Rito Yanagi1,Tianshuo Zhao2,Matthew Cheng1,Daniel King3,Zhaohan Li1,Shu Hu1
Yale University1,University of Pennsylvania2,Texas A&M University3
Rito Yanagi1,Tianshuo Zhao2,Matthew Cheng1,Daniel King3,Zhaohan Li1,Shu Hu1
Yale University1,University of Pennsylvania2,Texas A&M University3
Photocatalytic CO<sub>2</sub> reduction (CO<sub>2</sub>R) promises scalable conversion of atmospheric CO<sub>2</sub> to chemicals or fuels. Currently, most photocatalytic CO<sub>2</sub>R systems require concentrated and gaseous CO<sub>2</sub> as feedstock. This process requires extra energy and carbon footprint, especially when separating 410 ppm CO<sub>2</sub> directly from the air. We demonstrate a design that enables photocatalytic CO<sub>2</sub>R and local CO<sub>2</sub> production simultaneously using photocatalytic panels consist of III-V semiconductors and reversible quinone redox mediators. Our design, which draws inspiration from photosynthesis, consists of enriching CO<sub>2</sub> in a (bi)carbonate solution, spatially separating surface reaction sites and driving local pH swing to release CO<sub>2</sub> locally, and reducing CO<sub>2</sub> into CO<sub>2</sub>R products eventually. We show that in the presence of quinone redox couples in a bicarbonate solution, CO is produced in a 1-atm Ar environment where the only source of CO<sub>2</sub> is the (bi)carbonate anions. Finally, we construct a COMSOL Multiphysics model that accounts for all the reaction kinetics to simulate the photocatalytic reaction during operation