| So far,oxygen reduction reaction(ORR)plays a crucial role in the photocatalytic process,which can produce a large amounts of reactive oxygen species(ROS)on the premise of having enough electrons.It is well known that ROS include superoxide radicals(·O2-)and hydroxyl radicals(·OH).Both have strong oxidizability and can react with organic pollutants rapidly,efficiently degrading them into small molecules and even mineralizing them into CO2 or H2O.Due to the easy recombination of photogenerated electrons and holes,the single BiOBr material cannot provide sufficient electrons for the ORR in the system,resulting in insufficient ORR and less·O2-as well as·OH generated in the system,which affects the photocatalytic activity of the material.In order to maximize the rate of ORR,we propose to construct BiOBr-P/BiOBr-F(BPF-1/1)homojunction.The photocatalysts were systematically characterized by various analysis and testing methods,and the reaction mechanism of the system was investigated.The research progress achieved in this paper is as follows:(1)BPF-1/1 homojunction photocatalyst was prepared by in-situ synthesis.XRD,FTIR,SEM,TEM and other characterization results indicated that BPF-1/1homojunction had been constructed,which presented interlaced structure.XPS and DFT confirmed the formation of internal electric field in BPF-1/1 homojunction and the flow of electrons from BiOBr-F to BiOBr-P.(2)Taking tetracycline(TC)as the target pollutant,the photocatalytic activities of BiOBr-P,BiOBr-F,BPF-1/2,BPF-2/1,BPF-4/1 and BPF-1/1 homojunctions were evaluated.The TC degradation rate by BPF-1/1 homojunction reached 97.80%within120 min,and the experimental results proved that BPF-1/1 homojunction had the best photocatalytic activity.The control variable method was adopted to change the single experimental conditions,and it was found that the most suitable reaction conditions for the reaction were p H=7,the amount of catalyst added was 0.50 g/L,the light intensity was set to 500 W,and the initial concentration of TC was set to 0.02 g/L.Through cycling experiments and XRD characterization before and after the material reaction,the TC degradation efficiency by BPF-1/1 homojunction still reached 96.90% after four cycle experiments,which only decreased by 0.90%,and the structure of BPF-1/1homojunction did not change,suggesting that the catalyst has good recyclability and stability.(3)The BPF-1/1 homojunction could effectively shorten the channel of electron transfer and accelerate the separation of carriers as verified by EIS,transient photocurrent response and PL.Meanwhile,the quantification of·O2-,·OH and H2O2showed that BPF-1/1 homojunction could accelerate the ORR to generate more·O2-and·OH than individual materials.In addition,the GC-MS technique was used to analyze the intermediates of TC degradation process and detect the toxicity index of the intermediates,and the results demonstrated that the BPF-1/1 homojunction photocatalytic degradation of TC is not harmful to the environment.Therefore,the construction of homojunctions is conducive to more electrons participating in ORR,generating a large number of active species and accelerating the efficiency of photocatalytic degradation of TC. |