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Pulsed Potentials on Copper Tune CO2 Conversion Toward Ethanol or Ethylene

Peer-reviewed imaging ties dynamic Cu(100) surface states to controllable CO2-to-fuels selectivity under a pulsed protocol.

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CO2 and fuel cylinders.

Overview

  • The Nature Catalysis study reports that alternating anodic (~+0.6 V) and cathodic (~−1 V) pulses reshape and partially oxidize Cu(100), boosting CO2 electroreduction performance.
  • Inverted-pyramid faceting forms during oxidizing pulses via site-selective dissolution, creating specific side facets linked to product outcomes.
  • Following reduction pulses, the surface adopts a sandwich-like near-surface with ~0.5 nm metallic Cu over ~0.5 nm Cu(I), which emerges from partial reduction of an oxidized film.
  • Correlated LEEM/XPEEM spectro-microscopy directly connects these morphological and chemical-state changes to shifts in selectivity between ethanol and ethylene.
  • The Fritz Haber Institute team demonstrates tunability on single-crystal model electrodes after short pulsed CO2RR runs, with practical durability and scale-up still untested.