4.8 Article

Performance enhancement of molten carbonate-based direct carbon fuel cell (MC-DCFC) via adding mixed ionic-electronic conductors into Ni anode catalyst layer

Journal

JOURNAL OF POWER SOURCES
Volume 386, Issue -, Pages 28-33

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2018.01.078

Keywords

Direct carbon fuel cells; Lanthanum strontium cobalt ferrite; Mixed ionic-electronic conductors; Ni anode catalyst layer; Maximized triple phase boundaries

Funding

  1. National Research Foundation [2015R1A2A1A10056156, 2015M1A2A2056556, 2017R1A4A1015533]
  2. Nano-Convergence Foundation [R201500910]
  3. Korea Institute of Energy Technology Evaluation and Planning - Korea government [20153010041750]
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [20153010041750] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2015R1A2A1A10056156] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A high overpotential in the anode of Direct Carbon Fuel Cells (DCFC) is ascribed to the sluggish kinetics of solid fuel oxidation. In this study, we demonstrate a unique approach to enhance the performance of molten-carbonate electrolyte based DCFC (MC-DCFC) by decreasing a serious polarization loss at the anode side; a simple addition of lanthanum strontium cobalt ferrite (LSCF) having a function of mixed ionic-electronic conductors (MIEC) into the Ni anode catalyst layer. Ni:LSCF = 1:1 showed markedly enhanced peak power density of 111 mW/cm(2), approximately two-fold higher value than that for the anode using solely Ni and one of the best record in the literature value using carbon black fuel without any contribution of generated syngas oxidation. As can be noted from the electrochemical impedance spectroscopy data, the ohmic and the charge transfer resistance of the anode was markedly decreased owing to the high ionic-electronic conductivity of the MIECs. Furthermore, the enhanced performance can be also attributed to the maximized TPBs (triple phase boundaries) that participate in the carbon oxidation reaction. Based on the results, we suggest that the addition of MIEC materials into the Ni anode catalyst layer is a promising approach to improve the performance of MC-DCFC.

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