Dynamic Evolution from Single-Atom Catalysts to Active Nanograins for CO<sub>2</sub> Reduction

Understanding dynamic catalyst evolution, particularly Cu-based single-atom catalysts, faces tremendous challenges of tracking rapid and nanoscale evolution and uncontrolled catalyst reoxidation during post-reaction air exposure. Although <i>ex situ</i>/<i>in situ</i> studies have indirectly indicated the structural reconstruction of single-atom catalysts, direct probing of single-atom catalyst evolution requires time-resolved nanoscale <i>operando</i> methods. Here, we present direct experimental evidence of dynamic evolution from single-atom catalysts to Cu nanostructures rich in active nanograins, based on a conductive metal-organic framework-based Cu single-atom catalyst (Cu-SAC). <i>Operando</i> synchrotron-based high-energy-resolution X-ray spectroscopy and IR absorption spectroscopy quantitatively tracked the structural and molecular fingerprints during single-atom-to-nanograin evolution. Cu-SAC supported on nanocarbon (Cu-SAC-NC) with nearly 100% metallic Cu nanograins achieved a 5-fold increase in multicarbon Faradaic efficiency (C<sub>2+</sub> FE), relative to the Cu-SAC control group with less than half metallic Cu nanograins. Cu-SAC-NC, with superior electronic conductivity provided by the nanocarbon, facilitated the formation of dense copper carbonyl (Cu-CO) intermediates, leading to a larger fraction of active metallic Cu nanograins for effective C-C coupling and significantly enhanced C<sub>2+</sub> selectivity. <i>Operando</i> electrochemical liquid-cell scanning transmission electron microscopy (EC-STEM) directly captured real-time movies of dynamic structure evolution from isolated Cu single atoms to metallic Cu nanograins under the CO<sub>2</sub>RR. <i>Operando</i> electrochemical four-dimensional (4D) STEM reveals the complex polycrystalline Cu nanostructures rich in metallic nanograin boundaries, serving as catalytically active sites. This study paves the way for the design of a new generation of single-atom catalysts based on their <i>operando</i> active structures instead of pristine structures.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-10-03
DOI
https://doi.org/10.1021/jacs.5c14123
Citations
6
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
Field-Weighted Citation Impact
2.18
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article

Dynamic Evolution from Single-Atom Catalysts to Active Nanograins for CO2 Reduction

Phillip J. Milner, Yao Yang, Bayu I. Z. Ahmad, Sungin Kim et al.
6 citations
Journal of the American Chemical Society
CO2 Reduction Techniques and Catalysts
2.18
article

Dynamic Evolution from Single-Atom Catalysts to Active Nanograins for CO2 Reduction

Phillip J. Milner, Yao Yang, Bayu I. Z. Ahmad, Sungin Kim, Ji Yong Choi, Christopher John Pollock, Yun Jeong Hwang, Shikai Liu, Juhyung Choi, Kathryn Bairley, Kwanghwi Je, Jiahong Jiang, Erik H. Thiede, Shaojinlin Yang, Sejin Park, Jihye Park, Rafael Guzman-Soriano
article en
6 citations

Abstract

Understanding dynamic catalyst evolution, particularly Cu-based single-atom catalysts, faces tremendous challenges of tracking rapid and nanoscale evolution and uncontrolled catalyst reoxidation during post-reaction air exposure. Although <i>ex situ</i>/<i>in situ</i> studies have indirectly indicated the structural reconstruction of single-atom catalysts, direct probing of single-atom catalyst evolution requires time-resolved nanoscale <i>operando</i> methods. Here, we present direct experimental evidence of dynamic evolution from single-atom catalysts to Cu nanostructures rich in active nanograins, based on a conductive metal-organic framework-based Cu single-atom catalyst (Cu-SAC). <i>Operando</i> synchrotron-based high-energy-resolution X-ray spectroscopy and IR absorption spectroscopy quantitatively tracked the structural and molecular fingerprints during single-atom-to-nanograin evolution. Cu-SAC supported on nanocarbon (Cu-SAC-NC) with nearly 100% metallic Cu nanograins achieved a 5-fold increase in multicarbon Faradaic efficiency (C<sub>2+</sub> FE), relative to the Cu-SAC control group with less than half metallic Cu nanograins. Cu-SAC-NC, with superior electronic conductivity provided by the nanocarbon, facilitated the formation of dense copper carbonyl (Cu-CO) intermediates, leading to a larger fraction of active metallic Cu nanograins for effective C-C coupling and significantly enhanced C<sub>2+</sub> selectivity. <i>Operando</i> electrochemical liquid-cell scanning transmission electron microscopy (EC-STEM) directly captured real-time movies of dynamic structure evolution from isolated Cu single atoms to metallic Cu nanograins under the CO<sub>2</sub>RR. <i>Operando</i> electrochemical four-dimensional (4D) STEM reveals the complex polycrystalline Cu nanostructures rich in metallic nanograin boundaries, serving as catalytically active sites. This study paves the way for the design of a new generation of single-atom catalysts based on their <i>operando</i> active structures instead of pristine structures.

Journal of the American Chemical SocietyVol. 147(41)
Seoul National University (KR), University of Colorado Boulder (US), Cornell University (US), University of Colorado System (US), Stanford Synchrotron Radiation Lightsource (US), Baker Engineering (United States) (US), Division of Materials Science and Engineering (AU), Institute of Natural Science (KP), Cornell High Energy Synchrotron Source
Openalex Percentile: Top 12%
CO2 Reduction Techniques and Catalysts
2.18
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