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The detrimental effect of (NO 2 - ) on environment, a sensitive and selective detection of nitrite (NO 2 - ) ions with point-to-care device is need to be fabricated. Herein, we report the non-enzymatic nitrite sensor using a novel reduced graphene oxide/molybdenum disulfide/poly (3, 4-ethylene dioxythiophene) (rGO/MoS 2 /PEDOT) nanocomposite electrode. The rGO/MoS 2 /PEDOT nanocomposite was synthesized using facile and cost-effective hydrothermal and polymerization approaches. The characteristics of rGO-MoS 2 -PEDOT nanocomposite was investigated by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Raman, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analyses. The rGO-MoS 2 -PEDOT nanocomposite modified glassy carbon electrode (GCE) was directly used for electrocatalytic detection of nitrite ions present in the solution. TEM images show the PEDOT nanoparticles with an average size of 100-120 nm are uniformly covered on the outer face of rGO-MoS 2 nanosheets. The interaction between the PEDOT and rGO-MoS 2 is evidenced in the FTIR, XRD and XPS studies, and they produced synergistic effect, resulting enhanced electrocatalytic performance activity towards oxidation of nitrite. Under optimized conditions, the fabricated electrode exhibited remarkably good sensitivity (874.19 μA μM -1  cm -2 ), low detection limit (LOD) (0.059 μM, S/N = 3), wide linear range (0.001-1 mM) of nitrite with desirable selectivity, long-term stability and reproducibility. Furthermore, the practical feasibility of the fabricated sensor is validated by the successful detection of nitrite ion in some water and milk samples with excellent correlation. Thus, feasible easier synthesis method was adopted first time to fabricate rGO-MoS 2 -PEDOT nanocomposite nitrite sensor in the milk and water samples with enhanced selectivity, sensitivity and LOD., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Development of selective, sensitive and non-enzymatic sensor for glucose determination is highly important for the diagnosis and management of diabetes. Herein, we have reported the novel ultra sensitive and non-enzymatic sensor development by in-situ wraped NiO nanostructures (∼10-15 nm) on the sulfur-doped hollow carbon nanospheres (SDHCNSs) through hydrothermal-assisted process. The structural and morphological properties of the nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) techniques. The prepared NiO@SDHCNSs was directly used as an electrochemical sensor for glucose determination, and its performance was evaluated by cyclic voltammetry and amperometric techniques. The fabricated non-enzymatic biosensor was exhibited remarkably good sensitivity (1697 μA mM -1 cm -2 ), low detection limit (LOD) (52 nM), a wide linear range (up to 13 mM) of glucose with desirable selectivity, stability and reproducibility. Further, the constructed sensor has demonstrated an excellent anti-interference property in the presence of common interferences such as dopamine (DA), uric acid (UA) and ascorbic acid (AA). Most interestingly, the fabricated electrode is applicable for the practical analysis of glucose in the real blood serum and urine samples. The excellent electrochemical performances of NiO@SDHCNSs towards the oxidation of glucose are attributed to the increased electron transfer passage through unique hollow spherical morphology with increased redox couple of Ni(OH) 2 /NiOOH derived from NiO. Thus, the improved electrochemical performances of NiO@SDHCNSs can be adopted as a potential electrode for the real sample analysis., (Copyright © 2018 Elsevier B.V. All rights reserved.)