Enhanced selective photocatalytic reduction and oxidation of perfluorooctanoic acid on Bi/Bi5O7I decorated with poly (triazine imide)
Perfluorooctanoic acid (PFOA) is detected widely in surface and groundwater globally. Its removal poses a significant challenge due to its high chemical stability. This study demonstrates efficient PFOA degradation using poly-triazine-imides-tailored defective Bi 5 O 7 I (PTI/BB). Under 300 W Xe irradiation, 1 µg·L −1 PFOA could be degraded to 9.86 ng·L −1 after 3 h in the presence of 0.5 g·L −1 25 % PTI/BB. The mechanism investigation reveals that the oxygen vacancy (OV) in partially reduced Bi/Bi 5 O 7 I (BB) generates impurity states, enhancing the light-harvesting capacity. Furthermore, forming a type Ⅱ heterojunction between conjugated PTI and BB facilitates the efficient separation of photogenerated carriers. The resulting photogenerated electrons (reduction) and holes (oxidation) drive hydrogenation reduction and oxidative decarboxylation of PFOA, respectively. This synergistic effect consequently achieves significant defluorination of PFOA. The proposed PFOA degradation pathway via the PTI/BB catalyst offers new insights into the catalyst design for photocatalytic degradation of per- and polyfluoroalkyl substances (PFAS).
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