Shifting syngas (an H₂/CO mixture) production away from fossil‐fuel‐dependent processes (e.g., steam methane reforming and coal gasification) is mandatory, as syngas is of interest as both a fuel and as a value‐added chemical precursor. With appropriate electrocatalysts, such as silver‐based and metal–nitrogen–carbon (M‐N‐C) materials, the electrochemical CO₂ reduction reaction (CO₂RR) allows for the production of CO alongside H₂ (from the hydrogen evolution reaction), and thus leads to syngas generation. In this Minireview, the application of M‐N‐C electrocatalysts for syngas generation is discussed. The mechanisms leading to different faradaic selectivities for CO are reviewed as a function of the nature of the metal, by using both computational and experimental approaches. The role played by the metal‐free moieties in the M‐N‐C electrocatalysts is underlined. Since M‐N‐C electrocatalysts only recently entered the CO₂RR field (as opposed to Cu‐, Ag‐, or Au‐based nanostructures), they have been mainly characterized in static liquid environments, in which the reaction rate is significantly hampered by CO₂‐dissolution/diffusion limitations. Therefore, the design of CO₂RR electrolyzers for M‐N‐C electrocatalysts is addressed, and designs such as zero‐gap electrolyzers with anionic membranes and humidified CO₂ gas feed at the cathode are highlighted.