Co-doped willemite ceramic pigments: Technological behaviour, crystal structure and optical properties

被引:70
作者
Ozel, Emel [2 ]
Yurdakul, Hilmi [2 ]
Turan, Servet [2 ]
Ardit, Matteo [1 ]
Cruciani, Giuseppe [1 ]
Dondi, Michele [3 ]
机构
[1] Univ Ferrara, Dept Earth Sci, I-44100 Ferrara, Italy
[2] Anadolu Univ, Dept Mat Sci & Engn, TR-26480 Eskisehir, Turkey
[3] CNR, ISTEC, I-48018 Faenza, Italy
关键词
Electron microscopy; Spectroscopy; X-ray methods; Optical properties; Willemite; ELECTRON-MICROSCOPE; GLASS-CERAMICS; THIN-FILMS; PHOSPHORS; LUMINESCENCE; ZN2SIO4-MN; EELS;
D O I
10.1016/j.jeurceramsoc.2010.08.013
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
Cobalt-doped willemite is a promising blue ceramic pigment, but some important aspects concerning crystal structure, optical properties and technological behaviour are still undisclosed. In order to get new insight on these features, willemite pigments (Zn2-xCoxSiO4, 0 <x <0.3) were synthesized by the ceramic route and characterized from the structural (XRPD with Rietveld refinement), optical (DRS and colorimetry), microstructural (SEM, STEM, TEM, EDX, EELS) and technological (simulation of the ceramic process) viewpoints. The incorporation of cobalt in the willemite lattice, taking preferentially place in the Zn1 tetrahedral site, induces an increase of unit-cell parameters, metal-oxygen distances, and inter-tetrahedral tilting. It causes shifting and enhanced splitting of spin-allowed bands of Co2+ in tetrahedral coordination, implying slight changes of crystal field strength Dq and Racah B parameter, but increasing spin-orbit coupling parameter lambda. Willemite pigments impart deep blue hue to ceramic glazes and glassy coatings with a colouring performance better than commercial Co-bearing colorants in the 800-1200 degrees C range. Detailed SEM-TEM investigation and microanalysis proved that no diffusion phenomena occur at the pigment-glassy coating interface and that willemite pigments are chemically inert during firing at 1050 degrees C. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3319 / 3329
页数:11
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