TY - JOUR
T1 - In Situ X-ray and Neutron Diffraction of the Rare-Earth Phosphate Proton Conductors Sr/Ca-Doped LaPO4 at Elevated Temperatures
AU - Al-Wahish, A.
AU - Al-Binni, U.
AU - Bridges, C. A.
AU - Tang, S.
AU - Bi, Z.
AU - Paranthaman, M. P.
AU - Huq, A.
AU - Mandrus, D.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/10/25
Y1 - 2016/10/25
N2 - We investigated the crystal structure, defect structure, and thermal stability of the rare-earth phosphate proton conductors (La,M)PO4 (where M = Sr, Ca) and obtained the thermal expansion coefficients, surface topography, size distribution, and proton conductivity. The study employed neutron powder diffraction (NPD) at elevated temperatures up to 800 °C, combined with powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and electrochemical impedance spectroscopy (EIS). Although the proton-oxygen site is located on the corners of the PO4 tetrahedra, the NPD shows an average bond length distortion in the hydrated 4.2% Sr/Ca-doped LaPO4. We investigated the proton dynamics by EIS and previously by Quasi-Elastic Neutron Scattering (QENS), and determined the bulk diffusion and the self-diffusion coefficients. Our results showed that QENS and EIS probe fundamentally different proton diffusion processes, where the EIS data reflect long-range intertetrahedral diffusion, whereas QENS probes more local diffusive motions.
AB - We investigated the crystal structure, defect structure, and thermal stability of the rare-earth phosphate proton conductors (La,M)PO4 (where M = Sr, Ca) and obtained the thermal expansion coefficients, surface topography, size distribution, and proton conductivity. The study employed neutron powder diffraction (NPD) at elevated temperatures up to 800 °C, combined with powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and electrochemical impedance spectroscopy (EIS). Although the proton-oxygen site is located on the corners of the PO4 tetrahedra, the NPD shows an average bond length distortion in the hydrated 4.2% Sr/Ca-doped LaPO4. We investigated the proton dynamics by EIS and previously by Quasi-Elastic Neutron Scattering (QENS), and determined the bulk diffusion and the self-diffusion coefficients. Our results showed that QENS and EIS probe fundamentally different proton diffusion processes, where the EIS data reflect long-range intertetrahedral diffusion, whereas QENS probes more local diffusive motions.
UR - http://www.scopus.com/inward/record.url?scp=84992743674&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.6b01531
DO - 10.1021/acs.chemmater.6b01531
M3 - Article
AN - SCOPUS:84992743674
SN - 0897-4756
VL - 28
SP - 7232
EP - 7240
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 20
ER -