Kitchen-waste-derived biochar modified nanocomposites with improved photocatalytic performances for degrading organic contaminants.

Kitchen-waste-derived biochar (KBC) was produced by thermal treatment at 400 °C, and a series of KBC/BiOX (X = Br, Cl) photocatalysts were developed using ultrasonication and solvothermal treatment. The as-prepared photocatalysts were characterized by several tests and investigated by photocatalytic reactions towards methyl orange (MO) and tetracycline (TC). The best photocatalysts, 0.15KBC/BiOBr and 0.15KBC/BiOCl separately achieved complete MO photodegradation in 20 min and 35 min. Further study confirmed that 0.15KBC/BiOBr and 0.15KBC/BiOCl possessed excellent photocatalytic efficiency that was 17.9 and 14.8 times higher than BiOBr and BiOCl, respectively. In addition, 0.15KBC/BiOX showed higher activity removal of TC than pure BiOX in 60 min. Notably, 0.15KBC/BiOX maintained a reproducible high photocatalytic efficiency after five recycles. Estimated band gap energy for 0.15KBC/BiOBr (2.40 eV) and 0.15KBC/BiOCl (3.00 eV) was considerably lower than that of BiOBr (2.73 eV) and BiOCl (3.30 eV), indicating a delocalized state was created when forming electronic pathways on the interface. Besides, visible-light harvesting of photocatalysts got promoted by the modification of KBC. Active species trapping experiments and electron paramagnetic resonance (EPR) tests illustrated that photogenerated holes were the principal active species, while ∙OH was involved in the reaction. The successful synthesis of 0.15KBC/BiOX catalyst provided a new approach on simultaneously degrading organic contaminants in water and disposing of excessive kitchen waste.

In situ preparation of visible-light-driven carbon quantum dots/NaBiO3 hybrid materials for the photoreduction of Cr(VI).

In this study, different carbon quantum dots (CQDs)/NaBiO3 hybrid materials were synthesized as photocatalysts to effectively utilize visible light for the photocatalytic degradation of contaminants effectively. These hybrid materials exhibit an enhanced photocatalytic reduction of hexavalent chromium (Cr(VI)) in the aqueous medium. Zero-dimensional nanoparticles of CQDs were embedded within the two-dimensional NaBiO3 nanosheets by the hydrothermal process. Compared with that of the pure NaBiO3 nanosheets, the photocatalytic performance of the hybrid catalysts was significantly high and 6 wt.% CQDs/NaBiO3 catalyst exhibited better photocatalytic performance. We performed the first-principles density functional theory calculations to study the interfacial properties of pure NaBiO3 nanosheets and hybrid photocatalysts, and confirmed the CQDs played an important role in the CQDs/NaBiO3 composites. The experimental results indicated that the enhanced reduction of Cr(VI) was probably due to the high loading of CQDs (electron acceptor) on NaBiO3, which made NaBiO3 nanomaterials to respond in visible light and significantly improved their electron-hole separation efficiency.

Visible-light-driven simultaneous decontamination of multi-antibiotics by facile synthesized BiOCl loaded food wastes biochar.

Environmental dissemination caused by widespread use of antibiotics has been regarded as a possible hazard to aquatic ecosystem and human health. The increasing misgivings make it imperative to develop a novel catalyst with remarkable visible-light-driven activity to remove antibiotics, especially for their simultaneous decontamination. Herein, C/BiOCl composites were successfully prepared by decorating BiOCl nanosheets on food wastes biochar (C) by a simple hydrolysis strategy. Not only the binary system of tetracycline antibiotics, but also the ternary mixture could be simultaneously photodegraded over 25% C/BiOCl within 15 min irradiation. The improved photocatalytic activities could be ascribed to the introduction of biochar, endowing increased surface area, enhanced separation of photo-generated charge carriers, and better light absorption. The as-prepared 25% C/BiOCl also demonstrated satisfactory stability and positive removal effect in actual water samples. The present work provides new insights into the development of biochar-based photocatalysts for simultaneous degradation of multiple antibiotics.

Improving photocatalytic activity under visible light over a novel food wastes biochar-based BiOBr nanocomposite.

Biochar (C) applied in synthesizing photocatalysts to eliminate water pollution has been intensively investigated. Herein we report the first use of biochar pyrolyzed from food wastes at 400 °C (400C) and 700 °C to construct C/BiOBr composites via a facile hydrolysis approach. Photocatalytic performances could be significantly improved by choosing the appropriate carbonization temperature and adjusting the content of C in C/BiOBr composites. The prepared 1%400C/BiOBr exhibited the best photodegradation capacity towards methylene orange (20 mg/L) and tetracycline (50 mg/L). A series of characterization results illustrated that smooth structure and surface properties (oxygen functional groups and persistent free radicals) of 400C played an important role in enhancing the photocatalytic activities. Mechanism exploration suggested that h+ and ˙O2- were the main active species thus contributing to photodegradation. This study provided a new insight into utilization of biochar derived from food wastes in photocatalysis and environmental remediation.

Facile construction of 2D g-C3N4 supported nanoflower-like NaBiO3 with direct Z-scheme heterojunctions and insight into its photocatalytic degradation of tetracycline.

Photocatalytic oxidation using solar energy is a promising green technology to degrade antibiotic contaminants. Herein, a 2D g-C3N4 supported nanoflower-like NaBiO3 with direct Z-scheme heterojunction was synthesized via a facile hydrothermal approach, and the photocatalytic performance of g-C3N4/NaBiO3 was remarkable better than that of g-C3N4 and NaBiO3 for tetracycline degradation under visible light. Photoinduced electrons accumulated on the conduction band of g-C3N4 and holes gathered on the valence band of NaBiO3, which was more suitable for generating superoxide and hydroxyl radicals. Meanwhile, the built-in electric field between g-C3N4 and NaBiO3 was proved by their different work functions based on DFT calculations, which enhanced the charges separation. The formed radicals were determined by ESR, and their role in the degradation of tetracycline was examined by the active species trapping test. Moreover, the sites attacked by free radicals and degradation pathways for tetracycline were inferred by the results of Gaussian 09 program and HPLC-MS. The effects of water matrix and three other organic contaminants was further studied for actual use evaluation. Importantly, the prepared g-C3N4/NaBiO3 showed stable photodegradation activity for eight cycles. This work not only provides a promising photocatalyst, but also gets insight into the photocatalytic removal of tetracycline.

A Promising Alternative for Sustainable and Highly Efficient Solar-Driven Deuterium Evolution at Room Temperature by Photocatalytic D2 O Splitting.

Motivated by energy shortages and in view of current efforts to develop clean, renewable energy sources based on fusion, a solar-driven strategy has been developed for deuterium evolution. Deuterium is a critical resource for many aspects. However, the limited natural abundance of deuterium and the complexity of established technologies, such as quantum sieving (QS) for deuterium production under extreme conditions, pose challenges. The new method has the potential for robust and sustainable deuterium evolution, enabling deuterium production at a high rate of 9.745 mmol g-1 h-1 . The activity, thermodynamic, and kinetic characteristics are also investigated and compared between photocatalytic heavy water (D2 O) splitting and water (H2 O) splitting. This study opens a new avenue to discover promising photocatalytic deuterium generation systems for advanced solar energy utilization and deuterium enrichment.