2020
DOI: 10.1016/j.jeurceramsoc.2019.10.005
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Impact of additives and processing on microstructure and dielectric properties of willemite ceramics for LTCC terahertz applications

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Cited by 41 publications
(26 citation statements)
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“…A higher willemite contribution caused an excessive increase in the sintering temperature. In previous studies [ 23 , 26 ], it was proved that both Zn 4 B 6 O 13 and Zn 2 SiO 4 ceramics do not react with silver, although the resolution, smoothness, and sharpness of the edges of the conductive patterns screen printed on the willemite-based substrates were better than those deposited on the zinc borate ceramics. Considering the requirements of a low sintering temperature suitable for cofiring with Ag-based commercial thick film pastes and the good quality of the printed conductors, the maximum preferred fraction of willemite in the Zn 4 B 6 O 13 - Zn 2 SiO 4 composites is limited to 60 wt %.…”
Section: Resultsmentioning
confidence: 99%
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“…A higher willemite contribution caused an excessive increase in the sintering temperature. In previous studies [ 23 , 26 ], it was proved that both Zn 4 B 6 O 13 and Zn 2 SiO 4 ceramics do not react with silver, although the resolution, smoothness, and sharpness of the edges of the conductive patterns screen printed on the willemite-based substrates were better than those deposited on the zinc borate ceramics. Considering the requirements of a low sintering temperature suitable for cofiring with Ag-based commercial thick film pastes and the good quality of the printed conductors, the maximum preferred fraction of willemite in the Zn 4 B 6 O 13 - Zn 2 SiO 4 composites is limited to 60 wt %.…”
Section: Resultsmentioning
confidence: 99%
“…For bulk ceramics, the fabrication procedure comprised solid-state synthesis of the components, milling of batches, uniaxial pressing of pellets, and sintering at 920–950 °C for 4 h. The starting components of the composites, Zn 4 B 6 O 13 and Zn 2 SiO 4 powders, were obtained via calcination at 900 °C and 1150 °C [ 23 , 26 ], respectively, followed by ball milling for 8 h (Pulverisette 5, Fritsch, Germany). The phase compositions of the powders after the synthesis and sintering processes were examined by the X-ray diffraction method, using Cu K α1 radiation within a 2Ɵ range of 5 to 90° (Empyrean, PANalytical, Almelo Netherlands The quantitative phase analysis and the crystal structure refinement were performed using the Rietveld method.…”
Section: Methodsmentioning
confidence: 99%
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