电解质
材料科学
氧化物
技术
高温电解
电极
热膨胀
电化学
化学工程
兴奋剂
热稳定性
电解
氧气
分析化学(期刊)
光电子学
复合材料
冶金
化学
天文
有机化学
色谱法
物理化学
工程类
物理
电离层
作者
Ziyi Zhu,Mingyang Zhou,Kai Tan,Zidai Fan,Dan Cao,Zhijun Liu,Meilong Chen,Yu Chen,Min Chen,Jiang Liu
标识
DOI:10.1021/acsami.3c00728
摘要
The solid oxide cell (SOC) based on a proton-conducting electrolyte is promising to play an important role in large-scale energy storage and hydrogen production. However, its development is hindered by performance degradation caused by the mismatch in thermal expansion coefficients (TECs) between the electrolyte and the oxygen electrode. Although there is work on reducing TECs of the oxygen electrode, it is difficult to find proper materials having a low TEC while maintaining a high performance. In this paper, we propose a new path to solve this problem: increasing the TEC of the electrolyte. We demonstrate that doping Fe into BaZr0.3Ce0.5Y0.1Yb0.1O3−δ (BZCYYb) can increase the TEC from 10.3 × 10–6 K–1 of BZCYYb to 13.4 × 10–6 K–1 of BaZr0.3Ce0.48Fe0.02Y0.1Yb0.1O3−δ (BZCYYbF). Fe doping also enhances the sinterability, electrochemical performance, and stability of the electrolyte. Meanwhile, we find that doping Fe into the oxygen electrode material PrNi0.5Co0.5O3−δ (PNC) decreases the TEC from 19.2 × 10–6 K–1 of PNC to 17.4 × 10–6 K–1 of PrNi0.4Co0.4Fe0.2O3−δ (PNCF). The improved stability of the SOC with the BZCYYbF electrolyte and the PNCF oxygen electrode is verified for steam electrolysis under a high steam partial pressure, 50%. Such a cell operates stably at a current density of 1.76 A cm–2 under 1.30 V and 700 °C for 150 h.
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