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The rational design of bifunctional photocatalysts with high adsorption and enrichment characteristics and excellent photocatalytic redox activity is an effective way to address environmental pollution and energy shortage crisis. In this study, cyclophosphazene‐derived porous organic polymer (PCPD) microspheres with P─N linkage are coated with graphene oxide (GO) and loaded with Ag0 nanoparticles (NPs) to prepare covalently bonded xAg‐rGO/PCPD composites. The catalyst with the highest specific surface area (denoted as 2.5Ag‐rGO/PCPD) shows excellent adsorption capacity for fluoroquinolone antibiotics, removing 96.2% of ciprofloxacin (CIP) through adsorption. By applying the catalyst with the best photocatalytic redox activity (denoted as 5Ag‐rGO/PCPD), 82.97% of refractory sulfonamide antibiotics are removed through adsorption‐degradation, and 635.3 µmol g−1 of CO and 162.3 µmol g−1 of CH4 are generated as products of CO2 photoreduction alone. Among the co‐catalytic systems, the highest CO yield of 9.16 µmol g−1 is obtained by coupling CO2 reduction with levofloxacin (LVX) degradation to harness the electron‐donating power of the pollutant molecule. This study is expected to provide useful guidance for the rational design of bifunctional photocatalysts. [ABSTRACT FROM AUTHOR]

Constructing a novel photocatalyst to realize both pollutant oxidation and evolved CO2 reduction in one photoredox cycle can significantly reframe the role of pollutant management. Here, self‐floating poly(bismaleimide‐co‐divinylbenzene) porous microspheres (PBMs) are filled with ZnSnO3 quantum dots (ZSO QDs) to construct a polymer composite microreactor with an S‐scheme heterojunction (ZSO QDs/AP‐PBMs). This microreactor realizes efficient catalytic oxidation and degradation of antibiotic pollutants under light, and the CO2 generated in this process is reduced to high value‐added CO, allowing for the direct conversion of pollutants to a resource in one photoredox cycle. The high specific surface area of the PBMs enables the rapid and efficient adsorption of levofloxacin (LVX), and the self‐floating porous design effectively solves the problem of CO2 adsorption and mass transfer in the gas–liquid–solid three‐phase system, while the S‐scheme heterostructure enhances charge carrier separation. As a result, ZSO QDs/AP‐PBMs achieves complete degradation of LVX in one redox cycle with 100% selectivity to produce 100.3 µmol g−1 CO, and further draw a conclusion that fluoroquinones antibiotics as excellent electron donors can significantly enhance co‐catalytic effect with CO2, which is not previously reported. Theoretical calculations and characterization experiments provide information on S‐scheme heterojunction transfer mechanism and possible degradation pathways, allowing for the rational design of photoredox bifunctional catalysts. [ABSTRACT FROM AUTHOR]