Abstract
The imperative to address CO(2) emissions has prompted the search for alternative approaches to capture this gas with minimal energy consumption. In this context, leveraging the CO(2) reduction reaction (CO(2)RR) as an oxidant in fuel cells has emerged as a sophisticated strategy to convert this gas into usable energy. This study introduces a hybrid microfluidic photo fuel cell (μPFC) designed for the efficient conversion of CO(2) and glycerol into electrical energy. The prototype integrates 3D-printed components with glass sealing, enabling precise control over the reactant flow and the use of light-sensitive catalysts. The anodic glycerol electrooxidation was investigated on Pt/C dispersed on carbon paper (CP), while the CO(2)RR was carried out on CuBiO(4)/CP and CuBiO(4)/CuO/CP in the presence of solar light. Half-cell measurements demonstrate the photoactivity of CuBiO(4)/CuO/CP and CuBiO(4)/CP electrodes for the CO(2)RR under light exposure at low onset potential in a neutral pH solution, generating a positive theoretical open-circuit voltage of 0.89-0.91 V when coupled to glycerol electrooxidation in an alkaline medium. The use of the mixed medium in the membraneless system equipped with the photosensitive catalysts allowed the building of this galvanic cell. However, the feasibility of using CuBiO(4)/CP is hindered by the disruption of the colaminar channel caused by hydrogen bubbles produced during concurrent water splitting. In contrast, the μPFC equipped with a CuBiO(4)/CuO/CP photocathode demonstrates a stable and reproducible performance, delivering a maximum power density of 0.9 mW cm(-2). The formation of the CuBiO(4)/CuO heterojunction effectively suppresses photocatalytic water splitting, allowing for efficient CO(2) conversion without disruption of the laminar flow channel. This innovative approach highlights the potential of μPFCs as sustainable energy converters for the utilization of CO(2) in aqueous solutions, offering a pathway toward carbon-neutral energy production.