Journal
MATERIALS & DESIGN
Volume 132, Issue -, Pages 479-485Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2017.07.033
Keywords
ZnO; Electrical properties; Sintering; Microstructure
Categories
Funding
- National Basic Research Program of China [2013CB632900]
- National Natural Science Foundation of China [61137004, 61275181, 51202272]
- NSAF of China [U1330120]
- International AMP
- Technology Cooperation Program of China [2013DFG51570]
- Shanghai Municipal Science and Technology Commission [15DZ2260300]
- Training Scheme of Shanghai Yong Teachers
- Innovation Project of the Shanghai Institute of Ceramics
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Both the spark plasma sintering (SPS) method and reducing atmosphere sintering (N-2 + CO) method could greatly improve the electrical performance of ZnO-based thermoelectric materials. However, there is no comparison of these two methods which is essential for further improvements to the thermoelectric performance. In this article, a systematic comparison of the microstructures and electrical properties of the ZnO-based thermoelectric materials prepared by the SPS method, the reducing atmosphere sintering (N-2 + CO) method, and the conventional sintering method was presented. The ZnO-based thermoelectric materials prepared by the reducing atmosphere sintering (N-2 + CO) method showed the highest power factor with a moderate carrier concentration and a high Hall mobility, while the sample prepared by the SPS method exhibited the highest electrical conductivity of 2.3 x 105 S.m(-1) with a lower power factor. The ultra-high electrical conductivity of the SPS processed sample was mainly due to the increased solubility of Ti, which led to a higher carrier concentration. Moreover, the grain-boundary structure, which is important for the electrical performance, was also systematically analyzed by EBSD and CL. It can be concluded that the reducing atmosphere sintering (N-2 + CO) method is more suitable for thermoelectric applications, while the SPS method is an effective way to produce highly conductive ZnO ceramics. (C) 2017 Elsevier Ltd. All rights reserved.
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