无机材料学报 ›› 2026, Vol. 41 ›› Issue (7): 965-973.DOI: 10.15541/jim20250496

• 研究论文 • 上一篇    下一篇

表面修饰LSCF-GDC多相复合空气电极的高效构筑与性能优化

沈雪松1(), 谢凯峰2,3, 薛强3, 郑国柱3, 肖国萍2, 陈婷3(), 陈文淼1(), 王绍荣3   

  1. 1 山东国创燃料电池技术创新中心有限公司, 潍坊 261061
    2 中国科学院 上海应用物理研究所, 上海 201800
    3 中国矿业大学 化工学院, 徐州 221116
  • 收稿日期:2025-12-14 修回日期:2026-02-26 出版日期:2026-04-03 网络出版日期:2026-04-03
  • 通讯作者: 陈 婷, 副教授. E-mail: chenting@cumt.edu.cn;
    陈文淼, 教授级高级工程师. E-mail: chenwm@weichai.com
  • 作者简介:沈雪松(1990-), 男, 博士. E-mail: shenxuesong@nctifc.com
  • 基金资助:
    国家燃料电池技术创新中心开放基金(nctifc-sq-2024-138);国家重点研发项目(2024YFF0506300);国家自然科学基金(52572283);泰山产业领军人才工程(tscx202312126);中国博士后基金(2023M743769)

High-efficiency Construction and Performance Optimization of Surface-modified LSCF-GDC Multiphase Composite Air Electrodes

SHEN Xuesong1(), XIE Kaifeng2,3, XUE Qiang3, ZHENG Guozhu3, XIAO Guoping2, CHEN Ting3(), CHEN Wenmiao1(), WANG Shaorong3   

  1. 1 Shandong Guochuang Fuel Cell Technology Innovation Center Co., Ltd., Weifang 261061, China
    2 Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China
    3 School of Chemical Engineering & Technology, China University of Mining and Technology, Xuzhou 221116, China
  • Received:2025-12-14 Revised:2026-02-26 Published:2026-04-03 Online:2026-04-03
  • Contact: CHEN Ting, associate professor. E-mail: chenting@cumt.edu.cn;
    CHEN Wenmiao, professor. E-mail: chenwm@weichai.com
  • About author:SHEN Xuesong (1990-), male, PhD. E-mail: shenxuesong@nctifc.com
  • Supported by:
    Open Fund of the National Fuel Cell Technology Innovation Center(nctifc-sq-2024-138);National Key R&D Program of China(2024YFF0506300);National Natural Science Foundation of China(52572283);Taishan Industrial Experts Program(tscx202312126);China Postdoctoral Science Foundation(2023M743769)

摘要:

为实现可逆固体氧化物电池(RSOCs)在中低温下的高效运行, 开发高性能空气电极至关重要。本研究针对传统La0.6Sr0.4Co0.2Fe0.8O3-δ-Gd0.2Ce0.8O3-δ (LSCF-GDC)空气电极在中低温下氧还原反应(ORR)和氧析出反应(OER)活性不足的问题, 采用简单经济的浸渍法, 在LSCF-GDC空气电极骨架上构建纳米催化剂。通过系统优化空气电极烧结温度、催化剂种类及负载量, 确定Pr0.5Sr0.5CoO3-δ (PSC)为最优的改性催化剂。改性后对称电池在600 ℃下的极化阻抗(Rp)为0.16 Ω·cm2, 较空白LSCF-GDC空气电极降低了71.4% (0.56 Ω·cm2)。这是因为PSC纳米颗粒协同优化了氧扩散、表面交换与离子传导过程, 显著提升了ORR/OER动力学。在单电池测试中, 700 ℃、燃料电池(FC)模式下的峰值功率密度为1.23 W·cm-2, 较空白LSCF-GDC电池性能提升92.19%; FC与电解池(EC)模式下稳定性均显著增强。PSC表面修饰是全面提升LSCF-GDC空气电极综合性能的有效策略, 对推进中低温RSOCs技术发展具有重要意义。

关键词: 可逆固体氧化物电池, 空气电极, 表面修饰, Pr0.5Sr0.5CoO3-δ催化剂, 氧还原/析出反应

Abstract:

To enable the efficient operation of reversible solid oxide cells (RSOCs) at intermediate or lower temperatures, the development of high-performance air electrodes is crucial. This work addresses the insufficient oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity of the conventional La0.6Sr0.4Co0.2Fe0.8O3-δ-Gd0.2Ce0.8O3-δ (LSCF-GDC) air electrode at these temperatures by constructing a nanocatalyst coating on the LSCF-GDC electrode skeleton via a simple and cost-effective infiltration method. Through systematic optimization of the sintering temperature, loading amount and type of catalysts, Pr0.5Sr0.5CoO3-δ (PSC) is confirmed as the optimal catalyst for modification. The modified symmetrical cell exhibits a polarization resistance (Rp) of 0.16 Ω·cm2 at 600 ℃, 71.4% lower than that of the pristine LSCF-GDC air electrode (0.56 Ω·cm2). Relaxation time distribution analysis indicates that PSC nanoparticles significantly enhance the ORR/OER kinetics by synergistically optimizing oxygen diffusion, surface exchange, and ion transport processes. The single cell with PSC modification achieves an outstanding peak power density of 1.23 W·cm-2 in the fuel cell (FC) mode at 700 ℃ with a 92.19% enhancement. Both FC and electrolysis cell (EC) modes modified with nano-PSC exhibit superior long-term stabilities. This study demonstrates that PSC impregnation modification is an effective strategy for comprehensively improving the overall performance of LSCF-GDC air electrodes, which is of great significance for promoting intermediate temperature RSOC technology.

Key words: reversible solid oxide cell, air electrode, surface modification, Pr0.5Sr0.5CoO3 catalyst, oxygen reduction/ evolution reaction

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