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Electrical reduction of perovskite electrodes for accelerating exsolution of nanoparticles

Research output: Contribution to journalArticle

Open Access Status

  • Embargoed (until 21/03/20)

Author(s)

Merika Chanthanumataporn, Jianing Hui, Xiangling Yue, Katsuyoshi Kakinuma, John T. S. Irvine, Katsunori Hanamura

School/Research organisations

Abstract

Growth of finely dispersed nanocatalysts by exsolution of metal nanoparticles from perovskite oxides under reducing conditions at elevated temperature is a promising approach of producing highly active catalytic materials. An alternative method of exsolution using an applied potential has been recently shown to potentially accelerate the exsolution process of nanoparticles that can be achieved in minutes rather than the hours required in chemical reduction. In the present study, we investigate exsolution of nanoparticles from perovskite oxides of La0.43Ca0.37Ni0.06Ti0.94O3-γ (LCTNi) and La0.43Ca0.37Ni0.03Fe0.03Ti0.94O3-γ (LCTNi-Fe) under applied potentials in carbon dioxide atmosphere. The impedance spectra of single cells measured before and after electrochemical poling at varying voltages showed that the onset of exsolution process occurred at 2 V of potential reduction. An average particle size of the exsolved nanoparticles observed after testing using a scanning electron microscopy was about 30–100 nm. The cells with the reduced electrodes exhibited desirable electrochemical performances not only in pure carbon dioxide (current density of 0.37 A cm−2 for LCTNi and 0.48 A cm−2 for LCTNi-Fe at 1.5 V) but also in dry hydrogen (0.36 W cm−2 for LCTNi and 0.43 W cm−2 for LCTNi-Fe).
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Details

Original languageEnglish
Pages (from-to)159-166
Number of pages8
JournalElectrochimica Acta
Volume306
Early online date21 Mar 2019
DOIs
Publication statusPublished - 20 May 2019

    Research areas

  • Perovskite, Exsolution, Potential reduction, CO electrolysis, Solid oxide cells

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