Comparison of a solid oxide cell with nickel/gadolinium-doped ceria fuel electrode during operation with hydrogen/steam and carbon monoxide/carbon dioxide
Cedric Grosselindemann, Felix Kullmann, Tibor Lehnert, Oliver Fritz, Franz-Martin Fuchs, André Weber
{"title":"Comparison of a solid oxide cell with nickel/gadolinium-doped ceria fuel electrode during operation with hydrogen/steam and carbon monoxide/carbon dioxide","authors":"Cedric Grosselindemann, Felix Kullmann, Tibor Lehnert, Oliver Fritz, Franz-Martin Fuchs, André Weber","doi":"10.1002/fuce.202300060","DOIUrl":null,"url":null,"abstract":"Solid oxide cells (SOCs) offer the possibility to operate on hydrogen/steam (H<sub>2</sub>/H<sub>2</sub>O), carbon monoxide/carbon dioxide (CO/CO<sub>2</sub>), and mixtures thereof in the fuel cell as well as in the electrolyzer mode. In this study, the electrochemical processes in an electrolyte-supported SOC exhibiting a La<sub>w</sub> Sr<sub>x</sub> Co<sub>y</sub> Fe<sub>z</sub> O<sub>(3-δ)</sub> air electrode and a nickel/gadolinium-doped ceria (Ni/CGO) fuel electrode (FE) were analyzed by electrochemical impedance spectroscopy, and the subsequent impedance data analysis by the distribution of relaxation times for CO/CO<sub>2</sub> fuel mixtures. A physicochemical equivalent circuit model was fitted to the measured spectra. With the help of the extracted parameters, a zero-dimensional direct current cell model was parametrized to simulate the current-voltage behavior of the cell. This approach, previously implemented for H<sub>2</sub>/H<sub>2</sub>O fuel mixtures, is extended toward CO/CO<sub>2</sub> fuels. It will be shown that the same model – with adapted parameters for the FE – can be applied. A comparison of measured and simulated current-voltage curves showed an excellent agreement for both fuels and operating modes (solid oxide fuel cell/solid oxide electrolyzer cell). Simulations reveal that there is nearly no performance difference between H<sub>2</sub>O and CO<sub>2</sub> electrolysis for the electrolyte-supported cell with Ni/CGO FE in comparison to an anode-supported cell with Ni/yttria-stabilized zirconia FE.","PeriodicalId":12566,"journal":{"name":"Fuel Cells","volume":"3 1","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2023-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Cells","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/fuce.202300060","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
Solid oxide cells (SOCs) offer the possibility to operate on hydrogen/steam (H2/H2O), carbon monoxide/carbon dioxide (CO/CO2), and mixtures thereof in the fuel cell as well as in the electrolyzer mode. In this study, the electrochemical processes in an electrolyte-supported SOC exhibiting a Law Srx Coy Fez O(3-δ) air electrode and a nickel/gadolinium-doped ceria (Ni/CGO) fuel electrode (FE) were analyzed by electrochemical impedance spectroscopy, and the subsequent impedance data analysis by the distribution of relaxation times for CO/CO2 fuel mixtures. A physicochemical equivalent circuit model was fitted to the measured spectra. With the help of the extracted parameters, a zero-dimensional direct current cell model was parametrized to simulate the current-voltage behavior of the cell. This approach, previously implemented for H2/H2O fuel mixtures, is extended toward CO/CO2 fuels. It will be shown that the same model – with adapted parameters for the FE – can be applied. A comparison of measured and simulated current-voltage curves showed an excellent agreement for both fuels and operating modes (solid oxide fuel cell/solid oxide electrolyzer cell). Simulations reveal that there is nearly no performance difference between H2O and CO2 electrolysis for the electrolyte-supported cell with Ni/CGO FE in comparison to an anode-supported cell with Ni/yttria-stabilized zirconia FE.
期刊介绍:
This journal is only available online from 2011 onwards.
Fuel Cells — From Fundamentals to Systems publishes on all aspects of fuel cells, ranging from their molecular basis to their applications in systems such as power plants, road vehicles and power sources in portables.
Fuel Cells is a platform for scientific exchange in a diverse interdisciplinary field. All related work in
-chemistry-
materials science-
physics-
chemical engineering-
electrical engineering-
mechanical engineering-
is included.
Fuel Cells—From Fundamentals to Systems has an International Editorial Board and Editorial Advisory Board, with each Editor being a renowned expert representing a key discipline in the field from either a distinguished academic institution or one of the globally leading companies.
Fuel Cells—From Fundamentals to Systems is designed to meet the needs of scientists and engineers who are actively working in the field. Until now, information on materials, stack technology and system approaches has been dispersed over a number of traditional scientific journals dedicated to classical disciplines such as electrochemistry, materials science or power technology.
Fuel Cells—From Fundamentals to Systems concentrates on the publication of peer-reviewed original research papers and reviews.