Electrochemical CO 2 reduction was examined on high-area transition metal catalysts supported on nanoporous activated carbon fiber (ACF) supports, in the form of gas diffusion electrodes, in aqueous KHCO 3 solution. The most active catalyst was ACF/Ni, on which up to ca 65 mA cm À2 current density for CO production was observed, with simultaneous production of hydrogen of ca 15 mA cm À2 at À1.6 V vs SCE. At more negative potentials, higher H 2 /CO ratios can be obtained. The reaction mechanism for CO production probably involves a chemical reaction between CO 2 and the radical anion CO 2 .À to produce the CO 2 dimer radical anion (CO 2 ) 2 .À . The results are compared with those for photoelectrochemical CO 2 reduction on p-InP, on which the mechanism is thought to involve the one-electron reduction of two adsorbed CO 2 molecules to produce the CO 2 dimer radical anion.In contrast to the behavior for hydrogen evolution, the PCD values for CO 2 reduction did not vary greatly with potential. However, the values varied considerably for the different catalysts. As already described, the ACF/Ni catalyst exhibited the high-