Converting commonly-used paper into nano-engineered fluorescent biomass-based platform for rapid ClO- quantitative detection in living cells and water sources.

Hypochlorous acid (HClO) and derivative ionic form (ClO-) are significant components of reactive oxygen species, and thus various diseases are correlatively related to the concentration of ClO-. Recently, paper-based indicators have been confirmed to be efficient strategy for sensing hazardous and noxious substances. However, most of these materials can only achieve qualitative detection of the substrates. Herein, an extremely simple manufacturing strategy was proposed to convert commonly-used paper into nano-engineered fluorescent biomass-based platform (CMJL-FP) integrated with on-demand self-assembled colorimetric and ratiometric fluorescence sensor (CMJL) for rapid ClO- quantitative detection in organisms or water sources using smartphones. The CMJL exhibited a highly selective and sensitive ratiometric response to ClO- at a low detection limit (LOD = 92.6 nM). The associating interactions between the fluorescence nano-particles and micro-nano fibers of CMJL-FP ensure good-stability during ClO- detection. It has been experimentally demonstrated that CMJL-FP allows one to realize the rapid quantitative detection of ClO- ions in living cells and large-scale water sources by using color recognition software as part of a simple smartphone. Therefore, integrating the proposed fluorescent paper with smartphones provides an effective, sustainable, cheap and conceptual strategy for quantitative detection of hazardous and noxious substances in organisms and environments.

Preparation of nitrogen-doped carbon quantum dots from chelating agent and used as fluorescent probes for accurate detection of ClO- and Cr(â ¥).

In this study, a novel ionic sensor based on nitrogen-doped carbon quantum dots (N-CQDs) was developed for sensitive detection of hypochlorite ions (ClO-) and dichromate ions (Cr(Ⅵ)) by fluorescence spectrometry. The N-CQDs was synthesized by hydrothermal method using Methyl Glycine Diacetic acid Trisodium Salt (MGDA) and Ethylenediamine (EDA) with bright blue fluorescence, high fluorescence quantum yield, abundant surface groups and good dispersion. The N-CQDs had a remarkable emission characteristic at 450 nm under the ultraviolet light of 350 nm, and the ClO- and Cr(Ⅵ) ions could quantificationally quench the fluorescence of this emission band. The results showed that N-CQDs had broad linear detection range and the detection limits of trace ClO- and Cr(Ⅵ) ions are 5.0 µM and 2.1 µM, respectively. Subsequently, further verify the reliability of this study and the N-CQDs played an excellent role in the ion detection of actual water samples. The quenching mechanism of ClO- is proved to be dominated by static quenching, while the quenching mechanism of Cr(Ⅵ) is mainly due to inner filter effect. This study is envisioned to efficiently prepare N-CQDs with novel raw materials, provide enlightening insights for enriching the detection of various trace ions by CQDs, and open up a new way to use fluorescence characteristics for water detection.

Highly sensitive fluorescent probe for selective detection of hypochlorite ions using nitrogen-fluorine co-doped carbon nanodots.

Hypochlorite ions (ClO-) are widely used in bleaching agents and disinfectants. However, high concentrations of chloride species are harmful to human health. Therefore, effective methods for the detection of ClO- ions are required. In this study, using 4-fluorophthalic acid and glycine, nitrogen-fluorine co-doped carbon nanodots (N,F-CDs) were synthesized by one-pot hydrothermal synthesis for use as a fluorescent probe for the fluorometric detection of ClO- in aqueous media, based on the inhibition of n â†’ π* transitions. The excitation and emission peak centers of the N,F-CDs are at 387 and 545 nm, respectively. The N,F-CDs show a fast quenching response (<1 min) for ClO- and can be used in a wide pH range (pH 4-13). Under optimal conditions, the fluorescence intensity decreased with increase in the ClO- concentration from 0 to 35 µM, and a low limit of detection (9.6 nM) was achieved. This probe possesses excellent selectivity and high sensitivity and was used to analyze standardized samples of piped water, achieving a satisfactory recovery. Thus, this nitrogen-fluorine co-doped nanodot probe is promising for the detection of pollutants.

Development of Triboelectroceutical Fabrics for Potential Applications in Self-Sanitizing Personal Protective Equipment.

Attachment of microbial bodies including the corona virus on the surface of personal protective equipment (PPE) is found to be potential threat of spreading infection. Here, we report the development of a triboelectroceutical fabric (TECF) consisting of commonly available materials, namely, nylon and silicone rubber (SR), for the fabrication of protective gloves on the nitrile platform as model wearable PPE. A small triboelectric device (2 cm × 2 cm) consisting of SR and nylon on nitrile can generate more than 20 V transient or 41 µW output power, which is capable of charging a capacitor up to 65 V in only ∼50 s. The importance of the present work relies on the TECF-led antimicrobial activity through the generation of an electric current in saline water. The fabrication of TECF-based functional prototype gloves can generate hypochlorite ions through the formation of electrolyzed water upon rubbing them with saline water. Further, computational modelling has been employed to reveal the optimum structure and mechanistic pathway of antimicrobial hypochlorite generation. Detailed antimicrobial assays have been performed to establish effectiveness of such TECF-based gloves to reduce the risk from life-threatening pathogen spreading. The present work provides the rationale to consider the studied TECF, or other materials with comparable properties, as a material of choice for the development of self-sanitizing PPE in the fight against microbial infections including COVID-19.

Fluorescence Emission of Polyethylenimine-Derived Polymer Dots and Its Application to Detect Copper and Hypochlorite Ions.

Polymer dots with nonconjugated groups that are facile to synthesize and environmentally friendly generally attract substantial interest. However, their fluorescence-emitting mechanisms are not clear. In this paper, nonconjugated polymer dots (N-PDs) are synthesized by amidation reaction between polyethylenimine (PEI) and citric acid (CA), then self-assemble into rice-like dots in aqueous phase with a high fluorescence quantum yield. Such nitrogen-containing nonconjugated compounds N-PDs are believed to be inherently fluorescent, and the reported reasons for fluorescence-emitting are discussed. Importantly, these N-PDs can be used as an excellent fluorescent probe to detect Cu2+ and ClO- in aqueous solutions. Cu2+ could combine with the PEI moiety of the N-PDs to form a copper amine complex and then quench the fluorescence by an internal filtration effect. ClO- could oxidize the hydroxyl groups on the surface of the N-PDs to form a positive charge, blocking electron transfer between the hydroxyl groups and the chromophore groups. Finally, the sensor was successfully applied to the detection of Cu2+ and ClO- in environmental water samples.