An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells

The target of this work is to develop advanced electrode materials with excellent performance compared to conventional cathodes. Cobalt-free Ruddlesden−Popper oxides Sr<sub>3</sub>Fe<sub>2−<i>x</i></sub>Cu<i><sub>x</sub></i>O<sub>7−&l...

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Autores principales: Longsheng Peng, Qiang Li, Liping Sun, Hui Zhao
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:834d5a391959421f9c01bb5997696c352021-11-25T17:06:48ZAn Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells10.3390/catal111114002073-4344https://doaj.org/article/834d5a391959421f9c01bb5997696c352021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4344/11/11/1400https://doaj.org/toc/2073-4344The target of this work is to develop advanced electrode materials with excellent performance compared to conventional cathodes. Cobalt-free Ruddlesden−Popper oxides Sr<sub>3</sub>Fe<sub>2−<i>x</i></sub>Cu<i><sub>x</sub></i>O<sub>7−</sub><i><sub>δ</sub></i> (SFC<i>x</i>, <i>x</i> = 0, 0.1, 0.2) were successfully synthesized and assessed as cathode materials for solid oxide fuel cells (SOFCs). Herein, a Cu-doping strategy is shown to increase the electrical conductivity and improve the electrochemical performance of the pristine Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i>. Among all the cathode materials, the Sr<sub>3</sub>Fe<sub>1.9</sub>Cu<sub>0.1</sub>O<sub>7−</sub><i><sub>δ</sub></i> (SFC10) cathode exhibits the best electrocatalytic activity for oxygen reduction reaction (ORR). The polarization resistance is 0.11 Ω cm<sup>2</sup> and the peak power density of the single-cell with an SFC10 cathode reaches 955 mW cm<sup>−2</sup> at 700 °C, a measurement comparable to cobalt-based electrodes. The excellent performance is owed to favorable oxygen surface exchange capabilities and larger oxygen vacancy concentrations at elevated temperatures. Moreover, the electrochemical impedance spectra and distribution of relaxation time results indicate that the charge transfer process at the triple-phase boundary is the rate-limiting step for ORR on the electrode. This work provides an effective strategy for designing novel cathode electrocatalysts for SOFCs.Longsheng PengQiang LiLiping SunHui ZhaoMDPI AGarticlesolid oxide fuel cellscathode materialRuddlesden−Popper oxideselectrochemical performanceChemical technologyTP1-1185ChemistryQD1-999ENCatalysts, Vol 11, Iss 1400, p 1400 (2021)
institution DOAJ
collection DOAJ
language EN
topic solid oxide fuel cells
cathode material
Ruddlesden−Popper oxides
electrochemical performance
Chemical technology
TP1-1185
Chemistry
QD1-999
spellingShingle solid oxide fuel cells
cathode material
Ruddlesden−Popper oxides
electrochemical performance
Chemical technology
TP1-1185
Chemistry
QD1-999
Longsheng Peng
Qiang Li
Liping Sun
Hui Zhao
An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
description The target of this work is to develop advanced electrode materials with excellent performance compared to conventional cathodes. Cobalt-free Ruddlesden−Popper oxides Sr<sub>3</sub>Fe<sub>2−<i>x</i></sub>Cu<i><sub>x</sub></i>O<sub>7−</sub><i><sub>δ</sub></i> (SFC<i>x</i>, <i>x</i> = 0, 0.1, 0.2) were successfully synthesized and assessed as cathode materials for solid oxide fuel cells (SOFCs). Herein, a Cu-doping strategy is shown to increase the electrical conductivity and improve the electrochemical performance of the pristine Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i>. Among all the cathode materials, the Sr<sub>3</sub>Fe<sub>1.9</sub>Cu<sub>0.1</sub>O<sub>7−</sub><i><sub>δ</sub></i> (SFC10) cathode exhibits the best electrocatalytic activity for oxygen reduction reaction (ORR). The polarization resistance is 0.11 Ω cm<sup>2</sup> and the peak power density of the single-cell with an SFC10 cathode reaches 955 mW cm<sup>−2</sup> at 700 °C, a measurement comparable to cobalt-based electrodes. The excellent performance is owed to favorable oxygen surface exchange capabilities and larger oxygen vacancy concentrations at elevated temperatures. Moreover, the electrochemical impedance spectra and distribution of relaxation time results indicate that the charge transfer process at the triple-phase boundary is the rate-limiting step for ORR on the electrode. This work provides an effective strategy for designing novel cathode electrocatalysts for SOFCs.
format article
author Longsheng Peng
Qiang Li
Liping Sun
Hui Zhao
author_facet Longsheng Peng
Qiang Li
Liping Sun
Hui Zhao
author_sort Longsheng Peng
title An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
title_short An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
title_full An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
title_fullStr An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
title_full_unstemmed An Effective Strategy to Enhance the Electrocatalytic Activity of Ruddlesden−Popper Oxides Sr<sub>3</sub>Fe<sub>2</sub>O<sub>7−</sub><i><sub>δ</sub></i> Electrodes for Solid Oxide Fuel Cells
title_sort effective strategy to enhance the electrocatalytic activity of ruddlesden−popper oxides sr<sub>3</sub>fe<sub>2</sub>o<sub>7−</sub><i><sub>δ</sub></i> electrodes for solid oxide fuel cells
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/834d5a391959421f9c01bb5997696c35
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