Efficient photocatalytic degradation of emerging ciprofloxacin under visible light irradiation using BiOBr/carbon quantum dot/saponite composite.

The use of visible-driven photocatalysts has fascinated attention as a capable and sustainable approach for wastewater remediation. In this work, BiOBr/carbon quantum dot (CQDs)/saponite composites (CQDs/Clay@BiOBr) were fabricated via hydrothermally using two different CQDs/Clay precursors (in-situ synthesis (IS) and physical mixing (PM)). The obtained products were characterized, and the photocatalytic performances of the prepared samples were evaluated in the photocatalytic decomposition of emerging ciprofloxacin (CIP) pharmaceutical waste. The highest CIP mineralization performance was achieved when a combination of BiOBr and CQDs/Clay (IS) with the appropriate proportion because the strong adhesion between CQDs and clay generate a great heterojunction in the composite. The stronger interaction of CQDs and better distribution of CQDs on the surface of clay in the CQDs/Clay (IS) enhanced the interaction of BiOBr and CQDs, and avoided the re-agglomeration of excess of CQDs on surface of BiOBr which reduce the active surface to receive the light and react with CIP. The ultrafast degradation rate of the optimized CQDs/Clay@BiOBr composite was better compared to others. The significant improvement in the CIP degradation efficiency of the CQDs/Clay@BiOBr composite was attributed to the excellent separation and transportation of photogenerated electrons and holes, as confirmed by photoluminescence, photocurrent density, and electrochemical impedance spectroscopy results. Moreover, the photocatalytic degradation mechanism of CIP in the CQDs/Clay@BiOBr composite was proposed based on the electronic states of each material in the composite and on a scavenger test. Thus, the proposed CQDs/Clay@BiOBr composite can be employed as a potential visible-light-driven photocatalyst for the decomposition of organic contaminants in wastewater.

One-step solvent-free synthesis of carbon dot-based layered composites exhibiting color-tunable photoluminescence.

We here report a practical and green approach to the development of luminescent composites through in situ solvent-free formation of carbon dots on layered inorganic compounds. The composites exhibit higher solid-state photoluminescence than those prepared by mixing of synthesized carbon dots and layered clay minerals. Tuning of the emission color of the composites has also been achieved by the addition of small molecules into phloroglucinol as starting materials for carbonization. The carbon dots synthesized in clay compounds in the solvent-free conditions are well-dispersed to obtain homogeneous composites. Furthermore, we have demonstrated that highly luminescent carbon dots are formed by carbonization in the presence of layered inorganic compounds. The one-step solvent-free approach presented in this work may allow not only facile, economical, and sustainable production of nanostructured carbon dot-based composites but also improvement of their luminescence properties.