Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere

Keiji Yashiro, Shigenori Onuma, Maya Sase, Atsushi Kaimai, Takanori Otake, Hiroshige Matsumoto, Tatsuya Kawada, Junichiro Mizusaki

Research output: Contribution to journal › Conference article

3 Citations (Scopus)

Abstract

Perovskite-type oxide, La0.5Sr0.5CoO 3-δ, has large oxygen nonstoichiometry and high electrical conductivity with a large carrier concentration. The oxygen nonstoichiometry, δ, of dense La0.5Sr0.5CoO3-δ was measured in the stream of NOx-O2-N2 system at 873 to 1073 K by means of a thermogravimetric method. Small amounts of NO 2 caused large changes in oxygen nonstoichiometry. It seems probable that excessive amounts of oxygen can be incorporated into the bulk due to catalytic decomposition of NO2, and as a result, oxygen potential on the surface of the sample seems to be much higher than that of gaseous phase. EMF measurements for dense La0.6Sr0.4CoO 3-δ electrode also revealed that the oxygen potential is affected by NO2. Thus, the gas sensing mechanism of this oxide was found to relate to the change of the bulk property, especially oxygen nonstoichiometry.

Original languageEnglish
Pages (from-to)2411-2416
Number of pages6
JournalSolid State Ionics
Volume176
Issue number31-34
DOIs
Publication statusPublished - Oct 1 2005
Externally publishedYes
Event30th Symposium on Solid State Ionics in Japan -
Duration: Dec 1 2004 → Dec 3 2004

Fingerprint

Chemical potential
Oxides
Gases
Oxygen
atmospheres
oxides
shift
oxygen
gases
Perovskite
Carrier concentration
Decomposition
decomposition
Electrodes
electrical resistivity
electrodes
Electric potential

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Materials Science(all)
  • Condensed Matter Physics

Cite this

Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere. / Yashiro, Keiji; Onuma, Shigenori; Sase, Maya; Kaimai, Atsushi; Otake, Takanori; Matsumoto, Hiroshige; Kawada, Tatsuya; Mizusaki, Junichiro.

In: Solid State Ionics, Vol. 176, No. 31-34, 01.10.2005, p. 2411-2416.

Research output: Contribution to journal › Conference article

Yashiro, K, Onuma, S, Sase, M, Kaimai, A, Otake, T, Matsumoto, H, Kawada, T & Mizusaki, J 2005, 'Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere', Solid State Ionics, vol. 176, no. 31-34, pp. 2411-2416. https://doi.org/10.1016/j.ssi.2005.06.027
Yashiro K, Onuma S, Sase M, Kaimai A, Otake T, Matsumoto H et al. Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere. Solid State Ionics. 2005 Oct 1;176(31-34):2411-2416. https://doi.org/10.1016/j.ssi.2005.06.027
Yashiro, Keiji ; Onuma, Shigenori ; Sase, Maya ; Kaimai, Atsushi ; Otake, Takanori ; Matsumoto, Hiroshige ; Kawada, Tatsuya ; Mizusaki, Junichiro. / Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere. In: Solid State Ionics. 2005 ; Vol. 176, No. 31-34. pp. 2411-2416.
@article{8c5be7e14972471eae9c0c60fa752576,
title = "Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere",
abstract = "Perovskite-type oxide, La0.5Sr0.5CoO 3-δ, has large oxygen nonstoichiometry and high electrical conductivity with a large carrier concentration. The oxygen nonstoichiometry, δ, of dense La0.5Sr0.5CoO3-δ was measured in the stream of NOx-O2-N2 system at 873 to 1073 K by means of a thermogravimetric method. Small amounts of NO 2 caused large changes in oxygen nonstoichiometry. It seems probable that excessive amounts of oxygen can be incorporated into the bulk due to catalytic decomposition of NO2, and as a result, oxygen potential on the surface of the sample seems to be much higher than that of gaseous phase. EMF measurements for dense La0.6Sr0.4CoO 3-δ electrode also revealed that the oxygen potential is affected by NO2. Thus, the gas sensing mechanism of this oxide was found to relate to the change of the bulk property, especially oxygen nonstoichiometry.",
author = "Keiji Yashiro and Shigenori Onuma and Maya Sase and Atsushi Kaimai and Takanori Otake and Hiroshige Matsumoto and Tatsuya Kawada and Junichiro Mizusaki",
year = "2005",
month = "10",
day = "1",
doi = "10.1016/j.ssi.2005.06.027",
language = "English",
volume = "176",
pages = "2411--2416",
journal = "Solid State Ionics",
issn = "0167-2738",
publisher = "Elsevier",
number = "31-34",

}

TY - JOUR

T1 - Catalytic chemical potential shift on the surface of nonstoichiometric oxides under non-equilibrium gas atmosphere

AU - Yashiro, Keiji

AU - Onuma, Shigenori

AU - Sase, Maya

AU - Kaimai, Atsushi

AU - Otake, Takanori

AU - Matsumoto, Hiroshige

AU - Kawada, Tatsuya

AU - Mizusaki, Junichiro

PY - 2005/10/1

Y1 - 2005/10/1

N2 - Perovskite-type oxide, La0.5Sr0.5CoO 3-δ, has large oxygen nonstoichiometry and high electrical conductivity with a large carrier concentration. The oxygen nonstoichiometry, δ, of dense La0.5Sr0.5CoO3-δ was measured in the stream of NOx-O2-N2 system at 873 to 1073 K by means of a thermogravimetric method. Small amounts of NO 2 caused large changes in oxygen nonstoichiometry. It seems probable that excessive amounts of oxygen can be incorporated into the bulk due to catalytic decomposition of NO2, and as a result, oxygen potential on the surface of the sample seems to be much higher than that of gaseous phase. EMF measurements for dense La0.6Sr0.4CoO 3-δ electrode also revealed that the oxygen potential is affected by NO2. Thus, the gas sensing mechanism of this oxide was found to relate to the change of the bulk property, especially oxygen nonstoichiometry.

AB - Perovskite-type oxide, La0.5Sr0.5CoO 3-δ, has large oxygen nonstoichiometry and high electrical conductivity with a large carrier concentration. The oxygen nonstoichiometry, δ, of dense La0.5Sr0.5CoO3-δ was measured in the stream of NOx-O2-N2 system at 873 to 1073 K by means of a thermogravimetric method. Small amounts of NO 2 caused large changes in oxygen nonstoichiometry. It seems probable that excessive amounts of oxygen can be incorporated into the bulk due to catalytic decomposition of NO2, and as a result, oxygen potential on the surface of the sample seems to be much higher than that of gaseous phase. EMF measurements for dense La0.6Sr0.4CoO 3-δ electrode also revealed that the oxygen potential is affected by NO2. Thus, the gas sensing mechanism of this oxide was found to relate to the change of the bulk property, especially oxygen nonstoichiometry.

UR - http://www.scopus.com/inward/record.url?scp=25444503982&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=25444503982&partnerID=8YFLogxK

U2 - 10.1016/j.ssi.2005.06.027

DO - 10.1016/j.ssi.2005.06.027

M3 - Conference article

AN - SCOPUS:25444503982

VL - 176

SP - 2411

EP - 2416

JO - Solid State Ionics

JF - Solid State Ionics

SN - 0167-2738

IS - 31-34

ER -

Access to Document