Enhancement of sintering rates in BaTiO3 by controlling of DC electric current
Source abstract
Abstract
DC electric fields ranged from 25 to 350 V/cm enhanced the sintering rates of BaTiO3. At the field of 25 V/cm, the sintering densification occurred by field-assisted sintering (FAST), and flash-sintering preceded by FAST was observed at the field strength of more than 75 V/cm. Most of the densification, however, was produced by the FAST process. At high field strength of more than 250 V/cm, the sintering densification was not finished owing to discharging during the flash-sintering. By means of FAST process at 100 V/cm and the current limit of 100 mA, in contrast, relative density of 97% and a fine grain size about 500 nm were achieved at 1020°C in the present material. The FAST process, where the electric current was set to the transition current between FAST and flash-sintering, is highly effective to fabricate uniform and fine grained BaTiO3 polycrystal.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ferroelectric and Piezoelectric Materials · Electronic and Structural Properties of Oxides · Advanced ceramic materials synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nagoya University, Department of Quantum Engineering
National Institute for Materials Science
References (13)
Show source-provided references
1. 1) D. Yang, R. Raj and H. Conrad, J. Am. Ceram. Soc., 93, 2935–2937 (2010).10.1111/j.1551-2916.2010.03905.x ↗
2. 2) D. Yang and H. Conrad, Scr. Mater., 63, 328–331 (2010).10.1016/j.scriptamat.2010.04.030 ↗
3. 3) M. Cologna, B. Rashkova and R. Raj, J. Am. Ceram. Soc., 93, 3556–3559 (2010).10.1111/j.1551-2916.2010.04089.x ↗
4. 4) M. Cologna, L. G. A. Prette and R. Raj, J. Am. Ceram. Soc., 94, 316–319 (2011).10.1111/j.1551-2916.2010.04267.x ↗
5. 5) J. S. C. Francis, M. Cologna, D. Montinaro and R. Raj, J. Am. Ceram. Soc., 96, 1342–1344 (2013).10.1111/jace.12281 ↗
6. 6) A. L. G. Prette, M. Cologna, V. Sglavo and R. Raj, J. Power Sources, 196, 2061–2065 (2011).10.1016/j.jpowsour.2010.10.036 ↗
7. 7) M. Cologna, J. S. C. Francis and R. Raj, J. Eur. Ceram. Soc., 31, 2827–2837 (2011).10.1016/j.jeurceramsoc.2011.07.004 ↗
8. 8) A. Karakuscu, M. Cologna, D. Yarotski, J. Won, J. S. C. Francis and R. Raj, J. Am. Ceram. Soc., 95, 2531–2536 (2012).10.1111/j.1551-2916.2012.05240.x ↗
9. 9) H. Yoshida, Y. Sakka, T. Yamamoto, J. M. Lebrunc and R. Raj, J. Eur. Ceram. Soc., 34, 991–1000 (2014).10.1016/j.jeurceramsoc.2013.10.031 ↗
10. 10) K. J. Shikhar and R. Raj, J. Am. Ceram. Soc., 97, 527–534 (2014).10.1111/jace.12682 ↗
11. 11) J. C. M’Peko, J. S. C. Francis and R. Raj, J. Eur. Ceram. Soc., 34, 3655–3600 (2014).10.1016/j.jeurceramsoc.2014.04.041 ↗
12. 12) D. K. Lee, H. I. Yoo and K. D. Becher, Solid State Ionics, 154–155, 189–193 (2002).10.1016/S0167-2738(02)00427-7 ↗
13. 13) N. H. Chan, R. K. Sharma and D. M. Smyth, J. Am. Ceram. Soc., 64, 556–562 (1981).10.1111/j.1151-2916.1981.tb10325.x ↗