Electrochemical CO2 reduction is the cathodic conversion of carbon dioxide into carbon monoxide, formate, hydrocarbons or alcohols, driven by electricity at an electrode surface whose structure decides which intermediates are stabilised. Selectivity rather than activity is the central problem, because the competing hydrogen evolution reaction shares the potential window and often the active site, and catalyst design therefore has to be considered together with mass transport [1]. Reactor configuration matters as much as catalyst identity: gas-diffusion electrodes, electrolyte composition and cell geometry set the local concentration at the interface and hence which pathway dominates [2]. Bismuth, tin and indium cathodes give formate with high faradaic efficiency because their surfaces favour the adsorbed precursor over carbon monoxide [3]. Bimetallic oxides shift selectivity through interface sites rather than through either component alone [4], while molecular catalysts, metalloporphyrins among them, offer defined sites whose mechanism can be computed directly [5]. Comparing reports across cells stays difficult because local pH and transport are rarely documented together.