4.8 Article

Quantifying the performance evolution of solid oxide fuel cells during initial aging process

Journal

JOURNAL OF POWER SOURCES
Volume 510, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2021.230432

Keywords

Solid oxide fuel cell; Degradation mechanism; Electrochemical impedance spectroscopy; Distribution of relaxation time; Equivalent circuit model

Funding

  1. National Key R&D Program of China [2018YFB1502203]
  2. Tsinghua University Initiative Scientific Research Program [20193080046]

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This study investigates the degradation mechanisms in solid oxide fuel cells (SOFCs) during initial aging process, with a focus on anode charge transfer reactions and ionic transport being the main contributors to the voltage degradation. The deterioration of the anode/electrolyte interface caused by nickel redistribution is identified as the dominant degradation mechanism.
Detailed explanation and reliable quantification of the numerous degradation mechanisms contained in solid oxide fuel cells (SOFCs) are key issues to improve their durability. Although electrochemical impedance spectroscopy (EIS) has been widely used to unfold the complex and coupled physical/chemical processes, there are still some concerns with respect to the measurement and analysis procedures. In this study, an industrial-size cell (10 x 10 cm(2)) is tested to clarify the evolution of electrochemical characteristics during initial-stage operation, including 5 h of anode reduction, 32 h of activation process and 40 h of initial aging process. Detailed analysis of EIS measured under different DC bias is implemented through distribution of relaxation times (DRT) and subsequent equivalent circuit model (ECM) fitting to identify the contributions of individual processes to the rapid performance degradation during initial aging process. It is found that the deterioration of anode charge transfer reactions and ionic transport jointly causes more than 60% of the voltage degradation, followed by the O-2 surface exchange kinetics coupled with O2- diffusion (17.3%), and then the anode gas conversion (13%). The microstructure deterioration of anode/electrolyte interface caused by Ni redistribution is regarded as the dominant degradation mechanism during initial aging process. A fast Ni migration mechanism is proposed to explain the observable Ni depletion in the anode functional layer, which is verified by detailed post-test characterization.

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