材料科学
电极
电解
氧化物
氢
流延
克拉克电极
化学工程
高温电解
相位反转
固体氧化物燃料电池
制氢
氢燃料
阳极
功率密度
电解槽
纳米技术
烧结
电解质
燃料电池
复合材料
冶金
化学
膜
功率(物理)
生物化学
量子力学
物理化学
工程类
有机化学
物理
作者
Meiting Yang,Chang‐Jiang Yang,Mingzhuang Liang,Guangming Yang,Ran Ran,Wei Zhou,Zongping Shao
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-12-01
卷期号:27 (23): 8396-8396
被引量:13
标识
DOI:10.3390/molecules27238396
摘要
Solid oxide cells (SOCs) have been considered as a promising energy conversion and storage device. However, state-of-the-art cells’ practical application with conventionally fabricated Ni-(Y2O3)0.08(ZrO2)0.92 (YSZ) cermet hydrogen electrode and La0.8Sr0.2MnO3 perovskite oxygen electrode is strongly limited by the unsatisfactory performance. Instead, new advances in cell materials and fabrication techniques that can lead to significant performance enhancements are urgently demanded. Here, we report a high-performance reversible SOC that consisted of a combination of SrSc0.175Nb0.025Co0.8O3−δ (SSNC) and phase-inversion tape-casted Ni-YSZ, which served as the oxygen and hydrogen electrode, respectively. The hydrogen electrode synthesized from phase-inversion tape-casting showed a high porosity of 60.8%, providing sufficient active sites for hydrogen oxidation in the solid oxide fuel cell (SOFC) mode and H2O electrolysis in the solid oxide electrolysis cell (SOEC) mode. Accordingly, it was observed that the maximum power density of 2.3 W cm−2 was attained at 750 °C in SOFC mode and a current density of −1.59 A cm−2 was obtained at 1.3 V in SOEC mode. Hence, these results reveal that the simultaneous optimization of oxygen and hydrogen electrodes is a pragmatic strategy that improves the performance of SOCs, which may significantly accelerate the commercialization of such an attractive technology.
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