Abstract
We report a synthesis method for highly monodisperse Cu-Pt alloy nanoparticles. Small and large Cu-Pt particles with a Cu/Pt ratio of 1:1 can be obtained through colloidal synthesis at 300 °C. The fresh particles have a Pt-rich surface and a Cu-rich core and can be converted into an intermetallic phase after annealing at 800 °C under H2. First, we demonstrated the stability of fresh particles under redox conditions at 400 °C, as the Pt-rich surface prevents substantial oxidation of Cu. Then, a combination of in situ scanning transmission electron microscopy, in situ X-ray absorption spectroscopy, and CO oxidation measurements of the intermetallic CuPt phase before and after redox treatments at 800 °C showed promising activity and stability for CO oxidation. Full oxidation of Cu was prevented after exposure to O2 at 800 °C. The activity and structure of the particles were only slightly changed after exposure to O2 at 800 °C and were recovered after re-reduction at 800 °C. Additionally, the intermetallic CuPt phase showed enhanced catalytic properties compared to the fresh particles with a Pt-rich surface or pure Pt particles of the same size. Thus, the incorporation of Pt with Cu does not lead to a rapid deactivation and degradation of the material, as seen with other bimetallic systems. This work provides a synthesis route to control the design of Cu-Pt nanostructures and underlines the promising properties of these alloys (intermetallic and non-intermetallic) for heterogeneous catalysis.
Original language | English |
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Pages (from-to) | 5410-5421 |
Number of pages | 12 |
Journal | Journal of the American Chemical Society |
Volume | 145 |
Issue number | 9 |
DOIs | |
State | Published - Mar 8 2023 |
Externally published | Yes |
Funding
This work was primarily supported as part of the Integrated Mesoscale Architectures for Sustainable Catalysis (IMASC), an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award #DE-SC0012573. This work was carried out in part at the Singh Center for Nanotechnology, which is supported by the NSF National Nanotechnology Coordinated Infrastructure Program under grant NNCI-2025608. Additional support to the Nanoscale Characterization Facility at the Singh Center has been provided by the Laboratory for Research on the Structure of Matter (MRSEC) supported by the National Science Foundation (DMR-1720530). The Swiss Light Source at Paul Scherrer Institute, Villigen, Switzerland, is acknowledged for beamline time at the microXAS beamline (X05LA). The authors appreciate useful discussions with Drs. O. Safonova and M. Nachtegaal.
Funders | Funder number |
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Laboratory for Research on the Structure of Matter | |
Swiss Light Source at Paul Scherrer Institute | X05LA |
National Science Foundation | DMR-1720530, NNCI-2025608 |
National Science Foundation | |
U.S. Department of Energy | |
Office of Science | |
Basic Energy Sciences | -SC0012573 |
Basic Energy Sciences | |
Materials Research Science and Engineering Center, Harvard University |