Quantification of the porosity in template-based ordered porous Ag electrodes and its effect on electrochemical CO₂...

The electrochemical reduction of CO₂ combined with efficient CO₂ capture is a promising approach to close the carbon cycle. We studied the effect of pore size on the activity and selectivity of porous Ag electrodes using template-based electrodes as model catalysts. Using polymer spheres with sizes between 115 nm and 372 nm as templates, ordered porous Ag catalysts with different pore diameters were obtained. These well-defined model systems allowed us to understand the effect of pore size on CO and H₂ production. At the most cathodic potential, around -1.05 V, up to 4 times more CO than H₂ was formed. The intrinsic CO production depends on the pore size, as it increases when changing the pore diameters from ∼100 nm to ∼300 nm. At pore diameters above ∼300 nm, the pore size does not affect the intrinsic CO production anymore. For the first time, FIB-SEM was used to quantitatively analyse the porosity of the electrodes and correlate it with trends in intrinsic activity. The catalyst with a pore diameter of ∼200 nm had the highest tortuosity of 2.41, which led to an increased CO production. The catalysts with a pore diameter of ∼200 nm and smaller have pore networks that are twice as long as the pore network of catalysts with ∼400 nm pores. This leads to an additional potential drop, which lowers the effective driving force for the electrochemical reaction. Disentanglement of these different factors is important for rational design of porous CO₂ reduction catalysts.