Ultralow-temperature CO oxidation on an In2O3-Co3O4 catalyst: a strategy to tune CO adsorption strength and oxygen activation simultaneously

Yang Lou; Xiao-Ming Cao; Jinggang Lan; Li Wang; Qiguang Dai; Yun Guo; Jian Ma; Zhenyang Zhao; Yanglong Guo; P. Hu; Guanzhong Lu

doi:10.1039/c4cc00036f

Ultralow-temperature CO oxidation on an In2O3-Co3O4 catalyst: a strategy to tune CO adsorption strength and oxygen activation simultaneously

Yang Lou, Xiao-Ming Cao, Jinggang Lan, Li Wang, Qiguang Dai, Yun Guo^*, Jian Ma, Zhenyang Zhao, Yanglong Guo, P. Hu, Guanzhong Lu

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Research output: Contribution to journal › Article › peer-review

52 Citations (Scopus)

Abstract

Highly efficient In2O3-Co3O4 catalysts were prepared for ultralow-temperature CO oxidation by simultaneously tuning the CO adsorption strength and oxygen activation over a Co3O4 surface, which could completely convert CO to CO2 at temperatures as low as -105 degrees C compared to -40 degrees C over pure Co3O4, with enhanced stability.

Original language	English
Pages (from-to)	6835-6838
Number of pages	4
Journal	Chemical Communications
Volume	50
Issue number	52
Early online date	20 Mar 2014
DOIs	https://doi.org/10.1039/c4cc00036f
Publication status	Published - 2014

Keywords

GOLD CATALYSTS
CO3O4
ORIGIN
NANOPARTICLES
TITANIA
OXIDES
BI2O3

Access to Document

10.1039/c4cc00036f

Cite this

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title = "Ultralow-temperature CO oxidation on an In2O3-Co3O4 catalyst: a strategy to tune CO adsorption strength and oxygen activation simultaneously",

abstract = "Highly efficient In2O3-Co3O4 catalysts were prepared for ultralow-temperature CO oxidation by simultaneously tuning the CO adsorption strength and oxygen activation over a Co3O4 surface, which could completely convert CO to CO2 at temperatures as low as -105 degrees C compared to -40 degrees C over pure Co3O4, with enhanced stability.",

keywords = "GOLD CATALYSTS, CO3O4, ORIGIN, NANOPARTICLES, TITANIA, OXIDES, BI2O3",

author = "Yang Lou and Xiao-Ming Cao and Jinggang Lan and Li Wang and Qiguang Dai and Yun Guo and Jian Ma and Zhenyang Zhao and Yanglong Guo and P. Hu and Guanzhong Lu",

year = "2014",

doi = "10.1039/c4cc00036f",

language = "English",

volume = "50",

pages = "6835--6838",

journal = "Chemical Communications",

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Ultralow-temperature CO oxidation on an In2O3-Co3O4 catalyst: a strategy to tune CO adsorption strength and oxygen activation simultaneously. / Lou, Yang; Cao, Xiao-Ming; Lan, Jinggang; Wang, Li; Dai, Qiguang; Guo, Yun; Ma, Jian; Zhao, Zhenyang; Guo, Yanglong; Hu, P.; Lu, Guanzhong.

In: Chemical Communications, Vol. 50, No. 52, 2014, p. 6835-6838.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Ultralow-temperature CO oxidation on an In2O3-Co3O4 catalyst: a strategy to tune CO adsorption strength and oxygen activation simultaneously

AU - Lou, Yang

AU - Cao, Xiao-Ming

AU - Lan, Jinggang

AU - Wang, Li

AU - Dai, Qiguang

AU - Guo, Yun

AU - Ma, Jian

AU - Zhao, Zhenyang

AU - Guo, Yanglong

AU - Hu, P.

AU - Lu, Guanzhong

PY - 2014

Y1 - 2014

N2 - Highly efficient In2O3-Co3O4 catalysts were prepared for ultralow-temperature CO oxidation by simultaneously tuning the CO adsorption strength and oxygen activation over a Co3O4 surface, which could completely convert CO to CO2 at temperatures as low as -105 degrees C compared to -40 degrees C over pure Co3O4, with enhanced stability.

AB - Highly efficient In2O3-Co3O4 catalysts were prepared for ultralow-temperature CO oxidation by simultaneously tuning the CO adsorption strength and oxygen activation over a Co3O4 surface, which could completely convert CO to CO2 at temperatures as low as -105 degrees C compared to -40 degrees C over pure Co3O4, with enhanced stability.

KW - GOLD CATALYSTS

KW - CO3O4

KW - ORIGIN

KW - NANOPARTICLES

KW - TITANIA

KW - OXIDES

KW - BI2O3

U2 - 10.1039/c4cc00036f

DO - 10.1039/c4cc00036f

M3 - Article

VL - 50

SP - 6835

EP - 6838

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

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