Advances in nanotechnology and nanomaterials have attracted considerable interest and play key roles in scientific innovations in diverse fields. In particular, increased attention has been focused on carbon-based nanomaterials exhibiting diverse extended structures and unique properties. Among these materials, zero-dimensional structures, including fullerenes, carbon nano-onions, carbon nanodiamonds, and carbon dots, possess excellent bioaffinities and superior fluorescence properties that make these structures suitable for application to environmental and biological sensing, imaging, and therapeutics. This review provides a systematic overview of the classification and structural properties, design principles and preparation methods, and optical properties and sensing applications of zero-dimensional carbon nanomaterials. Recent interesting breakthroughs in the sensitive and selective sensing and imaging of heavy metal pollutants, hazardous substances, and bioactive molecules as well as applications in information encryption, super-resolution and photoacoustic imaging, and phototherapy and nanomedicine delivery are the main focus of this review. Finally, future challenges and prospects of these materials are highlighted and envisaged. This review presents a comprehensive basis and directions for designing, developing, and applying fascinating fluorescent sensors fabricated based on zero-dimensional carbon nanomaterials for specific requirements in numerous research fields.

Zero-Dimensional Carbon Nanomaterials for Fluorescent Sensing and Imaging.

Removal of tetracycline antibiotics by adsorption and photocatalytic-degradation processes in aqueous solutions using metal organic frameworks (MOFs): A systematic review

For improving the mechanical properties of tungsten, HfC–W composites were fabricated by ball milling and spark plasma sintering process. The microstructure and mechanical properties of the composites were investigated. The interdiffusion of the Hf and W atoms during sintering produced a mixed carbide, identified as (Hf,W)C. This interfacial mixed carbide helped in developing a good interface joint with the adjacent W matrix. The increase in mechanical properties of the HfC–W composite at room temperature as well as high temperature was attributed to the reinforcement effect of the HfC particles. One of the strengthening mechanisms of the composite can be attributed to the formation of mixed carbide (Hf,W)C by interdiffusion at the interface, which assured the effective load transfer from the W matrix to the hard HfC particles.

The effect of HfC content on mechanical properties HfC–W composites

A new tungsten matrix composite containing 30 vol% titanium carbide particles (W-TiC) produced by sintering under 20 MPa pressure at 2000°C in a vacuum has been developed in order to improve the elevated temperature strength of tungsten. Flexural strength tests of the W-TiC composite in the temperature range 20–1200°C showed that the strength was significantly increased by the presence of TiC particles. The flexural strength at 1000°C was 1155 MPa, which was much higher than that at 20°C (770 MPa). Microstructural observations showed that a interdiffusion zone was produced at the W matrix-TiC particle interface, and a strong bond was formed between TiC and W, which was very beneficial to the elevated temperature mechanical properties. The mechanisms of fracture at 20°C and 1000°C were investigated. The fracture at 20°C was brittle. There was a growth-coalescence process for the initial cracks during the fracture process of the W-TiC composite at 1000°C, and the W matrix exhibited ductile tearing. The excellent elevated temperature strength of W-TiC composite was attributed to the brittle-ductile transition in the W matrix, which allows more effective strengthening from TiC particles.

The microstructure and elevated temperature strength of tungsten-titanium carbide composite

Due to the uncontrolled synthesis of layered double hydroxides (LDHs), a simple and efficient strategy was needed to construct high-performance LDHs. Herein, Co-Mn-ZIF was used as the sacrificial template to form cobalt-manganese-nickel LDH (M−Co−Mn−Ni LDH) through the process of deconstruction and reconstruction. Due to the sufficient in-situ etching of the Co-Mn-ZIF template, M−Co−Mn−Ni LDH exhibited a larger specific surface area (482.4 m2/g) and pore volume (3.3 × 10−2 cm3/g) as well as easier diffusion and interaction with reaction sites of organic molecules. The prepared M−Co−Mn−Ni LDH showed high catalytic performance for the degradation of enrofloxacin (ENR) by activating peroxymonosulfate (PMS), with the removal rate of 88.5 % within 30 min. The quenching reaction and electron paramagnetic resonance (EPR) analysis results indicated that SO4•− and 1O2 were main active substances in the oxidation process of ENR. In addition, the Co-Mn-Ni LDH/PMS system was stable and almost unaffected by pH values, organic and inorganic substances, and it could achieve high removal efficiency in various pollutant samples. This work provided a convenient and efficient approach for the construction of high-performance MOFs derived LDHs catalysts. 

Performance and mechanism of efficient activation of peroxymonosulfate by Co-Mn-ZIF derived layered double hydroxide for the degradation of enrofloxacin

Cobalt-based catalysts for heterogeneous peroxymonosulfate (PMS) activation in degradation of organic contaminants: Recent advances and perspectives

Natural deep eutectic solvent assisted synthesis and applications of chiral carbon dots

Constructing nano-heterojunction of MOFs with crystal regrowth for efficient degradation of tetracycline under visible light

Considering the selective pharmacological activity and ecotoxicity of chiral drugs, the development of chiral materials with the dual functions of enantiomeric recognition and adsorption is of great significance. Herein, a novel bifunctional chiral composite (Fe3O4/CCDs@HP-ZIF-8) which does not contain expensive and rare fluorescent chiral ligands or metal ions, was constructed for the first time by encapsulating chiral carbon dots (CCDs) and magnetic Fe3O4 nanoparticles into hierarchical porous metal-organic frameworks (HP-MOFs). Fe3O4/CCDs@HP-ZIF-8, which integrates fluorescent chiral property, magnetism, and hierarchical porosity, shows enormous potential in enantiomeric recognition and adsorption. Fluorescence detection results demonstrate that Fe3O4/CCDs@HP-ZIF-8 presents different fluorescence quenching for naproxen enantiomers. The limits of detection are determined to be 0.05 μM for S-naproxen (S-Nap) and 0.30 μM for R-naproxen (R-Nap), respectively. Furthermore, the isothermal, kinetic, and thermodynamic adsorption behaviors of Fe3O4/CCDs@HP-ZIF-8 to naproxen enantiomers were systematically studied. Due to its hierarchical porosity, the composite exhibits higher adsorption capacity to naproxen enantiomers compared to the non-hierarchical porous composite. Studies of enantiomeric recognition and adsorption mechanisms affirm that the synergistic effect of multiple mechanisms exists between Fe3O4/CCDs@HP-ZIF-8 and naproxen enantiomers. Finally, the satisfactory recoveries and relative standard deviations in the actual sample assays demonstrate the practicality of Fe3O4/CCDs@HP-ZIF-8 for S-Nap detection. This non-destructive functionalization method creates an innovative pathway for developing advanced multifunctional chiral materials, holding great promise for enantiomeric recognition and adsorption. 

Fabrication of a bifunctional fluorescent chiral composite based on magnetic Fe3O4/chiral carbon dots@hierarchical porous metal-organic framework.

Construction of WO3 nanocubes@Loess for rapid photocatalytic degradation of organics in wastewater under sunlight

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