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Sintering Behavior and Electrical Properties of Nanosized Doped‐ZnO Powders Produced by Metallorganic Polymeric Processing
Author(s) -
Durán Pedro,
Capel Francisco,
Tartaj Jesús,
Moure Carlos
Publication year - 2001
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.2001.tb00896.x
Subject(s) - materials science , sintering , ceramic , crystallite , doping , composite material , grain size , chemical engineering , calcination , shrinkage , microstructure , phase (matter) , mineralogy , metallurgy , optoelectronics , biochemistry , chemistry , organic chemistry , engineering , catalysis
Homogeneous and nanosized (28 nm crystallite size) doped‐ZnO ceramic powders were obtained by a metallorganic polymeric method. Calcining and granulating resulted in green compacts with uniform powder packing and a narrow pore‐size distribution (pore size 19 nm). Dense ceramic bodies (>99% of theoretical) were fabricated by normal liquid‐phase sintering at 850° and 940°C for 1–5 h. Apparently, the low pore‐coordination number allowed a uniform filling of the small pores by the liquid formed in the early stages of sintering, and, consequently, high shrinkage and rapid densification occurred in a short temperature interval (825°–850°C). At these sintering temperatures, limited grain growth occurred, and the grain size was maintained at <1 μm. Ceramics so‐fabricated showed a nonlinear coefficient, α, of ≥70, and a breakdown voltage, V b (1 mA/cm 2 ), of ≥1500 V/mm. The high electrical performance of the doped‐ZnO dense ceramics was attributed to liquid‐phase recession on cooling, which enhanced the ZnO‐ZnO direct contacts and the potential barrier effect.