H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials

Operando DRIFTS and resistance study for gas sensor applications

R. G. Pavelko, J. K. Choi, A. Urakawa, M. Yuasa, T. Kida, Kengo Shimanoe, N. Yamazoe

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

Modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) together with resistance measurements has been carried out to study water isotopic exchange on undoped SnO2 materials as a function of CO concentration. We compare two materials synthesized via hydrothermal treatment and different only in their precursors: SnO2 Ac synthesized from tin(IV) hydroxide acetate and SnO2 Cl from tin(IV) chloride pentahydrate. DRIFTS and resistance measurements were performed simultaneously in an environmental chamber at 300 °C and in a flow of humid air. The annealed materials were found to have similar particle sizes (16±7 nm), crystallite sizes (12±2 nm) and pore size distribution (9±1 nm). However, sensor tests showed notably higher responses to CO in the presence of water vapor for SnO2 Ac. Electronic effect of CO chemisorption quantitatively correlates with consumption of bridging hydroxyls on the latter surface upon increasing concentration of CO from 0 to 500 ppm in humid air. No such correlation was found for SnO2 Cl. Water desorption kinetics was found to be slower for the latter by ca. 30 % with respect to SnO2 Ac. Low activity of surface OH groups and consequently low sensor signals of SnO2 Cl were proposed to originate from traces of Cl ions found in the material after the synthesis despite negative Cl test before the hydrothermal treatment.

Original languageEnglish
Title of host publicationPhysical Chemistry of Interfaces and Nanomaterials XII
DOIs
Publication statusPublished - Dec 9 2013
EventPhysical Chemistry of Interfaces and Nanomaterials XII - San Diego, CA, United States
Duration: Aug 25 2013Aug 28 2013

Publication series

NameProceedings of SPIE - The International Society for Optical Engineering
Volume8811
ISSN (Print)0277-786X
ISSN (Electronic)1996-756X

Other

OtherPhysical Chemistry of Interfaces and Nanomaterials XII
CountryUnited States
CitySan Diego, CA
Period8/25/138/28/13

Fingerprint

Gas Sensor
Nanomaterials
Carbon Monoxide
Chemical sensors
Reflectance
Nanostructured materials
Fourier transform infrared spectroscopy
Spectroscopy
Fourier transform
tin
Infrared
reflectance
test chambers
Tin
sensors
air
gases
chemisorption
water
spectroscopy

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics
  • Computer Science Applications
  • Applied Mathematics
  • Electrical and Electronic Engineering

Cite this

Pavelko, R. G., Choi, J. K., Urakawa, A., Yuasa, M., Kida, T., Shimanoe, K., & Yamazoe, N. (2013). H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials: Operando DRIFTS and resistance study for gas sensor applications. In Physical Chemistry of Interfaces and Nanomaterials XII [881106] (Proceedings of SPIE - The International Society for Optical Engineering; Vol. 8811). https://doi.org/10.1117/12.2026594

H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials : Operando DRIFTS and resistance study for gas sensor applications. / Pavelko, R. G.; Choi, J. K.; Urakawa, A.; Yuasa, M.; Kida, T.; Shimanoe, Kengo; Yamazoe, N.

Physical Chemistry of Interfaces and Nanomaterials XII. 2013. 881106 (Proceedings of SPIE - The International Society for Optical Engineering; Vol. 8811).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Pavelko, RG, Choi, JK, Urakawa, A, Yuasa, M, Kida, T, Shimanoe, K & Yamazoe, N 2013, H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials: Operando DRIFTS and resistance study for gas sensor applications. in Physical Chemistry of Interfaces and Nanomaterials XII., 881106, Proceedings of SPIE - The International Society for Optical Engineering, vol. 8811, Physical Chemistry of Interfaces and Nanomaterials XII, San Diego, CA, United States, 8/25/13. https://doi.org/10.1117/12.2026594
Pavelko RG, Choi JK, Urakawa A, Yuasa M, Kida T, Shimanoe K et al. H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials: Operando DRIFTS and resistance study for gas sensor applications. In Physical Chemistry of Interfaces and Nanomaterials XII. 2013. 881106. (Proceedings of SPIE - The International Society for Optical Engineering). https://doi.org/10.1117/12.2026594
Pavelko, R. G. ; Choi, J. K. ; Urakawa, A. ; Yuasa, M. ; Kida, T. ; Shimanoe, Kengo ; Yamazoe, N. / H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials : Operando DRIFTS and resistance study for gas sensor applications. Physical Chemistry of Interfaces and Nanomaterials XII. 2013. (Proceedings of SPIE - The International Society for Optical Engineering).
@inproceedings{940d934de80c4b7aa85162b1a3cc6ec3,
title = "H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials: Operando DRIFTS and resistance study for gas sensor applications",
abstract = "Modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) together with resistance measurements has been carried out to study water isotopic exchange on undoped SnO2 materials as a function of CO concentration. We compare two materials synthesized via hydrothermal treatment and different only in their precursors: SnO2 Ac synthesized from tin(IV) hydroxide acetate and SnO2 Cl from tin(IV) chloride pentahydrate. DRIFTS and resistance measurements were performed simultaneously in an environmental chamber at 300 °C and in a flow of humid air. The annealed materials were found to have similar particle sizes (16±7 nm), crystallite sizes (12±2 nm) and pore size distribution (9±1 nm). However, sensor tests showed notably higher responses to CO in the presence of water vapor for SnO2 Ac. Electronic effect of CO chemisorption quantitatively correlates with consumption of bridging hydroxyls on the latter surface upon increasing concentration of CO from 0 to 500 ppm in humid air. No such correlation was found for SnO2 Cl. Water desorption kinetics was found to be slower for the latter by ca. 30 {\%} with respect to SnO2 Ac. Low activity of surface OH groups and consequently low sensor signals of SnO2 Cl were proposed to originate from traces of Cl ions found in the material after the synthesis despite negative Cl test before the hydrothermal treatment.",
author = "Pavelko, {R. G.} and Choi, {J. K.} and A. Urakawa and M. Yuasa and T. Kida and Kengo Shimanoe and N. Yamazoe",
year = "2013",
month = "12",
day = "9",
doi = "10.1117/12.2026594",
language = "English",
isbn = "9780819496614",
series = "Proceedings of SPIE - The International Society for Optical Engineering",
booktitle = "Physical Chemistry of Interfaces and Nanomaterials XII",

}

TY - GEN

T1 - H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials

T2 - Operando DRIFTS and resistance study for gas sensor applications

AU - Pavelko, R. G.

AU - Choi, J. K.

AU - Urakawa, A.

AU - Yuasa, M.

AU - Kida, T.

AU - Shimanoe, Kengo

AU - Yamazoe, N.

PY - 2013/12/9

Y1 - 2013/12/9

N2 - Modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) together with resistance measurements has been carried out to study water isotopic exchange on undoped SnO2 materials as a function of CO concentration. We compare two materials synthesized via hydrothermal treatment and different only in their precursors: SnO2 Ac synthesized from tin(IV) hydroxide acetate and SnO2 Cl from tin(IV) chloride pentahydrate. DRIFTS and resistance measurements were performed simultaneously in an environmental chamber at 300 °C and in a flow of humid air. The annealed materials were found to have similar particle sizes (16±7 nm), crystallite sizes (12±2 nm) and pore size distribution (9±1 nm). However, sensor tests showed notably higher responses to CO in the presence of water vapor for SnO2 Ac. Electronic effect of CO chemisorption quantitatively correlates with consumption of bridging hydroxyls on the latter surface upon increasing concentration of CO from 0 to 500 ppm in humid air. No such correlation was found for SnO2 Cl. Water desorption kinetics was found to be slower for the latter by ca. 30 % with respect to SnO2 Ac. Low activity of surface OH groups and consequently low sensor signals of SnO2 Cl were proposed to originate from traces of Cl ions found in the material after the synthesis despite negative Cl test before the hydrothermal treatment.

AB - Modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) together with resistance measurements has been carried out to study water isotopic exchange on undoped SnO2 materials as a function of CO concentration. We compare two materials synthesized via hydrothermal treatment and different only in their precursors: SnO2 Ac synthesized from tin(IV) hydroxide acetate and SnO2 Cl from tin(IV) chloride pentahydrate. DRIFTS and resistance measurements were performed simultaneously in an environmental chamber at 300 °C and in a flow of humid air. The annealed materials were found to have similar particle sizes (16±7 nm), crystallite sizes (12±2 nm) and pore size distribution (9±1 nm). However, sensor tests showed notably higher responses to CO in the presence of water vapor for SnO2 Ac. Electronic effect of CO chemisorption quantitatively correlates with consumption of bridging hydroxyls on the latter surface upon increasing concentration of CO from 0 to 500 ppm in humid air. No such correlation was found for SnO2 Cl. Water desorption kinetics was found to be slower for the latter by ca. 30 % with respect to SnO2 Ac. Low activity of surface OH groups and consequently low sensor signals of SnO2 Cl were proposed to originate from traces of Cl ions found in the material after the synthesis despite negative Cl test before the hydrothermal treatment.

UR - http://www.scopus.com/inward/record.url?scp=84889042539&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84889042539&partnerID=8YFLogxK

U2 - 10.1117/12.2026594

DO - 10.1117/12.2026594

M3 - Conference contribution

SN - 9780819496614

T3 - Proceedings of SPIE - The International Society for Optical Engineering

BT - Physical Chemistry of Interfaces and Nanomaterials XII

ER -