Barium Carbonate Nanoparticles as Synergistic Catalysts for the Oxygen Reduction Reaction on La0.6Sr0.4Co0.2Fe0.8O3−δ Solid‐Oxide Fuel Cell Cathodes

材料科学 碳酸钡 电化学 电极 纳米颗粒 极化(电化学) 氧化物 催化作用 氧气 氧化钡 电导率 化学工程 无机化学 纳米技术 化学 物理化学 冶金 原材料 有机化学 工程类 生物化学
作者
Tao Hong,Kyle S. Brinkman,Changrong Xia
出处
期刊:ChemElectroChem [Wiley]
卷期号:3 (5): 805-813 被引量:40
标识
DOI:10.1002/celc.201500529
摘要

Abstract Barium carbonate (BaCO 3 ) nanoparticles have been demonstrated to have excellent synergistic catalytic activity for the oxygen reduction reaction on La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3− δ (LSCF) and LSCF‐SDC (SDC=Sm 0.2 Ce 0.8 O 1.9 ), which are typical mixed conducting electrode materials for solid‐oxide fuel cells (SOFCs). The BaCO 3 nanoparticles were deposited into the porous electrodes through an infiltration/impregnation method with barium acetate as the precursor. Electrochemical impedance analysis indicated that BaCO 3 dramatically reduced the resistance associated with the low‐frequency response, which suggests that BaCO 3 greatly enhances the kinetics of the surface reaction process. Electrical conductivity relaxation experiments revealed that BaCO 3 particles enlarged the oxygen chemical surface exchange coefficient by a factor of up to eight. As a result, the interfacial polarization resistance of both the LSCF and LSCF‐SDC electrodes was greatly reduced, from 0.28 and 0.13 to 0.12 and 0.047 Ω cm 2 , respectively, at 700 °C. In addition, the single‐cell performance was also improved and demonstrated peak power density from 0.66 and 0.71 to 0.73 and 0.81 W cm 2 for the LSCF and LSCF‐SDC cathodes, respectively, at 700 °C. The LSCF electrode infiltrated with BaCO 3 nanoparticles also exhibited higher stability than the bare LSCF electrode in tests conducted under typical SOFC conditions for over 340 h of operation.
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