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With the exceptional advantages of safety, greenness, and low cost, photocatalytic H2O2 generation has kindled a wonderful spark, although being severely hampered by the terrible photoinduced exciton recombination, migration, and surface decomposition. Here, employing reflux method, the Cd–Mo–Se quantum dots of varying molar ratios of Cd and Mo were synthesized using thioglycolic acid as the capping ligand to regulate their growth. This type of metal alloying promotes rapid charge migration, improves light harvesting, and reduces the rate of charge recombination. The improved optoelectronic properties and boosted activity of Cd-rich ternary CMSe-1 QDs led to the observed exceptional photocatalytic H2O2 yield of 1403.5 μmol g−1 h−1 (solar to chemical conversion efficiency, 0.27%) under visible light, outperforming the other ternary and Se-based QD photocatalysts. Additionally, CMSe-1 shows 93.6% (2 h) hazardous Cr(VI) photoreduction. The enhanced catalytic performance of CMSe-1 corresponds to effective charge carrier separation and transfer efficiency, well supported by PL, TRPL, and electrochemical measurements. Photocatalytic H2O2 production was also studied under varying experimental conditions and the scavenger test suggests a superoxide radical intermediate 2-step single electron reduction pathway. The catalyst-assisted Cr(VI) reduction is substantiated by the zero-order kinetics as well as the determination of the pHPZC value. The catalyst can be employed for a maximum of four times while retaining its activity, according to the photostability and reusability test outcomes. This research presents interesting approaches for producing ternary QDs and modified systems for efficient photocatalytic H2O2 production and Cr(VI) reduction. [ABSTRACT FROM AUTHOR]

Graphical abstract Synergistic interaction of one dimensional CNTs with cubic spinel ZFO towards degradation of Norfloxacin and reduction of Chromium under open sun light. Abstract Development of highly efficient robust catalyst for pollutant abetment still remains an ongoing scientific challenge in the field of visible light driven photocatalysis. In this work a series of ZnFe 2 O 4 (ZFO)/carbon derivatives (ZFO@CNT, ZFO@GO, ZFO@Fullerene) nanocomposite were fabricated by one-pot hydrothermal method followed by calcination. The detail anatomical featured such as crystal geometry, morphology, elemental composition, light absorption performance, electron-hole recombination properties and photocurrent density were characterized by XRD, SEM, HRTEM, XPS, UV–Vis DRS, PL and electrochemical analysis respectively. The photocatalytic performances of ZFO@carbon nanocomposites were studied for the degradation of antibiotics (Norfloxacin) and hexavalent Chromium under open sun light illumination and the obtained results suggested that loading of carbon derivatives of ZFO nanoparticles enhance the visible light absorption capacity and excitation separation efficiency. Among the fabricated composites, ZFO@CNT exhibits the highest activity in comparison to other nanocomposites. The highest activity of ZFO@CNT is due to low photoexcited electron-hole recombination and high charge transfer properties of ZFO@CNT as confirmed via PL and impedance measurement. Further, the fabricated ZFO@CNT nanocomposite exhibited highest photocurrent density i.e. 2.25 mA/cm2 which was 225 times higher than that of neat ZFO. The optimal photocatalytic efficiency was shown by ZFO@CNT i.e. 91.36% degradation of 50 ppm norfloxacin and 82% reduction of 10 ppm Cr (VI) in 90 min and 60 min respectively under solar light irradiation. [ABSTRACT FROM AUTHOR]