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Heat capacity and other thermodynamic properties of CoTe2 from 5 to 1 030 K and of CoTe2.315 from 300 to 1 040 K
Authors:Jose A. R. Cheda  Edgar F. Westrum Jr.  Fredrik Grønvold
Affiliation:(1) Department of Chemistry, University of Michigan, 48109 Ann Arbor, MI, USA;(2) Department of Chemistry, University of Oslo, Blindern, 0315 Oslo 3, Norway;(3) Present address: Departamento de Quimica Fisica, Facultad de Quimicas, Universidad Complutense, Madrid 3, Spain
Abstract:The heat capacity of orthorhombic (marcasite-type structure) cobalt ditelluride has been measured from 5 to 1 030 K by adiabatic-shield calorimetry with alternate energy inputs and equilibrations. Above 900 K a marked increase in heat capacity occurs which probably signals a change in the composition of the CoTe2-phase towards higher tellurium content. Values at 298.15 and 1 000 K in J K–1 mol–1 of the heat capacity (Cp,m), entropy [Sm°(T)Sm°(0)], andGibbs energy function – [Gm°(T)Hm°(0)]T–1 are 75.23, 114.5, 49.93, and 132.4, 216.2, 139.17, respectively. Consistent with the metallic behavior of CoTe2, deviation of the heat capacity from theDebye T3-law was found at low temperatures. Comparison with the heat capacity of FeTe2 shows aSchottky-like deviation with a maximum of 7.3 J K–1 mol–1 at 80 K and evidences the influence of the additional 3 d-electron in cobalt compared to iron. Heat capacity measurements were made on CoTe2.33 to ascertain the existence range of the CoTe2+x-phase and the entropy of the associated structural disorder.The portion of this research done at Ann Arbor was supported in part by the Structural Chemistry and Chemical Thermodynamics Program of the Division of Chemistry of the National Science Foundation under Grant No. CHE-7710049.
Keywords:Cobalt telluride  Cobalt ditelluride  Heat capacity  3d Electrons  Schottky contributions  Thermophysics
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