The ionic conductivity of the interlayer in the intermediate temperature solid oxide electrolysis cell (IT-SOEC) affects the polarization resistance of the oxygen electrode. Improving the ionic conductivity of the interlayer can improve the performance of the oxygen electrode. In this work, the ionic conductivity of a samarium-doped ceria (SDC) interlayer is improved by doping the transition metal oxide FeO. The experimental results show that the oxygen electrode polarization resistance of the symmetrical cell based on the SDC-FeO interlayer is 0.09 Ω cm at 800 °C and under the open circuit voltage, which is obviously lower than that of the symmetrical cell based on an SDC interlayer (0.22 Ω cm). Besides, the electrolysis current of the SOEC based on the SDC-FeO interlayer is 0.5 A cm at 800 °C and 1.5 V, which is higher than that of the SOEC based on the SDC interlayer (0.3 A cm). The above results show that improving the ionic conductivity of the SDC interlayer in the SOEC by doping FeO can reduce the polarization resistance of the oxygen electrode and enhance the performance of the SOEC. Thus, this work provides an effective way for improving the performance of the SDC interlayer in the IT-SOEC.
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http://dx.doi.org/10.1039/d1ra04361g | DOI Listing |
RSC Adv
September 2021
College of Physics Science and Technology, Shenyang Normal University Shenyang 110034 China
The ionic conductivity of the interlayer in the intermediate temperature solid oxide electrolysis cell (IT-SOEC) affects the polarization resistance of the oxygen electrode. Improving the ionic conductivity of the interlayer can improve the performance of the oxygen electrode. In this work, the ionic conductivity of a samarium-doped ceria (SDC) interlayer is improved by doping the transition metal oxide FeO.
View Article and Find Full Text PDFSci Rep
November 2021
Department of Biological and Chemical Engineering, Carbon Dioxide Activation Center (CADIAC), Aarhus University, Åbogade 40, 8200, Aarhus N, Denmark.
We present the synthesis, crystal structures and optical properties of three thiostannates prepared by using 1-(2-aminoethyl)piperazine (AEPz) as structure directing agent. Two of the thiostannates are layered materials (AEPz-SnS-1 and AEPz:EtOH-SnS-1) consisting of [SnS] sheets with organic cations located in-between. The third compound is a molecular thiostannate (SnS(AEPzH)) composed of dimeric SnS and AEPzH.
View Article and Find Full Text PDFPolymers (Basel)
March 2021
Grupo de Diseño de Productos y Procesos (GDPP), Department of Chemical and Food Engineering, Universidad de los Andes, CR 1 18a 12, Bogotá 111711, Colombia.
Nowadays the use of natural fiber composites has gained significant interest due to their low density, high availability, and low cost. The present study explores the development of sustainable 3D printing filaments based on rice husk (RH), an agricultural residue, and recycled polypropylene (rPP) and the influence of fiber weight ratio on physical, thermal, mechanical, and morphological properties of 3D printing parts. Thermogravimetric analysis revealed that the composite's degradation process started earlier than for the neat rPP due to the lignocellulosic fiber components.
View Article and Find Full Text PDFDalton Trans
August 2020
Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing 100875, China.
In this work, we demonstrate the tunable luminescence of newly synthesized SDC/OS Mg/Al-LDH composites (SDC is 4,4'-stilbenedicarboxylic acid; OS is 1-octanesulfonic acid sodium; LDH is layered double hydroxide) and their application in fluorescence sensing to detect Fe(iii) ions. Through an ion-exchange method, the SDC and OS anions with changed molar ratios are intercalated into the LDH interlayers to obtain composites of SDCOS-LDH (x = 0.02, 0.
View Article and Find Full Text PDFNanoscale
November 2019
School of Chemical Sciences, University of Chinese Academy of Sciences, 19 Yuquan Road, Shijingshan District, Beijing, 100049, PR China.
Molybdenum disulfide (MoS) is a potential earth-abundant electrocatalyst for the hydrogen evolution reaction (HER), but the lack of in-depth understanding of its intrinsic activity still impedes the further optimization and design of MoS-based electrocatalysts. Herein, we report a facile in situ hydrothermal synthetic method to prepare vertical MoS arrays grown on guar gum-derived carbon aerogels (GCA), termed MoS@GCA. The obtained well-assembled MoS@GCA architectures consist of uniform, few-layered and S-edge-rich MoS nanoflakes with a length of approximately 100 nm, which effectively prevent the inherent stacking among MoS layers and connect the charge transfer path between interlayers, thus endowing MoS@GCA with a huge number of active sites and high conductivity.
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