Reaction Kinetics of Photoelectrochemical CO2 Reduction on a CuBi2O4-Based Photocathode

The CO2 reduction reaction (CO2RR) is an essential step in natural photosynthesis and artificial photosynthesis to provide carbohydrate foods and hydrocarbon energy in the carbon-neutral cycle. However, the current solar conversion efficiencies and/or product selectivity of the CO2RR are very sluggish due to its complicated multiple-step charge transfer reactions. Here, we systematically investigate the charge transfer reaction rate during CO2 reduction on CuBi2O4 photocathodes, where the surface is modified with 3-aminopropyltriethoxysilane (APTES). We discover that the surface amine group increases the charge separation rate, significantly enhancing the surface charge transfer reaction rate. However, the surface acidity has less influence on the first-order reaction, indicating that a rate-determining step (RDS) exists in the early stage of the photoelectrochemical cell (PEC) processes. Moreover, the intensity-modulated photocurrent spectroscopy (IMPS) confirms that both surface charge transfer and the recombination rate on APTES-coated CuBi2O4 are larger than bare CuBi2O4 while possessing comparable charge transfer efficiencies. Overall, the surface charge transfer reactions under the PEC condition require designing more effective nanostructured photoelectrodes and powerful characterization methods to intrinsically increase the charge separation and transfer rate while reducing the recombination rate.