Microstructure, conductivity and mechanical properties of calcia stabilized zirconia ceramics obtained from nanosized precursor and reduced graphene oxide doped precursor powders

被引:19
作者
Kurapova, Olga Yu [1 ,2 ]
Glumov, Oleg, V [1 ]
Lomakin, Ivan, V [1 ]
Golubev, Sergey N. [2 ]
Pivovarov, Mikhail M. [2 ]
Krivolapova, Julia, V [1 ]
Konakov, Vladimir G. [1 ,2 ,3 ]
机构
[1] St Petersburg State Univ, Univ Skya Nab 7-9, St Petersburg 199034, Russia
[2] Glass & Ceram Ltd, 9th Line VO 20 Lit A,Off 2H, St Petersburg 199004, Russia
[3] Inst Problems Mech Engn VO, Bolshoj Pr 61, St Petersburg 199178, Russia
基金
俄罗斯科学基金会;
关键词
ZrO2; Ionic conductivity; Grain boundaries; Impedance spectroscopy; Hardness; Reduced graphene oxide; EFFUSION MASS-SPECTROMETRY; THERMODYNAMIC PROPERTIES; ELECTROLYTES; IMPEDANCE; COMPOSITES; SCANDIA; SYSTEM; BULK;
D O I
10.1016/j.ceramint.2018.05.202
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
In the work 12CaO-88ZrO(2) (12CSZ, mol%) ceramics was manufactured both from nanopowder, obtained via cryochemical technique, and composite precursor 12CSZ + 0.25 wt% rGO (reduced graphene oxide). Via SEM, XRD and Raman spectroscopy the detailed investigation of the effect of the precursor type and intermediate processing on the microstructure and electrical conductivity of ceramics was carried out. It was shown that rGO is completely removed during the annealing at 1550 degrees C for 3 h in air with no effect on the high ionic conductivity of ceramics. The use of nanosized powder and the additional processing step results in vacuum dense solid electrolytes characterized by well-formed cubic zirconia based solid solution, thin discontinuous grain boundaries and rather high ionic conductivity. The addition of rGO leads to slight microhardness (HV) decrease comparing to ceramics manufactured from the nanosized precursor. As a result, a new technique for zirconia based solid electrolytes having both high electrical conductivity at high temperatures and sufficient mechanical properties was suggested.
引用
收藏
页码:15464 / 15471
页数:8
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