4.8 Article

Tuning Sn-Catalysis for Electrochemical Reduction of CO2 to CO via the Core/Shell Cu/SnO2 Structure

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 12, Pages 4290-4293

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b00261

Keywords

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Funding

  1. U.S. Army Research Laboratory
  2. U.S. Army Research Office under the Multi University Research Initiative (MURI) [W911NF-11-1-0353]
  3. National 1000 Young Talents Program of China
  4. National Natural Science Foundation of China [21603078]
  5. National Materials Genome Project [2016YFB0700600]

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Tin (Sn) is known to be a good catalyst for electrochemical reduction of CO2 to formate in 0.5 M KHCO3. But when a thin layer of SnO2 is coated over Cu nanoparticles, the reduction becomes Sn-thickness dependent: the thicker (1.8 nm) shell shows Sn-like activity to generate formate whereas the thinner (0.8 nm) shell is selective to the formation of CO with the conversion Faradaic efficiency (FE) reaching 93% at 0.7 V (vs reversible hydrogen electrode (RHE)). Theoretical calculations suggest that the 0.8 nm SnO2 shell likely alloys with trace of Cu, causing the SnO2 lattice to be uniaxially compressed and favors the production of CO over formate. The report demonstrates a new strategy to tune NP catalyst selectivity for the electrochemical reduction of CO2 via the tunable core/shell structure.

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