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High selectivity and fast charge separation are two important factors for photocatalytic wastewater treatment. Herein, we prepared a molecular imprinted Ag/Ag 3 VO 4 /g-C 3 N 4 photocatalyst (MIP) that exhibited great specific recognition ability along with excellent photocatalytic activity. The ultrathin g-C 3 N 4 nanosheets with high surface are used to prepare. The Z-scheme Ag 3 VO 4 /g-C 3 N 4 heterostructure and the surface plasmon resonance of the photoreduced Ag0 together contributed to the improvement of the separation efficiency of photogenerated electrons and holes. In addition, MIP provides the specific recognition ability to preferentially adsorb the target pollutant. The selectivity of photocatalysis was evaluated by the degradation of oxytetracycline and tetracycline solutions. Photoluminescence and transient photocurrent measurements further prove the improved charge separation efficiency of MIP. A plausible photocatalytic reaction mechanism is proposed based on electron spin resonance measurement and the active species trapping experiments, where indicates that the main active species of this photocatalytic process are O 2 − and h+. This research provides an effective strategy for the simultaneous enhancement of selectivity and activity via molecular imprinting. [ABSTRACT FROM AUTHOR]

Achieving the intelligent controllability of the photocatalyst to the surrounding environment is a very meaningful work. Here, the polyacrylic acid (PAA) modified Ag/AgCl-40/CN composite was constructed to achieve an intelligent response of pH value. PAA exhibits hydrophilic properties at high pH value, increasing the adsorption capacity to tetracycline (TC) molecules. The morphology of PAA from contracted state to diastolic state, releasing the Ag/AgCl-40/CN catalyst. In addition, PAA modified Ag/AgCl-40/CN can prevent the loss of AgCl. The g-C 3 N 4 nanosheets (CN) as a carrier enhance the dispersibility of the AgCl particles. The LSPR effects of Ag nanoparticles produce more electrons acting on photocatalytic degradation. On the results of experiment, the degradation of TC by PAA@Ag/AgCl-40/CN shows an excellent degradation activity when the high pH value. Photoluminescence spectroscopy and photocurrent demonstrate that carrier separation efficiency of PAA@Ag/AgCl-40/CN is higher than CN and Ag/AgCl-40/CN. The detection of the main active substances •O 2 − and h+, revealing a reasonable mechanism for the PAA@Ag/AgCl-40/CN hybrid system. This work provides a procedure to obtain smart materials that can switch photocatalytic processes. [ABSTRACT FROM AUTHOR]