТРОПРОВОДНОСТЬ ВЫСОКОТЕМПЕРАТУРНАЯ -- ВЫСОКОТЕМПЕРАТУРНАЯ ЭЛЕКТРОПРОВОДНОСТЬ -- НЕСТЕХИОМЕТРИЯ -- ТЕРМОЭДС -- ЛАНТАН -- СТРОНЦИЙ -- КОБАЛЬТ -- ПРОВОДНИКИ СМЕШАННЫЕ -- СМЕШАННЫЕ ПРОВОДНИКИ -- КОБАЛЬТИТЫ -- ПРОВОДИМОСТЬ ЭЛЕКТРОННАЯ -- ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- La -- Sr -- Co

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12.
Инвентарный номер: нет.
   
   H 65


   
    High-temperature ion transport in La1-xSrxFeO3-delta [] = High-temperature ion transport in La1-xSrxFeO3-delta / Ju. A. Bahteeva, I. A. Leonidov, M. V. Patrakeev, E. B. Mitberg, V. L. Kozhevnikov, K. R. Poeppelmeier // Journal of Solid State Electrochemistry . - 2004. - V. 8, N 9. - С. 578-584 . - ISSN 1432-8488
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ ЭЛЕКТРОННАЯ -- La1-xSrxFeO3-ДЕЛЬТА -- ЛАНТАН-СТРОНЦИЕВЫЕ ФЕРРИТЫ -- ФЕРРИТЫ ЛАНТАН-СТРОНЦИЕВЫЕ -- КИСЛОРОДНАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ КИСЛОРОДНАЯ -- ВАКАНСИИ КИСЛОРОДНЫЕ -- КИСЛОРОДНЫЕ ВАКАНСИИ -- ИОННЫЙ ПЕРЕНОС -- ПЕРЕНОС ИОННЫЙ -- ТВЕРДЫЕ РАСТВОРЫ -- РАСТВОРЫ ТВЕРДЫЕ -- ВЫСОКОТЕМПЕРАТУРНАЯ ХИМИЯ -- ХИМИЯ ВЫСОКОТЕМПЕРАТУРНАЯ
Аннотация: The conductivity of the entire solid solution La1-xSrxFeO3-delta, where x = 0.2, 0.4, 0.5, 0.7 and 0.9, in the oxygen partial pressure range 10(-19) to 0.5 atm and temperatures between 750 and 950 °C is reported. The analysis of the isothermal pressure dependences of the conductivity reveal that the lanthanum-strontium ferrites can be characterized as mixed ion-electron conductors in the low-oxygen pressure/high-oxygen deficiency limit. The partial contribution to conductivity from oxygen ions increases with strontium content and attains a maximal value at x = 0.5. Further increase in doping results in the development of oxygen vacancy ordering phenomena and deterioration of the conducting properties

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13.
Инвентарный номер: нет.
   
   H 99


   
    Interfacial effects in electrochemical cells for oxygen ionic conduction measurements. III. Transference numbers vs. grain-boundary resistivity [] / V. V. Kharton, F. M. B. Marques, E. V. Tsipis, A. P. Viskup, N. P. Vyshatko, M. V. Patrakeev, E. N. Naumovich, J. R. Frade // Solid State Ionics. - 2004. - V. 168, N 1-2. - С. 137-151. - Bibliogr.: p. 151 (35 ref.) . - ISSN 0167-2738
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
СМЕШАННЫЕ ПРОВОДНИКИ -- ПРОВОДНИКИ СМЕШАННЫЕ -- ТВЕРДЫЕ ЭЛЕКТРОЛИТЫ -- ЭЛЕКТРОЛИТЫ ТВЕРДЫЕ -- ПИРОХЛОР -- ЭЛЕКТРОХИМИЧЕСКИЕ ЭЛЕМЕНТЫ -- ЭЛЕМЕНТЫ ЭЛЕКТРОХИМИЧЕСКИЕ -- ИОННАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ ИОННАЯ -- ВЗАИМОДЕЙСТВИЕ МЕЖФАЗНОЕ -- МЕЖФАЗНОЕ ВЗАИМОДЕЙСТВИЕ -- КЕРАМИКА
Аннотация: Resistive grain boundaries may significantly influence transference numbers of oxygen ion-conducting ceramics due to a distinct blocking effect on the ionic transport with respect to the electronic conduction. This may lead to remarkable uncertainties, particularly in the boundary resistance estimates obtained using impedance spectroscopy without a separation of the ionic and electronic contributions, and in the interpretation of transport parameters determined by DC techniques. The role of grain boundaries was examined by the example of "pure" and SiO2-containing pyrochlore ceramics Gd2-xCaxTi2O7-delta (x = 0.05-0.14), studied at 973-1223 K using impedance spectroscopy, faradaic efficiency and e.m.f. methods. The oxygen ion transference numbers of "pure" materials in air vary in the range 0.95-0.98, increasing when temperature decreases. As expected, minor additions of SiO2 result in segregation of siliceous phase and highly resistive grain boundaries.
The total ion transference numbers of silicaenriched ceramics become considerably lower, 0.76-0.89, and increase with increasing temperature due to relatively high activation energy for the boundary resistivity; the bulk transference numbers extracted from the impedance spectroscopy and faradaic efficiency data are similar for all compositions, with and without SiO2 additions. The results, including dependence of the transport properties on oxygen pressure, suggest that a simplified description of the boundaries as a passive transport-limiting barrier is sufficiently adequate

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14.
Инвентарный номер: нет.
   
   I-76


   
    Ion and electron conduction in SrFe1-xScxO3-delta [Text] / M. V. Patrakeev, A. A. Markov, I. A. Leonidov, V. L. Kozhevnikov, V. V. Kharton // Solid State Ionics. - 2006. - Vol. 177, № 19-25. - P.1757-1760. - Bibliogr. : p. 1760 (12 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ИОННАЯ ПРОВОДИМОСТЬ, ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- СТРОНЦИЙ -- ЖЕЛЕЗО -- СКАНДИЙ -- НЕСТЕХИОМЕТРИЯ
Аннотация: The oxygen ion and electron transport in SrFe1-xScxO3-delta (x =0.1–0.3) system at 700–950 -C were studied analyzing the total conductivity dependencies on the oxygen partial pressure, pO2. The conductivity measurements were performed both under reducing conditions (10(-19)<=pO2<=10(-8) atm) comprising the electron-hole equilibrium point, and in oxidizing atmospheres (10(-5)<=pO2<=0.5 atm) which are??characterized by extensive variations of the oxygen content studied by coulometric titration technique. The incorporation of 10% Sc3+ cations into the iron sublattice suppresses transition of the cubic perovskite phase into vacancy-ordered brownmillerite, thus improving ion conduction at temperatures below 850 -C. When scandium content increases, the ion conductivity becomes considerably lower. The hole mobility is thermallyactivated and varies in the range of 0.001 to 0.05 cm(2) V(-1) s(-1), increasing with oxygen concentration and decreasing on Sc doping

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15.
Инвентарный номер: нет.
   
   I-76


   
    Ion-electron transport in strontium ferrites: relationships with structural features and stability [Text] / M. V. Patrakeev, I. A. Leonidov, V. L. Kozhevnikov, V. V. Kharton // Solid State Sciences. - 2004. - Vol. 6, № 9. - P907-913. - Bibliogr. : p. 913 (27 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ФЕРРИТ СТРОНЦИЯ -- НЕСТЕХИОМЕТРИЯ КИСЛОРОДНАЯ -- ПРОВОДИМОСТЬ ИОННАЯ -- ИОННЫЙ ПЕРЕНОС -- ЭЛЕКТРОННЫЙ ТРАНСПОРТ
Аннотация: The total electrical conductivity of strontium ferrites, including intergrowth Sr4Fe6O13+delta, Sr3Fe2O6+delta with a Ruddlesden-Popper??structure, and SrFeO2.5+delta where the cubic perovskite lattice transforms into vacancy-ordered brownmillerite at p(O2) < 10 Pa and??T < 850 .C, was measured at 650.1000 .C in the oxygen partial pressure range 10.15 Pa to 50 kPa. The data were used in order to determine partial ion, p- and n-type electron contributions in the vicinity of electron.hole equilibrium point. The ferrites with brownmillerite and Ruddlesden-Popper structures exhibit substantial ion transport due to thermally-activated disordering of oxygen vacancies and??oxygen ions in the perovskite structural slabs, whereas the ion conductivity of Sr4Fe6O13+delta remains below 0.01 S cm.1 in the studied??conditions. The bonding energy of oxygen ions, evaluated from the formation enthalpy of n-type charge carriers, increases in the sequence??Sr4Fe6O13+delta < SrFeO3+delta < Sr3Fe2O6delta. These values correlate with thermodynamic stability of strontium ferrites at low p(O2). The??transition of SrFeO2.5+delta brownmillerite into disordered cubic phase above 850 .C leads to higher stability in reducing atmospheres. The??level of p-type conductivity is mainly governed by the concentration of electron holes, which was calculated from the oxygen content??determined by coulometric titration technique. The hole mobility, which is quite similar for all strontium ferrites and has a temperatureactivated??character, varies in the range 0.005.0.05 cm2 V.1 s.1 indicative of small-polaron conduction mechanism

\\\\Expert2\\nbo\\Solid State Sciences\\2004, v.6, N 9, p.907.pdf
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16.
Инвентарный номер: нет.
   
   H 99


   
    Ionic and electronic conductivity of La9.83-xPrxSi4.5Fe1.5O26 + or - delta apatites [] = Ionic and electronic conductivity of La9.83-xPrxSi4.5Fe1.5O26 + or - delta apatites / A. A. Yaremchenko, A. L. Shaula, V. V. Kharton, J. C. Waerenborgh, D. P. Rojas, M. V. Patrakeev, F. M. B. Marques // Solid State Ionics. - 2004. - V. 171, N 1-2. - С. 51-59. - Библиогр.: с. 59 (30 назв.) . - ISSN 0167-2738
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
АПАТИТЫ -- ИОННАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ ИОННАЯ -- ЧИСЛА ПЕРЕНОСА -- ЭЛЕКТРОННАЯ ПРОВОДИМОСТЬ -- ПРОВОДИМОСТЬ ЭЛЕКТРОННАЯ -- ИМПЕДАНС -- ТВЕРДЫЕ ЭЛЕКТРОЛИТЫ -- ЭЛЕКТРОЛИТЫ ТВЕРДЫЕ -- ОКСИДЫ -- МЕССБАУЭРОВСКАЯ СПЕКТРОСКОПИЯ -- СПЕКТРОСКОПИЯ МЕССБАУЭРОВСКАЯ
Аннотация: The incorporation of praseodymium in the apatite-type lattice of La9.83-xPrxSi4.5Fe1.5O26 + or - delta (x = 0-6) decreases the unit cell volume, suppresses Fe4+ formation according to Mossbauer spectroscopy, and increases p- and n-type electronic contributions to total conductivity, studied by the impedance spectroscopy and modified faradaic efficiency (FE) and electromotive force (EMF) methods at 973-1223 K. The additions of praseodymia have no essential effect on the ionic transport, with an activation energy of 99-109 kJ/mol, under oxidizing conditions. Contrary to the Al-containing analogue, La9.83Si4.5Al1.5O26, exhibiting p(O2)-independent conductivity at oxygen pressures from 10(-20) to 0.5 atm, the ionic conductivity of La9.83-xPrxSi4.5Fe1.5O26 + or - delta decreases on reducing p(O2) below 10(-14)-10(-12) atm. The observed behavior suggests a presence of hyperstoichiometric oxygen, critical for the level of ionic conduction and compensated by the formation of Fe4+ or
Pr4+. The ion transference numbers in air vary in the range 0.979-0.994 for La9.83-xPrxSi4.5Fe1.5O26+delta, whilst for La9.83Si4.5Al1.5O26 the p-type electronic contribution to the total conductivity is lower than 0.5%. The average thermal expansion coefficients (TECs) of silicate-based solid electrolytes are (8.8-9.4)x10(-6)K(-1) at 300-1200 K and (14.2-15.8)x10(-6)K(-1) at 1200-1350 K

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17.
Инвентарный номер: нет.
   
   V 86


    Volkov, V. L.
    Ionic Conductivity of (PbOH)2V12O31 · nH2O / V. L. Volkov, G. S. Zakharova // Inorganic Materials. - 2003. - Vol. 39, № 11. - P. 1188-1191 : il. - Bibliogr. : p. 1191 (5 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ИОННАЯ ПРОВОДИМОСТЬ -- ТЕРМООБРАБОТКА -- ПОЛИВАНАДАТЫ -- ЗОЛЬ-ГЕЛЬ МЕТОД
Аннотация: The 333-K complex impedance and temperature-dependent 10-kHz electrical conductivity of the cell Ni|(PbOH)2V12O31 · nH2O|Ni were measured. The results demonstrate that heat treatment changes the conductivity of (PbOH)2V12O31 · nH2O. After the removal of hydrate water, the activation energy for conduction in the range 203–485 K is 0.27 eV. The polarization resistance of the Ni electrodes is 31% of the total resistance of the cell at 296 K and is nearly zero above 303 K. The potential of the system lead polyvanadate/lead varies linearly with the Pb2+ concentration in aqueous Pb(NO3)2 solutions

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18.
Инвентарный номер: нет.
   
   L 27


   
    Lanthanum substituted CeNbO4+delta scheelites: mixed conductivity and structure at elevated temperatures [Текст] / R. J. Packer, S. J. Skinner, A. A. Yaremchenko, E. V. Tsipis, V. V. Kharton, M. V. Patrakeev, Yu. A. Bakhteeva // Journal of Materials Chemistry. - 2006. - Vol. 16, № 34. - С. 3503-3511. - Библиогр. : с. 3511 (17 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ЛАНТАН -- ПРОВОДИМОСТЬ -- СТЕХИОМЕТРИЯ -- ЦЕРИЙ
Аннотация: CeNbO4+d is a room temperature monoclinic material exhibiting a phase change to a tetragonal scheelite polymorph at 1023 K. The material can accommodate oxygen excess up to a composition of CeNbO4.25 in air which is believed to be incorporated on interstitial sites and hence is of interest for solid oxide fuel cell applications. Recent research however pointed to poor stability at low p(O2) making optimisation a necessity. To this end the effect of substituting lanthanum for cerium in CeNbO4+d has been investigated in terms of redox, structural and mixed conductive behaviour. On increasing lanthanum content the overall oxygen hyperstoichiometry of the as-prepared substituted phases was found to decrease. A reduction in the temperature of the monoclinic fergusonite to tetragonal scheelite phase transformation with increasing lanthanum content was also observed. However, the extent of oxidation with increasing temperature was found to decrease. Four probe dc conductivity measurements in the temperature range 923 K to 1223 K showed that the total conductivity decreased and that the p(O2) dependence of the total ionic conductivity increased with increasing lanthanum content. The ionic transference number, ti, was found to increase to a maximum of approximately 0.75 with lanthanum substitution but at low p(O2) the stability of the tetragonal phase was found to decrease

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19.
Инвентарный номер: нет.
   
   S 53


    Shaikhlislamova, A. R.
    Li+/H+ Ion Exchange in Li3 – 2xNbxM2 – x(PO4)3 (M = In, Fe) Materials with a NASICON Structure / A. R. Shaikhlislamova, N. A. Zhuravlev, A. B. Yaroslavtsev // Russian Journal of Inorganic Chemistry. - 2010. - Vol. 55, № 1. - P18-22 : il. - Bibliogr. : p. 22 (13 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ИОННЫЙ ОБМЕН -- ПРОТОННАЯ ПРОВОДИМОСТЬ
Аннотация: H3 – 2xNbxM2 – x(PO4)3 (M = In, Fe) acid phosphates have been obtained by ion exchange from their lithium forms and X ray powder diffraction, impedance measurements, and 7Li and 1H NMR spectroscopy. The parameters of the hexagonal unit cell of the proton exchanged forms differ only slightly from those of the initial lithium compounds. According to 1H NMR data, the proton in the acid phosphates is not hydrated. The conductivity of the acid phosphates at high temperatures depends weakly on their composition and is ~1.7 × 10–7 S cm–1 at 620 K. The activation energy of conduction is 30–33 kJ/mol (430–770 K)

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20.
Инвентарный номер: нет.
   
   L 81


   
    Lithium stoichiometry of solid electrolytes based on tetragonal Li7La3Zr2O12 / E. A. Il’ina, A. A. Raskovalov, P. Y. Shevelin, V. I. Voronin, I. F. Berger, N. A. Zhyravlev // Materials Research Bulletin. - 2014. - Vol. 53. - P32-37.
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
КЕРАМИКА -- ИМПЕДАНСНАЯ СПЕКТРОСКОПИЯ -- РАССЕЯНИЕ НЕЙТРОНОВ -- ИОННАЯ ПРОВОДИМОСТЬ
Аннотация: Samples of LixLa3Zr2O8.5+0.5x (x = 6, 7, 8, 9, 10) were synthesized with the citrate–nitrate method. Neutron diffraction studies have shown the presence of lithium carbonate impurities in the synthesized compounds. We propose a simple and effective method to determine the carbonate impurity content in the solid electrolytes. The technique is based on the measurement of the carbon dioxide volume produced from the interaction of the investigated material with acid. Determined in this way, the content of Li2CO3 in the synthesized electrolytes Li7La3Zr2O12, Li8La3Zr2O12.5 and Li9La3Zr2O13 are 1.32 ± 0.04, 1.95 ± 0.06 and 3.49 ± 0.10 wt.%, respectively. From the obtained data, the actual lithium content per formula unit of complex oxide was calculated for the synthesized compounds. The composition with x = 9 had the highest total conductivity, σ = 7.5 × 10−6 S cm−1, at room temperature. All the investigated electrolytes have an activation energy of approximately 50 kJ mol−1.

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