Selective Catalytic Electro-Oxidation of Water with Cobalt Oxide in Ion Impermeable Reduced Graphene Oxide Porous Electrodes
Gabriele Capilli, Yiwen Chen, Thomas Szkopek, Marta Cerruti
Abstract
The direct electrolysis of seawater is greatly inhibited by the oxidation of Cl– to free chlorine, an undesirable, corrosive byproduct. To suppress the parasitic interference of Cl– and any other ion, we developed a freestanding, electrically conducting, 3D macroporous reduced graphene oxide (rGO) scaffold with cobalt oxide particles selectively deposited on the internal walls of its closed pores (with an average diameter of ∼180 μm). The pore walls act as membranes composed of stacked rGO flakes; the nanochannels between rGO layers (size <1 nm) are permeable to water and gases while preventing the diffusion of dissolved ions such as Cl–. Due to this, the catalytic particles are selectively accessible to water molecules but not to ions, allowing electrolysis to occur without chlorine evolution. The electrodes developed exhibit a stable generation of O2 from simulated seawater at pH 14, reaching a specific current density of up to 25 A g–1 during continuous electrolysis with 89–98% Faradaic efficiency, while chlorine generation is below 6 ppm h–1, the sensitivity limit of the detection method employed. The strategy here proposed can be generalized to build electrodes that are inherently selective thanks to their architecture, with catalytically active particles loaded into closed pores with selective ion transport properties.