V. E. Tagarelli, J. Vega-Castillo, A. Montenegro-Hernández
{"title":"Chemical compatibility of solid oxide fuel cell air electrode Pr4Ni3O10±δ with commercial electrolytes","authors":"V. E. Tagarelli, J. Vega-Castillo, A. Montenegro-Hernández","doi":"10.1002/fuce.202300176","DOIUrl":null,"url":null,"abstract":"<p>The chemical reactivity between Pr<sub>4</sub>Ni<sub>3</sub>O<sub>10±δ</sub> (3-PNO) electrodes and Y<sub>0.08</sub>Zr<sub>0.92</sub>O<sub>1.96</sub> (YSZ), Ce<sub>0.9</sub>Gd<sub>0.1</sub>O<sub>1.95</sub> (GDC), and La<sub>0.9</sub>Sr<sub>0.1</sub>Ga<sub>0.8</sub>Mg<sub>0.2</sub>O<sub>2.85</sub> (LSGM) electrolytes was analyzed by electrochemical impedance spectroscopy and X-ray diffraction. 3-PNO powders were synthesized by two different chemical routes, one of them uses hexamethylenetetramine (HMTA) as a complexing agent (route A) while the other citrates (route B). The samples observed by scanning electron microscopy presented different microstructures; route A powders present small submicronic grains with an open microstructure while route B powders are formed by larger well-connected grains. The polarization resistance (<i>R</i><sub>P</sub>) values for 3-PNO/YSZ cells are one order of magnitude higher than those of 3-PNO/GDC and 3-PNO/LSGM cells. The <i>R</i><sub>P</sub> for both cells 3-PNO/GDC and 3-PNO/LSGM and its evolution in time suggest that chemical reactivity takes place during the adhesion treatment and electrochemical measurements. The microstructure plays a crucial role in <i>R</i><sub>P</sub> and the degradation rate; 3-PNO obtained by route A (3-PNO-HMTA) exhibits the best electrochemical performance since these powders present a well-loose morphology and a large exposed area. However, this fact makes them active chemically, so the increase of <i>R</i><sub>P</sub> with time is slower for 3-PNO electrodes prepared by route B (3-PNO-Cit), since the rate of chemical reactivity with the electrolyte is slower.</p>","PeriodicalId":12566,"journal":{"name":"Fuel Cells","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Cells","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/fuce.202300176","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
The chemical reactivity between Pr4Ni3O10±δ (3-PNO) electrodes and Y0.08Zr0.92O1.96 (YSZ), Ce0.9Gd0.1O1.95 (GDC), and La0.9Sr0.1Ga0.8Mg0.2O2.85 (LSGM) electrolytes was analyzed by electrochemical impedance spectroscopy and X-ray diffraction. 3-PNO powders were synthesized by two different chemical routes, one of them uses hexamethylenetetramine (HMTA) as a complexing agent (route A) while the other citrates (route B). The samples observed by scanning electron microscopy presented different microstructures; route A powders present small submicronic grains with an open microstructure while route B powders are formed by larger well-connected grains. The polarization resistance (RP) values for 3-PNO/YSZ cells are one order of magnitude higher than those of 3-PNO/GDC and 3-PNO/LSGM cells. The RP for both cells 3-PNO/GDC and 3-PNO/LSGM and its evolution in time suggest that chemical reactivity takes place during the adhesion treatment and electrochemical measurements. The microstructure plays a crucial role in RP and the degradation rate; 3-PNO obtained by route A (3-PNO-HMTA) exhibits the best electrochemical performance since these powders present a well-loose morphology and a large exposed area. However, this fact makes them active chemically, so the increase of RP with time is slower for 3-PNO electrodes prepared by route B (3-PNO-Cit), since the rate of chemical reactivity with the electrolyte is slower.
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