Influence of the calcination procedure on the thermoelectric properties of calcium cobaltite Ca3Co4O9

被引:19
作者
Bresch, Sophie [1 ]
Mieller, Bjoern [1 ]
Selleng, Christian [2 ]
Stoecker, Thomas [3 ]
Moos, Ralf [3 ]
Rabe, Torsten [1 ]
机构
[1] Bundesanstalt Mat Forsch & Prufung BAM, Div Adv Tech Ceram, D-12203 Berlin, Germany
[2] Bundesanstalt Mat Forsch & Prufung BAM, Div Bldg Mat, D-12203 Berlin, Germany
[3] Univ Bayreuth, Dept Funct Mat, D-95447 Bayreuth, Germany
关键词
Thermoelectric oxides; Calcination; Solid-state-synthesis; Power factor; PHASE-EQUILIBRIA; TEMPERATURE; OXIDE; PERFORMANCE; CERAMICS; CA; MICROSTRUCTURE; ANISOTROPY; STATE; CR;
D O I
10.1007/s10832-018-0124-3
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Calcium cobaltite is one of the most promising oxide p-type thermoelectric materials. The solid-state reaction (or calcination, respectively), which is well known for large-scale powder synthesis of functional materials, can also be used for the synthesis of thermoelectric oxides. There are various calcination routines in literature for Ca3Co4O9 powder synthesis, but no systematic study has been done on the influence of calcination procedure on thermoelectric properties. Therefore, the influence of calcination conditions on the Seebeck coefficient and the electrical conductivity was studied by modifying calcination temperature, dwell time, particle size of raw materials and number of calcination cycles. This study shows that elevated temperatures, longer dwell times, or repeated calcinations during powder synthesis do not improve but deteriorate the thermoelectric properties of calcium cobaltite. Diffusion during calcination leads to idiomorphic grain growth, which lowers the driving force for sintering of the calcined powder. A lower driving force for sintering reduces the densification. The electrical conductivity increases linearly with densification. The calcination procedure barely influences the Seebeck coefficient. The calcination procedure has no influence on the phase formation of the sintered specimens.
引用
收藏
页码:225 / 234
页数:10
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