LAUSR

Photocatalytic water treatment has significant potential to disinfect and degrade recalcitrant organic pollutants while minimizing the need to add chemicals, but current approaches have poor energy efficiency due, in part, to inefficient utilization of photo-generated reactive oxygen species (ROS). Organic coatings such as cyclodextrin (CD) can adsorb target contaminants and bring them close to the photocatalyst surface to enhance ROS utilization efficiency, but the coatings themselves are susceptible to ROS attack. Here, we report an ROS-resistant fluorinated CD polymer (CDP) that can both adsorb contaminants and resist degradation by ROS, yielding a more efficient material for "trap and zap" water treatment. We produced the CDP through condensation polymerization of β-cyclodextrin and tetrafluoroterephthalonitrile, resulting in a cross-linked, covalently bound CD film that is much more stable than prior approaches involving physi-sorption. We optimized the coating thickness on TiO2 microspheres to improve the efficiency of contaminant degradation, and found that increasing the CDP content enhanced BPA adsorption but also occluded photocatalytic sites and hindered photocatalytic degradation. The optimum content of CDP was 5% by weight, and this optimal CDP-TiO2 composition had a BPA adsorption capacity of 36.9 ± 1.0 mg g-1 compared with 24.1 ± 1.1 mg g-1 for CD-coated TiO2 (CD-TiO2) and 21.9 ± 1.5 mg g-1 for bare TiO2. CDP-TiO2 exhibited minimal photoactivity loss after 1000 h of repeated use in DI water under UVA irradiation (365 nm, 3.83 × 10-6 E L-1s-1), and no release of organic carbon from the coating was detected. Photocatalytic treatment using CDP-TiO2 only showed a small decrease in BPA removal efficiency in secondary effluent after four 3-h cycles, from 80.2% to 71.7%. In contrast, CD-TiO2 and P25 removed only 29.8% and 6.2% of BPA after 4 cycles, respectively. Altogether, the CDP-TiO2 microspheres represent promising materials for potential use in photocatalytic water treatment.