Comprehensive evaluation of dopant solubility, proton concentration, proton mobility and phase stability of lanthanum polyphosphate for conductivity improvement

被引:5
作者
Adachi, Yoshinobu [1 ]
Hatada, Naoyuki [1 ]
Uda, Tetsuya [1 ]
机构
[1] Kyoto Univ, Dept Mat Sci & Engn, Sakyo Ku, Yoshida Honmachi, Kyoto 6068501, Japan
关键词
Proton conductor; Fuel cells; PCFCs; DOPED BARIUM ZIRCONATE; WATER-VAPOR SOLUBILITY; MEMBRANES; LAPO4;
D O I
10.1016/j.ijhydene.2016.07.161
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lanthanum polyphosphate (LaP3O9) is a candidate for the electrolytes in protonic ceramic fuel cells (PCFCs). In this work, the solubility of dopants (Ca, Sr, Ba and Pb), proton concentration, and proton mobility in LaP3O9 were evaluated to clarify the limiting factors for conductivity improvement. The maximum doping levels of Ca, Sr, Ba, and Pb in LaP3O9 synthesized by precipitation method were about 8, 14, 3, and 6 mol% respectively. Here doping level is defined as the concentration ratio of the dopant (M) to the host cation (La) site ( M/(La + M)). The concentration ratio of protons to the dopant cations in doped LaP3O9, or hydration level, was almost independent of dopant species and as high as those in the perovskite-type oxides. The proton mobility in Sr-doped LaP3O9 was about twice those of Ca and Ba-doped LaP3O9, and it was similar to 7 times that of Pb-doped LaP3O9. Remarkably, the highest conductivity of Sr-doped LaP3O9 precipitated from phosphoric acid solution was about one order of magnitude higher than that synthesized by solid state reaction, and comparable to that of Sr(Zr0.9Y0.1)O3-delta. This conductivity enhancement should be attributed to the increase in Sr-doping level, reduction of grain boundary density and c-axis orientation of grains by the precipitation method. Nevertheless, instability of LaP3O9 in humidified hydrogen atmosphere should be a problem for the practical applications. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21450 / 21460
页数:11
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