Entropy of oxidation and redox energetics of CaMnO3-δ

被引:39
作者
Bakken, E
Boerio-Goates, J
Grande, T
Hovde, B
Norby, T
Rormark, L
Stevens, R
Stolen, S
机构
[1] Univ Oslo, Dept Chem, N-0315 Oslo, Norway
[2] Univ Oslo, Ctr Mat Sci & Nanotechnol, N-0315 Oslo, Norway
[3] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
[4] Norwegian Univ Sci & Technol, Dept Mat Technol, N-7491 Trondheim, Norway
关键词
CaMnO3-delta; non-stoichiometry; redox; entropy of oxidation; polyhedron preference;
D O I
10.1016/j.ssi.2005.06.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The heat capacities of CaMnO3 and CaMnO2.562 from 10 to 600 K are determined by adiabatic calorimetry and used to derive an average entropy for the following oxidation reaction 4CaMnO(2.50) + O-2(g) = 4CaMnO(3) The redox energetics of CaMnO3-delta is analysed using four independent sets of experimental data: the entropy of oxidation reported here, the enthalpy of oxidation previously determined by reaction calorimetry and by coloumetric titration as well as data for the oxygen-stoichiometry of CaMnO3-delta as function of partial pressure of oxygen and temperature. We show very clearly the importance of experimental data for the non-configurational entropy. A solution model, in which a random distribution of oxygen atoms and oxygen vacancies on the O-sub-lattice is the main contribution to the structural disorder, largely reproduces the experimental data. The analysis furthermore suggests an energetic preference for square pyramidal coordination for manganese in CaMnO3-delta. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:2261 / 2267
页数:7
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