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.
Authors
- Phillip J. Milner (ORCID: https://orcid.org/0000-0002-2618-013X)
- Yao Yang (ORCID: https://orcid.org/0000-0003-0321-3792)
- Bayu I. Z. Ahmad
- Sungin Kim (ORCID: https://orcid.org/0000-0001-9107-0781)
- Ji Yong Choi (ORCID: https://orcid.org/0000-0001-9738-3543)
- Christopher John Pollock (ORCID: https://orcid.org/0000-0001-5736-513X)
- Yun Jeong Hwang (ORCID: https://orcid.org/0000-0002-0980-1758)
- Shikai Liu (ORCID: https://orcid.org/0000-0001-9689-3090)
- Juhyung Choi (ORCID: https://orcid.org/0000-0003-0770-6113)
- Kathryn Bairley (ORCID: https://orcid.org/0000-0003-0975-0652)
- Kwanghwi Je (ORCID: https://orcid.org/0000-0002-5017-6034)
- Jiahong Jiang
- Erik H. Thiede (ORCID: https://orcid.org/0000-0002-5666-1372)
- Shaojinlin Yang
- Sejin Park (ORCID: https://orcid.org/0000-0002-5859-4433)
- Jihye Park (ORCID: https://orcid.org/0000-0002-8644-2103)
- Rafael Guzman-Soriano
Institutions
- 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
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