TY - JOUR
T1 - Effect of Ca2+ Substitution on the Structure, Microstructure, and Microwave Dielectric Properties of Sr2Al2SiO7 Ceramic
AU - Manu, Kurusaroor Mana
AU - Karthik, Chinnathambi
AU - Ubic, Rick
AU - Sebastian, Mailadil Thomas
PY - 2013/12
Y1 - 2013/12
N2 - The effect of Ca2+ substitution on the structure, microstructure, and microwave dielectric properties of Sr-gehlenite (Sr 2Al2SiO7) ceramic has been investigated. The structure and microstructure of Sr2-xCaxAl 2SiO7 ceramics were analyzed via X-ray diffraction (XRD) as well as scanning and transmission electron microscopic techniques. While the end-members (x = 0 and 2) form isostructural compounds, a highly defective, nonstoichiometric, Ca-rich secondary phase was observed via bright-field transmission electron microscopy and energy dispersive X-ray spectroscopy in compositions corresponding to x = 0.75 and 1.5. The concentration of secondary phase in x = 0.75 is too low to be detected via XRD or scanning electron microscopy. Identical selected-area electron-diffraction patterns of the compounds (x = 0, 1, and 2) confirmed that they belong to the space group P4̄21m (no. 113) with tetragonal crystal symmetry. The porosity-corrected relative permittivity at microwave frequencies showed a gradual increase with Ca2+ content; however, Ca2+ substitution made only marginal changes to the microwave dielectric properties except in the case of x = 1.5, in which the secondary phase reduced the quality factor considerably. Thermal conductivity decreased with increasing Ca 2+ content, and the compounds with defective structures showed the lowest thermal conductivity. All the compounds exhibited low coefficients of linear thermal expansion, with values varying in the range 2.3-3.6 ppm/°C.
AB - The effect of Ca2+ substitution on the structure, microstructure, and microwave dielectric properties of Sr-gehlenite (Sr 2Al2SiO7) ceramic has been investigated. The structure and microstructure of Sr2-xCaxAl 2SiO7 ceramics were analyzed via X-ray diffraction (XRD) as well as scanning and transmission electron microscopic techniques. While the end-members (x = 0 and 2) form isostructural compounds, a highly defective, nonstoichiometric, Ca-rich secondary phase was observed via bright-field transmission electron microscopy and energy dispersive X-ray spectroscopy in compositions corresponding to x = 0.75 and 1.5. The concentration of secondary phase in x = 0.75 is too low to be detected via XRD or scanning electron microscopy. Identical selected-area electron-diffraction patterns of the compounds (x = 0, 1, and 2) confirmed that they belong to the space group P4̄21m (no. 113) with tetragonal crystal symmetry. The porosity-corrected relative permittivity at microwave frequencies showed a gradual increase with Ca2+ content; however, Ca2+ substitution made only marginal changes to the microwave dielectric properties except in the case of x = 1.5, in which the secondary phase reduced the quality factor considerably. Thermal conductivity decreased with increasing Ca 2+ content, and the compounds with defective structures showed the lowest thermal conductivity. All the compounds exhibited low coefficients of linear thermal expansion, with values varying in the range 2.3-3.6 ppm/°C.
UR - https://scholarworks.boisestate.edu/mse_facpubs/178
UR - https://doi.org/10.1111/jace.12598
U2 - 10.1111/jace.12598
DO - 10.1111/jace.12598
M3 - Article
SN - 0002-7820
VL - 96
SP - 3842
EP - 3848
JO - Journal of the American Ceramic Society
JF - Journal of the American Ceramic Society
IS - 12
ER -