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硅酸盐通报 ›› 2024, Vol. 43 ›› Issue (12): 4649-4656.

• 新型功能材料 • 上一篇    

A位缺陷型La6Sr0.3Cr0.5Fe0.5O3-δ材料的制备及电解CO2性能

常宏1,2, 牛佳春1   

  1. 1.太原工业学院材料工程系, 太原 030013;
    2.山西大学分子科学研究所, 山西省能源转换与存储重点实验室, 太原 030006
  • 收稿日期:2024-06-21 修订日期:2024-09-10 出版日期:2024-12-15 发布日期:2024-12-19
  • 作者简介:常 宏(1988—),男,博士,副教授。主要从事低浓度煤层气燃料电池发电研究及CO2电催化还原反应方面的研究。E-mail:changhong@tit.edu.cn
  • 基金资助:
    山西省基础研究计划青年项目(20210302124219);太原工业学院青年学术带头人支持计划资助(23020301)

Preparation and CO2 Electrolysis Performance of A-Site Deficient La6Sr0.3Cr0.5Fe0.5O3-δ Materials

CHANG Hong1,2, NIU Jiachun1   

  1. 1. Department of Materials Engineering, Taiyuan Institute of Technology, Taiyuan 030013, China;
    2. Key Lab Mat Energy Convers & Storage, Institute of Molecular Science, Shanxi University, Taiyuan 030006, China
  • Received:2024-06-21 Revised:2024-09-10 Published:2024-12-15 Online:2024-12-19

摘要: 为了进一步提高La0.7Sr0.3Cr0.5Fe0.5O3-δ(LSCrF)基钙钛矿型氧化物的催化活性,在LSCrF材料的A位引入非化学计量缺陷,制备了A位缺陷型La0.6Sr0.3Cr0.5Fe0.5O3-δ(A-LSCrF),并通过X射线衍射(XRD)、扫描电子显微镜(SEM)、比表面及孔隙度分析(BET)、热重分析(TGA)以及电化学测试等综合表征技术,探究了材料的物理化学性质及电化学性能。结果表明,A-LSCrF样品粉体颗粒均匀,比表面积和平均孔径分别为1.70 m2·g-1和14.08 nm,且在工作条件下会产生更多氧空穴,这有利于提高A-LSCrF的催化活性。在2.00 V时LSCrF基单电池的电流密度为0.73 A·cm-2,而A-LSCrF基单电池的电流密度可达1.38 A·cm-2。以上结果说明A位引入非化学计量缺陷可以有效增加A-LSCrF氧空穴的浓度,从而提高A-LSCrF电解CO2的性能。

关键词: 固体氧化物电解池, 燃料极, A位缺陷, 氧空穴, 催化活性, 电化学性能

Abstract: To further enhance the catalytic activity of the perovskite-type oxide La0.7Sr0.3Cr0.5Fe0.5O3-δ(LSCrF), non-stoichiometric defects were introduced at the A-site of the LSCrF material to prepare A-site deficient La0.6Sr0.3Cr0.5Fe0.5O3-δ(A-LSCrF). The physical-chemical properties and electrochemical performance of the materials were investigated using a comprehensive set of characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) analysis, thermogravimetric analysis (TGA), and electrochemical testing. The results indicate that the A-LSCrF sample exhibits uniform particle sizes, with a specific surface area and mean pore diameter of 1.70 m2·g-1 and 14.08 nm, respectively. Under operating conditions, it generates a higher concentration of oxygen vacancies, which is beneficial in boosting catalytic activity. At 2.00 V, the current density of the LSCrF-based single cell is 0.73 A·cm-1, whereas the A-LSCrF-based single cell achieves a current density of 1.38 A·cm-1. These findings suggest that the introduction of A-site defects effectively increases the concentration of oxygen vacancies, thereby enhancing the cell’s performance in electrochemical CO2 reduction.

Key words: solid oxide electrolytic cell, fuel electrode, A-site deficient, oxygen vacancy, catalytic activity, electrochemical performance

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