Milad Moazzam , Giulio Cordaro , Maxime Vallet , Vincent Boemare , Nicolas Guiblin , Guilhem Dezanneau
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Analytical techniques such as X-ray diffraction (XRD) at room and high temperatures, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), dilatometry (TEC), and 4-probe conductivity measurements were employed to characterize exhaustively structural, thermal and electrical properties of the samples. The electrochemical characterization was further investigated through electrochemical impedance spectroscopy (EIS) as well as fuel cell testing conducted on electrolyte-supported symmetrical cells. XRD showed that all samples have a cubic structure with the <span><math><mi>Pm</mi><mover><mn>3</mn><mo>¯</mo></mover><mi>m</mi></math></span> space group. However, during TEM experiments, it was observed that SmBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> presents a quintuple nano-ordering perovskite structure. Pr-based sample shows the highest electrical conductivity (68 S cm<sup>−1</sup> at 500 °C), while NdBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> presents the lowest area specific resistance in air (0.47 Ω cm<sup>2</sup> at 600 °C) revealing that the disordered perovskite structure is more efficient than the quintuple nano-ordered phase of SmBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> in the oxygen reduction reaction (ORR). The use of NdBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> as electrodes in symmetrical cells has been demonstrated between 500 °C and 600 °C.</p></div>","PeriodicalId":431,"journal":{"name":"Solid State Ionics","volume":"417 ","pages":"Article 116689"},"PeriodicalIF":3.0000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Study of REBa2Fe3O8+δ (RE = Pr, Nd, Sm) layered perovskites as cobalt-free electrodes for symmetrical solid oxide fuel cells\",\"authors\":\"Milad Moazzam , Giulio Cordaro , Maxime Vallet , Vincent Boemare , Nicolas Guiblin , Guilhem Dezanneau\",\"doi\":\"10.1016/j.ssi.2024.116689\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The <em>RE</em>Ba<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> (<em>RE</em> = Nd, Sm, Pr) perovskites are investigated as potential cobalt-free electrodes in symmetrical solid oxide fuel cells (SOFCs). After the preparation of samples by a soft chemistry route, we first characterized the intrinsic properties and then determined the electrochemical performance after the deposition of porous electrodes to obtain symmetrical cells. Analytical techniques such as X-ray diffraction (XRD) at room and high temperatures, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), dilatometry (TEC), and 4-probe conductivity measurements were employed to characterize exhaustively structural, thermal and electrical properties of the samples. The electrochemical characterization was further investigated through electrochemical impedance spectroscopy (EIS) as well as fuel cell testing conducted on electrolyte-supported symmetrical cells. XRD showed that all samples have a cubic structure with the <span><math><mi>Pm</mi><mover><mn>3</mn><mo>¯</mo></mover><mi>m</mi></math></span> space group. However, during TEM experiments, it was observed that SmBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> presents a quintuple nano-ordering perovskite structure. Pr-based sample shows the highest electrical conductivity (68 S cm<sup>−1</sup> at 500 °C), while NdBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> presents the lowest area specific resistance in air (0.47 Ω cm<sup>2</sup> at 600 °C) revealing that the disordered perovskite structure is more efficient than the quintuple nano-ordered phase of SmBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> in the oxygen reduction reaction (ORR). The use of NdBa<sub>2</sub>Fe<sub>3</sub>O<sub>8+δ</sub> as electrodes in symmetrical cells has been demonstrated between 500 °C and 600 °C.</p></div>\",\"PeriodicalId\":431,\"journal\":{\"name\":\"Solid State Ionics\",\"volume\":\"417 \",\"pages\":\"Article 116689\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Solid State Ionics\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0167273824002376\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solid State Ionics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167273824002376","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
我们将 REBa2Fe3O8+δ(RE = Nd、Sm、Pr)包晶石作为对称固体氧化物燃料电池(SOFC)中潜在的无钴电极进行了研究。通过软化学方法制备样品后,我们首先确定了样品的内在特性,然后测定了多孔电极沉积后的电化学性能,从而获得了对称电池。我们采用了室温和高温 X 射线衍射 (XRD)、透射电子显微镜 (TEM)、热重分析 (TGA)、扩张仪 (TEC) 和四探针电导率测量等分析技术,对样品的结构、热和电特性进行了详尽的表征。通过电化学阻抗谱(EIS)以及在电解质支持的对称电池上进行的燃料电池测试,进一步研究了电化学特性。XRD 显示,所有样品都具有 Pm3¯m 空间群的立方结构。然而,在 TEM 实验中观察到,SmBa2Fe3O8+δ 呈现出五重纳米排序的包晶结构。基于 Pr 的样品显示出最高的导电性(500 ℃ 时为 68 S cm-1),而 NdBa2Fe3O8+δ 在空气中显示出最低的面积比电阻(600 ℃ 时为 0.47 Ω cm2),这表明在氧还原反应(ORR)中,无序的包晶结构比 SmBa2Fe3O8+δ 的五重纳米有序相更有效。在 500 °C 至 600 °C 的对称电池中使用 NdBa2Fe3O8+δ 作为电极已得到证实。
Study of REBa2Fe3O8+δ (RE = Pr, Nd, Sm) layered perovskites as cobalt-free electrodes for symmetrical solid oxide fuel cells
The REBa2Fe3O8+δ (RE = Nd, Sm, Pr) perovskites are investigated as potential cobalt-free electrodes in symmetrical solid oxide fuel cells (SOFCs). After the preparation of samples by a soft chemistry route, we first characterized the intrinsic properties and then determined the electrochemical performance after the deposition of porous electrodes to obtain symmetrical cells. Analytical techniques such as X-ray diffraction (XRD) at room and high temperatures, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), dilatometry (TEC), and 4-probe conductivity measurements were employed to characterize exhaustively structural, thermal and electrical properties of the samples. The electrochemical characterization was further investigated through electrochemical impedance spectroscopy (EIS) as well as fuel cell testing conducted on electrolyte-supported symmetrical cells. XRD showed that all samples have a cubic structure with the space group. However, during TEM experiments, it was observed that SmBa2Fe3O8+δ presents a quintuple nano-ordering perovskite structure. Pr-based sample shows the highest electrical conductivity (68 S cm−1 at 500 °C), while NdBa2Fe3O8+δ presents the lowest area specific resistance in air (0.47 Ω cm2 at 600 °C) revealing that the disordered perovskite structure is more efficient than the quintuple nano-ordered phase of SmBa2Fe3O8+δ in the oxygen reduction reaction (ORR). The use of NdBa2Fe3O8+δ as electrodes in symmetrical cells has been demonstrated between 500 °C and 600 °C.
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