<p></p><p>Carbon dioxide electrochemical reduction (CO<sub>2</sub>ER) has attracted considerable attention as a technology to recycle CO<sub>2</sub> into raw materials for chemicals using renewable energies. We recently found that Zn-Al layered double hydroxides (Zn-Al LDH) have the CO-forming CO<sub>2</sub>ER activity. However, the activity was only evaluated by using the liquid-phase CO<sub>2</sub>ER. In this study, Ni-Al and Ni-Fe LDHs as well as Zn-Al LDH were synthesized using a facile coprecipitation process and the gas-phase CO<sub>2</sub>ER with the LDH-loaded gas-diffusion electrode (GDE) was examined. The products were characterized by XRD, STEM-EDX, BF-TEM and ATR-IR spectroscopy. In the ATR-IR results, the interaction of CO<sub>2</sub> with Zn-Al LDH showed a different carbonates evolution with respect to other LDHs, suggesting a different electrocatalytic activity. The LDH-loaded GDE was prepared by simple drop-casting of a catalyst ink onto carbon paper. For gas-phase CO<sub>2</sub>ER, only Zn-Al LDH exhibited the CO<sub>2</sub>ER activity for carbon monoxide (CO) formation. By using different potassium salt electrolytes affording neutral to strongly basic conditions, such as KCl, KHCO<sub>3</sub> and KOH, the gas-phase CO<sub>2</sub>ER with Zn-Al LDH-loaded GDE showed 1.3 to 2.1 times higher partial current density for CO formation than the liquid-phase CO<sub>2</sub>ER.</p><p></p>