Superconformal electrodeposition is explained based on a local growth veloc
ity that increases with coverage of a catalytic species adsorbed on the cop
per-electrolyte interface. For dilute concentration of the catalyst precurs
or in the electrolyte, local coverage in fine features changes more due to
interface area change than by accumulation from the electrolyte, yielding s
uperconformal growth. The model is supported by experiments and simulations
of copper deposition in 350-100 nm wide features, helping to explain the i
nfluence of adsorbates on roughness evolution.