溶解度
磷酸
无机化学
电导率
化学
离子电导率
离子
独居石
降水
相(物质)
二价
质子
离子键合
固溶体
结晶学
物理化学
地质学
锆石
古生物学
物理
有机化学
电极
量子力学
气象学
电解质
作者
Kenta K. Ohtaki,Neshat Jalali Heravi,Joanne W. Leadbetter,Peter E. D. Morgan,Martha L. Mecartney
标识
DOI:10.1016/j.ssi.2016.05.022
摘要
Monazite-type LnPO4 is a stable phase for many of the larger rare earths. The unusually asymmetric 9-fold coordinated La3 + sites can be substituted by other large ions including aliovalents such as Sr2 +. In the case of divalent ions, "charge balance" can be maintained by substituted monovalent anionic units such as (OH)−. The solid solution series has the chemical formula La1 − xSrxPO4 − x(OH)x, which may exist without defects such as vacancies as long as sufficient water is present. X up to as high as 0.3 is found, much higher than previously reported, when using a direct precipitation process in hot, strong phosphoric acid. Physical properties of Sr-doped LaPO4 up to that level, including proton transport, have been measured. At high temperatures, (> 400 °C) proton ionic conductivity in the bulk is expected to be high, but the structure becomes unstable. As (OH)− is given off, Sr also leaves the structure and forms an intergranular phase with phosphorus, a process that detrimentally affects the ionic conductivity and cannot be suppressed even when conducting measurements in water vapor that should encourage retaining (OH)− in the structure.
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