Graphene-doped CuO (rGO-CuO) nanocomposites with flower shapes were prepared by an improved solvothermal method. The samples were characterized by X-ray diffraction, X-ray photoelectron spectroscopy and UV–visible spectroscopy. The active species in the degradation reaction of rGO-CuO composites under ultrasonic irradiation were detected by electron paramagnetic resonance. On the basis of comparative experiments, the photodegradation mechanisms of two typical dyes, Rhodamine B (Rh B) and methyl orange (MO), were proposed. The results demonstrated that the doped CuO could improve the degradation efficiency. The catalytic degradation efficiency of rGO-CuO (2:1) to rhodamine B (RhB) and methyl orange (MO) reached 90% and 87% respectively, which were 2.1 times and 4.4 times of the reduced graphene oxide. Through the first-principles and other theories, we give the reasons for the enhanced catalytic performance of rGO-CuO: combined with internal and external factors, rGO-CuO under ultrasound could produce more hole and active sites that could interact with the OH· in pollutant molecules to achieve degradation. The rGO-CuO nanocomposite has a simple preparation process and low price, and has a high efficiency of degrading water pollution products and no secondary pollution products. It has a low-cost and high-efficiency application prospect in water pollution industrial production and life.

Photocatalytic reduction of CO₂ is considered as a kind of promising technologies for solving the greenhouse effect. Herein, a novel hybrid structure of g-C₃N₄/ZnO/Ti₃C₂ photocatalysts was designed and fabricated to investigate their abilities for CO₂ reduction. As demonstration, heterojunction of g-C₃N₄/ZnO can improve photogenerated carriers' separation, the addition of Ti₃C₂ fragments can further facilitate the photocatalytic performance from CO₂ to CO. Hence, g-C₃N₄/ZnO/Ti₃C₂ has efficiently increased CO production by 8 and 12 times than pristine g-C₃N₄ and ZnO, respectively. Which is ascribed to the photogenerated charge migration promoted by metallic Ti₃C₂. This work provides a guideline for designing efficient hybrid catalysts on other applications in the renewable energy fields.

Aqueous zinc-ion batteries (AZIBs) are regarded as promising electrochemical energy storage devices owing to its low cost, intrinsic safety, abundant zinc reserves, and ideal specific capacity. Compared with other cathode materials, manganese dioxide with high voltage, environmental protection, and high theoretical specific capacity receives considerable attention. However, the problems of structural instability, manganese dissolution, and poor electrical conductivity make the exploration of high-performance manganese dioxide still a great challenge and impede its practical applications. Besides, zinc storage mechanisms involved are complex and somewhat controversial. To address these issues, tremendous efforts, such as surface engineering, heteroatoms doping, defect engineering, electrolyte modification, and some advanced characterization technologies, have been devoted to improving its electrochemical performance and illustrating zinc storage mechanism. In this review, we particularly focus on the classification of manganese dioxide based on crystal structures, zinc ions storage mechanisms, the existing challenges, and corresponding optimization strategies as well as structure–performance relationship. In the final section, the application perspectives of manganese oxide cathode materials in AZIBs are prospected.