Sintering composite electrolytes of yttria-doped bismuth oxide and yttria-stabilized zirconia for solid oxide fuel cells

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY Journal of Solid State Electrochemistry Pub Date : 2024-08-02 DOI:10.1007/s10008-024-06030-1
Yuling Xia, Lijie Zhang, Kang Zhu, Binze Zhang, Changrong Xia
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Abstract

Solid oxide fuel cell (SOFC) with high conversion efficiency has drawn great attention for a sustainable future. Its electrolyte, typically yttria-stabilized zirconia (YSZ), is usually sintered above 1400 °C with commercially available powder materials. To lower the sintering temperature, yttria-doped bismuth oxide (YDB) is investigated in this work as an additive to form composite electrolytes. Dilatometric analysis reveals that the temperature corresponding to the maximum shrinkage rate is decreased from 1260 to 870 °C by YDB. Meanwhile, adding YDB results in the formation of poor conductive second phase monoclinic zirconia (m-ZrO2), especially when YDB content reaches 3 mol%. Thus, total conductivity decreases and then increases with YDB content. It is noted that the grain boundary conductivity is substantially improved, which is caused by bismuth enrichment at the grain boundary region of the dense composite electrolyte.

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用于固体氧化物燃料电池的掺钇氧化铋和钇稳定氧化锆烧结复合电解质
具有高转换效率的固体氧化物燃料电池(SOFC)在可持续发展的未来备受关注。其电解质通常为钇稳定氧化锆(YSZ),通常使用市售粉末材料在 1400 °C 以上烧结。为了降低烧结温度,本研究将掺钇氧化铋(YDB)作为添加剂,以形成复合电解质。稀释分析表明,YDB 可将最大收缩率对应的温度从 1260 ℃ 降至 870 ℃。同时,添加 YDB 会形成导电性较差的第二相单斜氧化锆(m-ZrO2),尤其是当 YDB 含量达到 3 摩尔%时。因此,随着 YDB 含量的增加,总电导率先降低后升高。值得注意的是,晶界电导率得到了大幅提高,这是由于铋在致密复合电解质的晶界区域富集所致。
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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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