4.8 Review

Perovskite Cathode Materials for Low-Temperature Solid Oxide Fuel Cells: Fundamentals to Optimization

Journal

ELECTROCHEMICAL ENERGY REVIEWS
Volume 5, Issue 2, Pages 263-311

Publisher

SPRINGERNATURE
DOI: 10.1007/s41918-021-00098-3

Keywords

Oxygen reduction reaction; Solid oxide fuel cell; Perovskite; Cathode; Electrocatalysis

Funding

  1. China Scholarship Council (CSC)
  2. HBIS Group
  3. Australian Research Council (ARC) Linkage Project [LP160101729]
  4. ARC Discovery Projects [DP170104660, DP190101782]

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Acceleration of the oxygen reduction reaction at the cathode is crucial for low-temperature solid oxide fuel cells. Understanding the interactions between surface and bulk of the cathode materials is important for electrode kinetics and overall efficacy. Future research directions include investigating the role of oxygen vacancy, rational modulation of surface-bulk interactions, and the use of advanced fabrication techniques.
Acceleration of the oxygen reduction reaction at the cathode is paramount in the development of low-temperature solid oxide fuel cells. At low operating temperatures between 450 and 600 degrees C, the interactions between the surface and the bulk of the cathode materials greatly impact the electrode kinetics and consequently determine the overall efficacy and long-term stability of the fuel cells. This review will provide an overview of the recent progress in the understanding of surface-bulk interactions in perovskite oxides as well as their impact on cathode reactivity and stability. This review will also summarize current strategies in the development of cathode materials through bulk doping and surface functionalization. In addition, this review will highlight the roles of surface segregation in the mediation of surface and bulk interactions, which have profound impacts on the properties of cathode surfaces and the bulk and therefore overall cathode performance. Although trade-offs between reactivity and stability commonly exist in terms of catalyst design, opportunities also exist in attaining optimal cathode performance through the modulation of both cathode surfaces and bulk using combined strategies. This review will conclude with future research directions involving investigations into the role of oxygen vacancy and mobility in catalysis, the rational modulation of surface-bulk interactions and the use of advanced fabrication techniques, all of which can lead to optimized cathode performance. [GRAPHICS] .

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