{"title":"Enhanced performance of Sr2Fe1.5Mo0.5O6-δ electrode by infiltrating dual functional barium carbonate nanoparticles in symmetrical SOFCs","authors":"Wei Tang, Yingwei Lu, Pengqi Chen, Tao Hong, Dong Tian, Shiyue Zhu, Jigui Cheng","doi":"10.1007/s10008-024-06125-9","DOIUrl":null,"url":null,"abstract":"<div><p>In solid oxide fuel cell (SOFC) electrode catalyst, the reaction in cathode and anode involves different reactions that require diverse catalytic materials. In this work, BaCO<sub>3</sub> as a non-ionic/electronic conductor was infiltrated into Sr<sub>2</sub>Fe<sub>1.5</sub>Mo<sub>0.5</sub>O<sub>6-δ</sub> (SFM) electrode in symmetrical SOFC. The oxygen reduction reaction in SFM cathode could be enhanced when infiltrated with BaCO<sub>3</sub>, as area-specific resistance (ASR) was reduced from 0.33 to 0.15 Ωcm<sup>2</sup> at 700 °C. The 0.42 Ωcm<sup>2</sup> ASR values of SFM anode are reduced to 0.35 Ωcm<sup>2</sup>. The performance improvement is directly related with the loading weight of BaCO<sub>3</sub>, which is actually the surface coverage of BaCO<sub>3</sub> on SFM electrode frame. And the oxygen surface exchange coefficient of SFM cathode is improved from 4.8 × 10<sup>−5</sup> to 10.5 × 10<sup>−5</sup> cms<sup>−1</sup> at 800 °C, but the hydrogen oxidation rate of SFM anode is slightly increased, which is consistent with the infiltrated SFM anode. For a full cell with BaCO<sub>3</sub> infiltrated SFM as cathode and anode, the power density is 0.81 Wcm<sup>−2</sup> that is 44% higher than the bare SFM electrode at 800 °C and remains stable at 0.64 Acm<sup>−2</sup> for the 200 h test. As a cheap and extensive synergistic catalyst for electrode reaction, barium carbonate shows great application potential in SOFC.</p></div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"29 5","pages":"1743 - 1754"},"PeriodicalIF":2.6000,"publicationDate":"2024-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Electrochemistry","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10008-024-06125-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
In solid oxide fuel cell (SOFC) electrode catalyst, the reaction in cathode and anode involves different reactions that require diverse catalytic materials. In this work, BaCO3 as a non-ionic/electronic conductor was infiltrated into Sr2Fe1.5Mo0.5O6-δ (SFM) electrode in symmetrical SOFC. The oxygen reduction reaction in SFM cathode could be enhanced when infiltrated with BaCO3, as area-specific resistance (ASR) was reduced from 0.33 to 0.15 Ωcm2 at 700 °C. The 0.42 Ωcm2 ASR values of SFM anode are reduced to 0.35 Ωcm2. The performance improvement is directly related with the loading weight of BaCO3, which is actually the surface coverage of BaCO3 on SFM electrode frame. And the oxygen surface exchange coefficient of SFM cathode is improved from 4.8 × 10−5 to 10.5 × 10−5 cms−1 at 800 °C, but the hydrogen oxidation rate of SFM anode is slightly increased, which is consistent with the infiltrated SFM anode. For a full cell with BaCO3 infiltrated SFM as cathode and anode, the power density is 0.81 Wcm−2 that is 44% higher than the bare SFM electrode at 800 °C and remains stable at 0.64 Acm−2 for the 200 h test. As a cheap and extensive synergistic catalyst for electrode reaction, barium carbonate shows great application potential in SOFC.
期刊介绍:
The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.