Morphology Adjustment and Optimization of CuS as Enzyme Mimics for the High Efficient Colorimetric Determination of Cr(VI) in Water

Metal sulfide is often utilized as a catalyzed material to form colorimetric response system for some heavy metal detection. While the aggregation effect and conventional morphology limited the catalyzed efficiency. Herein, a robust method based on morphology adjustment was proposed to improve the dispersibility and catalytic performance of CuS. The results demonstrated when the solvent ratio of ethylene glycol and dimethyl sulfoxide arrived at 3:1, it displayed an optimal structure which is like a patulous flower. Meanwhile, an optimal surface binding energy (ΔE) of 120.1 kcal/mol was obtained via theoretical calculation model. The flower-like structure caused a 2-fold increase in the catalytic level. Subsequently, the CuS was employed to make colorimetric detection of Cr(VI) in water. The assay results exhibited a linear range of the Cr(VI) from 60 to 340 nM, the limit of detection was 1.07 nM. In the practical tests for Qianhu lake water, the spiked recoveries were 93.6% and 104% with the RSD of 4.71% and 3.08%. Therefore, this CuS-based colorimetric method possesses a satisfactory application prospect for the Cr(VI) determination in water

Morphology Adjustment and Optimization of CuS as Enzyme Mimics for the High Efficient Colorimetric Determination of Cr(VI) in Water

Metal sulfide is often utilized as a catalyzed material to form colorimetric response system for some heavy metal detection. While the aggregation effect and conventional morphology limited the catalyzed efficiency. Herein, a robust method based on morphology adjustment was proposed to improve the dispersibility and catalytic performance of CuS. The results demonstrated when the solvent ratio of ethylene glycol and dimethyl sulfoxide arrived at 3:1, it displayed an optimal structure which is like a patulous flower. Meanwhile, an optimal surface binding energy (ΔE) of 120.1 kcal/mol was obtained via theoretical calculation model. The flower-like structure caused a 2-fold increase in the catalytic level. Subsequently, the CuS was employed to make colorimetric detection of Cr(VI) in water. The assay results exhibited a linear range of the Cr(VI) from 60 to 340 nM, the limit of detection was 1.07 nM. In the practical tests for Qianhu lake water, the spiked recoveries were 93.6% and 104% with the RSD of 4.71% and 3.08%. Therefore, this CuS-based colorimetric method possesses a satisfactory application prospect for the Cr(VI) determination in water

Dual Application: p-CuS/n-ZnS Nanocomposite Construction for High-Efficiency Colorimetric Determination and Photocatalytic Degradation of Tetracycline in Water

Herein, CuS was incorporated with ZnS to form a novel nanocomposite via cation exchange, and the product was then employed for dual application of the colorimetric determination and photocatalytic degradation of tetracycline (TC) in water. The formed p–n heterojunction provided an improved gap width and electron mobility, which could rapidly catalyze H2O2 to produce plenty of •OH, supporting a color conversion with TMB. Meanwhile, the addition of TC could lead to the further enhancement in colorimetric signal, and the distinction level was sensitive to the target amount. Additionally, under light conditions, the p-CuS/n-ZnS could produce •O2−, •OH, and h+ through photocatalysis, and these ions could degrade the TC via oxidation. In the colorimetric determination of TC, the signal responses were obtained within 10 min, and the detection limit was 20.94 nM. The recovery rates were 99% and 106% for the water samples from Ganjiang river. In the photocatalytic degradation, the TC was degraded by 91% within 120 min, which was threefold that of ZnS. Meanwhile, the morphology feature of the p-CuS/n-ZnS remained after multiple uses, suggesting a favorable material stability. This strategy provides application prospects for the monitoring and control of antibiotics in water

In-situ Growth of NiCo Layered Double Hydroxide Nanocages on Co Foams as Efficient Electrocatalysts for Water Splitting: A Rational Design Approach

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Dual-Readout Immunochromatographic Assay by Utilizing MnO₂ Nanoflowers as the Unique Colorimetric/Chemiluminescent Probe

Manganese dioxide nanoflowers (MnO₂ NFs) were synthesized and used as a dual readout probe to develop a novel immunochromatographic test strip (ITS) for detecting pesticide residues using chlorpyrifos as the model analyte. MnO₂ NFs-labeled antibody for chlorpyrifos was employed as the signal tracer for conducting the ITS. After 10 min competitive immunoreaction, the tracer antibody was captured by the immobilized immunogen in the test strip, resulting in the captured MnO₂ NFs on test line. The captured MnO₂ NFs led to the appearance of brown color on the test line, which could be easily observed by the naked eye as a qualitative readout. Due to the very slight colorimetric difference of chlorpyrifos at trace concentrations, the semiquantitative readout by naked eyes could not meet the demand of quantitative analysis. MnO₂ NFs showed a significant effect on the luminol–H₂O₂ chemiluminescent (CL) system, and the CL signal driven by MnO₂ NFs were used to detect the trace concentration of chlorpyrifos quantitatively. 1,3-Diphenylisobenzofuran quenching studies and TMB–H₂O₂ coloration assays were conducted for studying the enhancing mechanism of MnO₂ NFs, which was based on the oxidant activity to decompose H₂O₂ for forming reactive oxygen species. Under optimal conditions, the linear range of chlorpyrifos was 0.1–50 ng/mL with a low detection limit of 0.033 ng/mL (S/N = 3). The reliability of the dual-readout ITS was successfully demonstrated by the application on traditional Chinese medicine and environmental water samples. Due to the simultaneous rapid-qualitative and sensitive-quantitative detection, the dual-readout protocol provides a promising strategy for rapid screening and field assay on various areas such as environmental monitoring and food safety