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Model-guided design of a high performance and durability Ni nanofiber/ceria matrix solid oxide fuel cell electrode

  • Mengzheng Ouyang
  • , Antonio Bertei
  • , Samuel J. Cooper
  • , Yufei Wu
  • , Paul Boldrin
  • , Xinhua Liu*
  • , Masashi Kishimoto
  • , Huizhi Wang
  • , Max Naylor Marlow
  • , Jingyi Chen
  • , Xiaolong Chen
  • , Yuhua Xia
  • , Billy Wu
  • , Nigel P. Brandon
  • *此作品的通讯作者
  • Department of Earth Science and Engineering
  • Imperial College London
  • Department of Civil and Industrial Engineering (DICI)
  • University of Pisa
  • Dyson School of Design Engineering
  • Department of Computing
  • Department of Aeronautics and Astronautics
  • Kyoto University
  • Department of Mechanical Engineering
  • Department of Chemistry
  • University of Cambridge

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

Mixed ionic electronic conductors (MIECs) have attracted increasing attention as anode materials for solid oxide fuel cells (SOFCs) and they hold great promise for lowering the operation temperature of SOFCs. However, there has been a lack of understanding of the performance-limiting factors and guidelines for rational design of composite metal-MIEC electrodes. Using a newly-developed approach based on 3D-tomography and electrochemical impedance spectroscopy, here for the first time we quantify the contribution of the dual-phase boundary (DPB) relative to the three-phase boundary (TPB) reaction pathway on real MIEC electrodes. A new design strategy is developed for Ni/gadolinium doped ceria (CGO) electrodes (a typical MIEC electrode) based on the quantitative analyses and a novel Ni/CGO fiber–matrix structure is proposed and fabricated by combining electrospinning and tape-casting methods using commercial powders. With only 11.5 vol% nickel, the designer Ni/CGO fiber–matrix electrode shows 32% and 67% lower polarization resistance than a nano-Ni impregnated CGO scaffold electrode and conventional cermet electrode respectively. The results in this paper demonstrate quantitatively using real electrode structures that enhancing DPB and hydrogen kinetics are more efficient strategies to enhance electrode performance than simply increasing TPB.

源语言英语
页(从-至)98-112
页数15
期刊Journal of Energy Chemistry
卷56
DOI
出版状态已出版 - 5月 2021

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