Volume 8, Issue 3 1901213
Full Paper

Selective Reduction of Oxygen on Non-Noble Metal Copper Nanocatalysts

Andrew N. Kuhn

Andrew N. Kuhn

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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Yanling Ma

Yanling Ma

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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Cheng Zhang

Cheng Zhang

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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Zhitao Chen

Zhitao Chen

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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Mingyan Liu

Mingyan Liu

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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Yongqi Lu

Yongqi Lu

Illinois State Geological Survey, University of Illinois at Urbana-Champaign, 615 East Peabody Drive, Champaign, IL, 61820 USA

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Hong Yang

Corresponding Author

Hong Yang

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, MC-712, 600 South Mathews Avenue, Urbana, IL, 61801 USA

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First published: 03 January 2020
Citations: 5

Abstract

Efficient removal of molecular oxygen (O2) from flue gas is necessary to capture and utilize carbon dioxide (CO2) from fossil-fuel sources. Herein, the catalytic reduction of O2 in simulated flue gases using alumina-supported copper (Cu) nanostructures is presented. The Cu catalyst outperformed conventional palladium systems for the selectivity toward CO2 over carbon monoxide (CO). Varying the reactant feed ratio can lead to structural rearrangements at the surface of Cu nanoparticles, resulting in significant differences in catalytic activity. Under optimal conditions, a favorable Cu@CuOx core-shell structure is observed to exhibit both excellent activity and selectivity to CO2. The simulated flue gas is purified from 85% to >99.9% (v/v) CO2 after passing the catalytic system. The catalyst also exhibits high stability, showing only ≈0.1% drop in CO2 after 10 h on stream. This design marks progress toward the sequestration of CO2 and the development of non-noble catalysts by tuning their dynamic nanostructures under controllable reaction conditions.

Conflict of Interest

The authors declare no conflict of interest.

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