Is Fluorine Incorporation in the La0.6Sr0.4Co0.2Fe0.8O3-δ Improving Its Electrochemical Behavior for Solid Oxide Cells Applications?

被引:5
作者
Shen, Zonghao [1 ,2 ]
Bassat, Jean-Marc [1 ]
Fourcade, Sebastien [1 ]
Demourgues, Alain [1 ]
Durand, Etienne [1 ]
Teule-Gay, Lionel [1 ]
Duttine, Mathieu [1 ]
Gamon, Jacinthe [1 ]
机构
[1] Univ Bordeaux, France Univ, CNRS, Bordeaux INP,ICMCB,UMR 5026, F-33600 Pessac, France
[2] Grenoble Alpes, CNRS, Grenoble INP, LMGP, F-38000 Grenoble, France
关键词
fluorine doping; LSCF; mixed anions; polarization resistance; solid oxide cell; OXYGEN; FUEL; PHASES; PEROVSKITES; OXYFLUORIDE; PERFORMANCE; KINETICS; CATHODE;
D O I
10.1002/aenm.202401518
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
F-doped La0.6Sr0.4Co0.2Fe0.8O3-x-delta Fx (LSCFFx, x = 0.05, 0.10, and 0.20) materials are evaluated as oxygen electrodes for solid oxide fuel and electrolyser cell application. Materials have been prepared via low-temperature topotactic route by fluorination of the parent oxide with polyvinylidene fluorine (PVDF). A decrease in the polarisation resistance (R-p) is observed for the "LSCFFx" symmetric cells. However, the improved electrochemical behavior for the symmetric cells cannot be explained by the presence of fluorine, as post mortem chemical analysis shows that fluorine is absent from the materials after the calcination treatment, contradicting previous results from the literature and calling for deeper understanding. The presence of fluorine is proved to result in a sluggish surface exchange rate compared with the LSCF oxide via pulsed isotopic exchange technique. Despite the absence of fluorine in the fabricated symmetric cell, annealing with PVDF at low temperatures prior to the electrode fabrication is proven to be a beneficial step to improve the electrochemical performance of LSCF material with applications for solid oxide cells. Studies with room temperature X-ray diffraction, X-ray photoelectron spectroscopy, and M & ouml;ssbauer spectroscopy suggest that increased oxygen vacancy concentration, structural disorder and changes in the cobalt/iron valence state distribution are potential explanations for the reduced R-p.
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页数:16
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