Synthesis and Evaluation of Cu@ZnO Core@Shell Nanowires for Use in the Carbon Dioxide Thermal Reduction Reaction

Copper-based core@shell nanomaterials are of interest for the catalytic hydrogenation of carbon dioxide toward value-added products. In this context, we have developed a facile, microwave-based procedure for the reliable and reproducible synthesis of Cu@ZnO core@shell nanowires. A systematic assessment of the effect of rationally varying various reaction conditions on this protocol was completed in order to better evaluate the growth process of these core–shell motifs. We determined that among different reaction parameters, it was the critical role of reaction time which enabled the quantitatively reliable growth of external shells with tunable thicknesses of up to 20 nm. As a demonstration of the material’s practical viability, catalytic testing was subsequently performed for the reverse water–gas shift reaction (CO 2 + H 2 → CO + H 2 O), with the evolution of the process followed with in situ X-ray diffraction and X-ray absorption spectroscopy in order to probe structural changes and gauge stability. These tests found the catalysts to be effective at converting CO 2 to CO, with notable stability detected in the shell layer and no observed alloying between copper and zinc. Our studies support the idea that the Cu–ZnO and CuO x –ZnO interfaces are essential for the effective activation of CO 2 and H 2 .

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2026-06-25
DOI
https://doi.org/10.1021/acs.jpcc.6c01300
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis and Evaluation of Cu@ZnO Core@Shell Nanowires for Use in the Carbon Dioxide Thermal Reduction Reaction

Michael G. Gallagher, Guangwen Zhou, Stanislaus S. Wong, Irene Barba-Nieto et al.
The Journal of Physical Chemistry C
Catalysts for Methane Reforming
article

Synthesis and Evaluation of Cu@ZnO Core@Shell Nanowires for Use in the Carbon Dioxide Thermal Reduction Reaction

Michael G. Gallagher, Guangwen Zhou, Stanislaus S. Wong, Irene Barba-Nieto, Kasala Prabhakar Reddy, Dali Yang, D. Michael Carnahan, Xiaobo Chen, Yuxi Wang, José A. Rodríguez, LY Zou, Edward E. Ávila, Joshua M. Garcia
article en

Abstract

Copper-based core@shell nanomaterials are of interest for the catalytic hydrogenation of carbon dioxide toward value-added products. In this context, we have developed a facile, microwave-based procedure for the reliable and reproducible synthesis of Cu@ZnO core@shell nanowires. A systematic assessment of the effect of rationally varying various reaction conditions on this protocol was completed in order to better evaluate the growth process of these core–shell motifs. We determined that among different reaction parameters, it was the critical role of reaction time which enabled the quantitatively reliable growth of external shells with tunable thicknesses of up to 20 nm. As a demonstration of the material’s practical viability, catalytic testing was subsequently performed for the reverse water–gas shift reaction (CO 2 + H 2 → CO + H 2 O), with the evolution of the process followed with in situ X-ray diffraction and X-ray absorption spectroscopy in order to probe structural changes and gauge stability. These tests found the catalysts to be effective at converting CO 2 to CO, with notable stability detected in the shell layer and no observed alloying between copper and zinc. Our studies support the idea that the Cu–ZnO and CuO x –ZnO interfaces are essential for the effective activation of CO 2 and H 2 .

The Journal of Physical Chemistry C
Binghamton University (US), State University of New York (US), Brookhaven National Laboratory (US), Universidad Yachay Tech (EC), Building Research Institute (JP), Stanford Synchrotron Radiation Lightsource (US), Division of Materials Science and Engineering (AU), National Synchrotron Light Source II, Stony Brook University (US)
Stony Brook University, Division of Chemistry, Basic Energy Sciences
Openalex Percentile: Top 19%
Catalysts for Methane Reforming
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