氧化物
材料科学
电导率
氧化钇稳定氧化锆
电解质
离子电导率
电解
空位缺陷
化学工程
无机化学
立方氧化锆
化学
陶瓷
电极
冶金
物理化学
结晶学
工程类
作者
Andrew J. E. Rowberg,Heather S. Slomski,Namhoon Kim,Nicholas A. Strange,Brian P. Gorman,Sarah Shulda,David S. Ginley,Kyoung E. Kweon,Brandon C. Wood
标识
DOI:10.1021/acs.chemmater.4c00511
摘要
Solid-oxide electrolyzer cells (SOECs) based on a yttria-stabilized zirconia (YSZ) oxide electrolyte produce hydrogen from water with the assistance of excess thermal energy; however, Sr diffusion within the Gd-doped CeO<sub>2</sub> (GDC) barrier layer during processing or operation can lead to the formation of unwanted secondary phases such as SrO and SrZrO<sub>3</sub>. Here, to establish and compare the degree of impact of these phases on SOEC performance, we conduct first-principles calculations to study their bulk oxide conductivities and compare them to that of the YSZ electrolyte. We find that SrO has a low conductivity arising from the poor mobility and low concentration of mobile oxygen vacancies, and its presence in SOECs should therefore be avoided. SrZrO<sub>3</sub> also has a lower oxide conductivity than YSZ; however, this discrepancy is primarily due to lower vacancy concentrations rather than low mobility. We find that sufficient levels of Y-doping on the Zr site can increase oxygen vacancy concentrations in SrZrO<sub>3</sub> to achieve an oxide ionic conductivity on par with that of YSZ, thereby mitigating any potential deleterious effect on transport performance. Energy-dispersive X-ray spectroscopy confirms that Y is the most common minority element present in SrZrO<sub>3</sub> forming near the GDC–YSZ interface, alleviating concerns regarding the impact of SrZrO<sub>3</sub> on device performance. These results from our combined computational–experimental analysis can inform future engineering strategies designed to limit the detrimental effects of Sr-induced secondary phase formation on SOEC performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI