Phase formation and conductivity degradation of Sr1−xKxSiO3−0.5x ionic conductors. Issue 17 (4th April 2016)

• Record Type: Journal Article
• Authors: Xu, Jungu; Liu, Shuaibo; Wang, Quanchao; Xiaofeng, Junshu; Li, Xiaohui; Kuang, Xiaojun
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 17(2016)
• Page Start: 6313
• Page End: 6318
• Publication Date: 2016-04-04
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c6ta00666c
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Amorphous K2 Si2 O5 is responsible for the high ionic (not oxide ions) conductivity in Sr1− x K x SiO3−0.5 x materials. Abstract : The new ionic conductor Sr1− x K x SiO3−0.5 x was first reported by Singh et al. as a promising candidate electrolyte for solid oxide fuel cells. Here we report the thermal evolution of the phase formation and ionic conductivity of the composition x = 0.2. The results disclose the co-existence of crystalline and amorphous phases in the material at room temperature, and the amorphous phase would crystallize into K2 SiO3 and SiO2 on heating at ∼650 °C and return to the amorphous state at a temperature ≥1020 °C. Both the VT-XRD and conductivity data revealed that firing at a temperature above 1100 °C is favourable for maintaining the amorphous phase at ambient temperature. The phase evolution explains the conduction behavior. A K2 Si2 O5 glass was prepared in this work, and a high ionic conductivity was observed for this material, which was most likely responsible for the high ionic conductivity in Sr1− x K x SiO3−0.5 x ( x = 0.2). However, both the Sr1− x K x SiO3−0.5 x ( x = 0.2) and K2 Si2 O5 did not show strong evidence of oxide ion conduction.