Hollow Ni3S4@Co3S4 with core-satellite nanostructure derived from metal-organic framework (MOF)-on-MOF hybrids as an electrode material for supercapacitors.

Metal-organic frameworks (MOFs) have found wide applications in the field of supercapacitors due to their highly controllable porous structure, big specific surface area, and abundant chemical functional groups. MOF-on-MOF hybrids not only enhance the composition of MOFs (such as ligands and/or metal centers) but also provide greater structural diversity. By utilizing MOFs as precursors for preparing sulfides, the unique characteristics and inherent structure of MOFs are preserved but their conductivity and capacitance are enhanced. This study successfully synthesized hollow-structured Ni3S4@Co3S4 derived from an Ni-MOF@ZIF-67 hybrid structure, where the Ni-MOF serves as the core and ZIF-67 as the satellite. The Ni3S4@Co3S4 electrode demonstrated a specific capacity as high as 747.3 C g-1 at 1 A g-1, and it could still maintain 77% of its initial capacity at 10 A g-1. Furthermore, the assembled Ni3S4@Co3S4//AC hybrid supercapacitor (HSC) device achieved a maximum energy density of 30.8 W h kg-1 when the power density was 750 W kg-1. The device exhibited remarkable cycling durability, retaining 85.4% of its initial capacitance after 5000 cycles. Therefore, the derived functional materials based on MOF-on-MOF provide a more scalable and promising approach for the preparation of efficient electrode materials.

Fluorescent sensor based on bismuth metal-organic frameworks (Bi-MOFs) mimic enzyme for H2O2 detection in real samples and distinction of phenylenediamine isomers.

Although peroxidase-like nano-enzymes have been widely utilized in biosensors, nano-enzyme based biosensors are seldom used for both quantitative analysis of H2O2 and differentiation of isomers of organic compounds simultaneously. In this study, a dual-functional mimetic enzyme-based fluorescent sensor was constructed using metal-organic frameworks (Bi-MOFs) with exceptional oxidase activity and fluorescence properties. This mimetic enzyme sensor facilitated quantitative analysis of H2O2 and accurate discrimination of phenylenediamine isomers. The sensor exhibited a wide linear range (0.5-400 µM) and low detection limit (0.16 µM) for the detection of H2O2. Moreover, the sensor can also be used for the discrimination of phenylenediamine isomers, in which the presence of o-phenylenediamine (OPD) leads to the appearance of a new fluorescence emission peak at 555 nm, while the presence of p-phenylenediamine (PPD) significantly quenched its fluorescence due to the internal filtration effect. The proposed strategy exhibited a commendable capability in distinguishing phenylenediamine isomers, thereby paving the way for novel applications of MOFs in the field of environmental science.

A dual-functional fluorescence probe CDs@ZIF-90 for highly specific detection of Al3+ and Hg2+ in environmental water samples.

In recent years, the escalating water pollution has resulted in serious harm to human health and ecological environment due to the excessive discharge of toxic metal ions such as Al3+ and Hg2+. Therefore, it is crucial to develop a simple, efficient, and rapid detection method for monitoring the levels of the metal ions in water environment to ensure public health and ecological safety. In this study, carbon dots (CDs) containing heteroatom Si were successfully synthesized by the solvothermal method. Subsequently, a novel dual-functional fluorescent sensor (CDs@ZIF-90) was constructed by integrating CDs with zeolitic imidazolate framework-90 (ZIF-90). The fluorescent composite CDs@ZIF-90 showed outstanding optical properties and excellent structural and luminescence stability in aqueous medium. Particularly, its fluorescence at 453 nm can be remarkably enhanced by Al3+ and quenched upon exposure to Hg2+. As a result, the CDs@ZIF-90 was applied in sensitive and selective determination of Al3+ and Hg2+ ions with wide linear ranges (1-200 µM and 0.05-240 µM) and low detection limits (0.81 µM and 19.6 nM). Moreover, a convenient and rapid fluorescence test strip was also successfully prepared for visual detection of Al3+ and Hg2+ ions. This work is the first try to use the CDs@ZIF-90 fluorescence sensing material for highly sensitive and selective determination of Al3+ and Hg2+ based on "turn-on" and "turn-off" dual modes, respectively and it provides a new idea for monitoring quality of drinking water and environmental water. It is of great significance for human health and environmental protection.

Rapid detection of the biomarker for cystinuria by a metal-organic framework fluorescent sensor.

Arginine (Arg) is considered a valuable biomarker for various diseases, including cystinuria, and its concentration level holds significant implications for human health. To achieve the purposes of food evaluation and clinical diagnosis, it is imperative to develop a rapid and facile method for selective and sensitive determination of Arg. In this work, a novel fluorescent material (Ag/Eu/CDs@UiO-66) was synthesized by encapsulating carbon dots (CDs), Eu3+ and Ag + into UiO-66. This material can serve as a ratiometric fluorescent probe for detecting Arg. It exhibits a high sensitivity with a detection limit of 0.74 µM and a relatively broad linear range from 0-300 µM. After dispersing the composite Ag/Eu/CDs@UiO-66 in an Arg solution, the red emission of Eu3+ center at 613 nm was significantly enhanced, while the characteristic peak of CDs center at 440 nm remained unchanged. Therefore, a ratio fluorescence probe could be constructed based on the peak height ratio of the two emission peaks to achieve selective detection of Arg. In addition, the remarkable ratiometric luminescence response induced by Arg results in a significant color transition from blue to red under UV-lamp for Ag/Eu/CDs@UiO-66, which was convenient for visual analysis.

Nitrogen-doped carbon dots for sensitive detection of ferric ions and monohydrogen phosphate by the naked eye and imaging in living cells.

Nitrogen doped carbon dots (N-CDs) have been prepared via a one-pot hydrothermal method by using formamide and o-phenylenediamine as the carbon precursors. The as-fabricated N-CDs display excellent water dispersibility, good biocompatibility and anti-photobleaching properties. A strong emission band with an emission maximum (λ fl max) of 556 nm is observed under 450 nm excitation, and a large Stokes shift of 106 nm is presented. However, the fluorescence is quenched by the addition of Fe3+; a good linearity is shown in the range of 0-65 µM with a detection limit as low as 0.85 µM. Fortunately, the quenched fluorescence could be recovered rapidly by the addition of monohydrogen phosphate (HPO4 2-) due to the formation of the stable [N-CDs-Fe3+-HPO4 2-] complex, and a good linearity is exhibited in the range of 0-60 µM with a low detection limit of 0.80 µM for HPO4 2-. A novel "on-off-on" fluorescence response is seen with an obvious color change from yellow-crimson-yellow by the naked eye. In addition, the confocal microscopy images suggest that the as-synthesized N-CDs could serve as a sensitive nanosensor for Fe3+ and HPO4 2- detection, implying the diverse potential application of N-CDs in the biomedical field.

A spiropyran functionalized fluorescent probe for mitochondria targeting and imaging of endogenous hydrogen sulfide in living cells.

A turn-on spiropyran functionalized fluorescein derivative (FMC) is developed for targeting HS- in mitochondria. FMC exhibits very weak fluorescence at 525 nm under the excitation of 470 nm in aqueous solution due to its colorless spiropyran form; upon addition of HS-, a strong fluorescence enhancement by 6.4-fold is observed with spirocycle-opened merocyanine form and rapid trapping kinetics for HS-. FMC has good biocompatibility and high selectivity towards HS- with a detection limit of 88.2 nM and is very sensitive among the reported H2S fluorescent probes. Moreover, the significant colocalization of FMC with Mito Tracker® Deep Red FM in human laryngeal epidermoid carcinoma (HEp-2) cells and the Pearson correlation coefficient of 0.87 together demonstrate that FMC can target and image the endogenous H2S in the mitochondria of living cells.