A novel Co-free and efficient Pr0.5Ba0.5Fe0.8Cu0.2O3-δ nanofiber cathode material for intermediate temperature solid oxide fuel cells

IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Ceramics International Pub Date : 2024-09-28 DOI:10.1016/j.ceramint.2024.09.369
Youjie Zhang , Jie Yang , Defeng Zhou , Xiaofei Zhu , Ning Wang , Jinghe Bai , Yaping Zhang , Yuqian Wang , Wenfu Yan
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Abstract

Fe-based perovskite without Co has a low thermal expansion coefficient and can be used as a solid oxide fuel cell (SOFC) cathode to ensure the thermal compatibility with the electrolyte; however, its further advancement is impeded by sluggish oxygen reduction reaction (ORR) dynamics. In this work, the electrospinning method and Cu doping strategy are employed to improve the microstructure and oxygen reduction kinetics of Pr0.5Ba0.5FeO3-δ cathodes. The results show that Pr0.5Ba0.5Fe0.8Cu0.2O3-δ has a unique fiber structure and high specific surface area, and the introduction of Cu facilitates the release of lattice oxygen, effectively increasing the oxygen vacancy content. The relaxation time distribution analysis and oxygen reduction reaction dynamics indicate that the oxygen adsorption-dissociation process is the main rate-limiting step in the oxygen reduction reaction of Pr0.5Ba0.5Fe0.8Cu0.2O3-δ electrode materials. At 700 °C, the area-specific resistance (ASR) of the symmetric cell of Pr0.5Ba0.5Fe0.8Cu0.2O3-δ fiber material is 0.071 Ω cm2, and the power density of the single cell reaches 988 mW cm−2, which shows good electrochemical output performance and long-term operational stability. The preparation of nanofiber cathodes with high specific surface area and porosity by electrospinning provides an effective strategy to enhance the electrocatalytic activity of the IT-SOFC cathode.
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用于中温固体氧化物燃料电池的新型无钴高效 Pr0.5Ba0.5Fe0.8Cu0.2O3-δ 纳米纤维阴极材料
不含钴(Co)的铁基过氧化物具有较低的热膨胀系数,可用作固体氧化物燃料电池(SOFC)的阴极,以确保与电解质的热相容性;然而,缓慢的氧还原反应(ORR)动力学阻碍了其进一步发展。本研究采用电纺丝方法和铜掺杂策略改善了 Pr0.5Ba0.5FeO3-δ 阴极的微观结构和氧还原动力学。结果表明,Pr0.5Ba0.5Fe0.8Cu0.2O3-δ具有独特的纤维结构和高比表面积,Cu的引入促进了晶格氧的释放,有效增加了氧空位含量。弛豫时间分布分析和氧还原反应动力学表明,氧吸附-解离过程是 Pr0.5Ba0.5Fe0.8Cu0.2O3-δ 电极材料氧还原反应的主要限速步骤。700 ℃时,Pr0.5Ba0.5Fe0.8Cu0.2O3-δ纤维材料对称电池的面积比电阻(ASR)为0.071 Ω cm2,单电池功率密度达到988 mW cm-2,显示出良好的电化学输出性能和长期运行稳定性。通过电纺丝制备高比表面积和高孔隙率的纳米纤维阴极为提高 IT-SOFC 阴极的电催化活性提供了一种有效的策略。
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来源期刊
Ceramics International
Ceramics International 工程技术-材料科学:硅酸盐
CiteScore
9.40
自引率
15.40%
发文量
4558
审稿时长
25 days
期刊介绍: Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties. Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour. Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.
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