RESUMO
Most photoelectrocatalytic (PEC) reactions are performed in the liquid phase for convenient electron transfer in an electrolyte solution. Herein, a novel PEC reactor involving a tandem combination of TiO2 nanorod array/fluorine-doped tin oxide (TiO2-NR/FTO) working electrodes and an electrochemical auxiliary cell was constructed to drive the highly efficient PEC oxidation of indoor gas (NOx). With the aid of a low bias voltage (0.3 V), the as-formed PEC reactor exhibited an 80% removal rate for oxidizing NO (500 ppb) under light irradiation, which is much higher than that of the traditional photocatalytic (PC) process. Upon being irradiated by light, the photogenerated electrons are quickly separated from the holes and transferred to the counter electrode (Pt) owing to the applied bias voltage, leaving photogenerated holes in the TiO2-NR/FTO electrode for oxidizing NO molecules. Moreover, both dry and humid NO could be effectively removed by the tandem TiO2-NR/FTO-based gas-phase PEC reactor, indicating that the NO molecules could also be directly oxidized by photogenerated holes in addition to hydroxyl radicals. The presence of trace amounts of water could promote the PEC oxidation of NO owing to the formation of hydroxyl radicals induced by reactions between the water and holes, which could further oxidize NO. This PEC reactor offers an energy-saving, environmentally friendly, and efficient route to treat air polluted with low concentrations of gases (NOx and SOx).