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Abstract: In the current work, CuO nanoparticles were synthesized in a facile way, and characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and thermogravimetry. Using these CuO nanoparticles, CuO functionalized QCM resonators were fabricated and explored for HCN sensing. The sensing properties were studied by a sensor characterization system coupled with a mass spectrometer. The sensor response to HCN (+347Hz) was found to be in an opposite direction as compared with other common volatile substances (ether: −1230Hz; water: −1815Hz; n-hexane: −2100Hz; benzene: −3410Hz; acetic acid: −4840Hz; ethanol: −6270Hz), offering excellent selectivity for HCN detection. In addition, the sensitivity (15.1Hz/μg) was very high, and the response (30s) and recovery (750s) were very fast. A sensing mechanism was proposed based on experimental results, in which a surface redox reaction occurs between CuO and Cu2O on the nanoparticle reversibly upon contact with HCN and air, respectively. The current results would provide an exciting alternative to fast, sensitive and selective detection of trace HCN, which would be of particular benefit in the area of public security and environmental applications. [Copyright &y& Elsevier]

Copper oxide nanoparticles were prepared by the solvothermal method, and characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and nitrogen adsorption-desorption measurements. The as-prepared CuO nanoparticles functionalized QCM resonators were fabricated and explored for HCN sensing under varied humidity conditions. When the humidity of air containing HCN is the same as that of environmental air, a characteristic positive frequency shift of CuO nanoparticles functionalized QCM resonator is always observed towards HCN because of a reversible surface redox reaction between CuO and HCN. The sensitivity of CuO nanoparticles functionalized QCM resonators increases with increase of relative humidity in the range of 9-51%. These results provide an important guidance for further developing HCN gas sensors towards practical applications. [ABSTRACT FROM AUTHOR]

Abstract: A novel biosensor is developed based on immobilization of proteins on nanoflake-like SnS2 modified glass carbon electrode (GCE). With glucose oxidase (GOD) as a model, direct electrochemistry of the GOD/nanoflake-like SnS2 is studied. The prepared SnS2 has large surface area and can offer favorable microenvironment for facilitating the electron transfer between protein and electrode surface. The properties of GOD/SnS2 are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV–vis spectroscopy, Fourier transform infrared spectroscopy (FTIR) and cyclic voltammetry (CV), respectively. The immobilized enzyme on nanoflake-like SnS2 retains its native structure and bioactivity and exhibits a surface-controlled, reversible two-proton and two-electron transfer reaction with the apparent electron transfer rate constant (k s) of 3.68s−1. The proposed biosensor shows fast amperometric response (8s) to glucose with a wide linear range from 2.5×10−5 M to 1.1×10−3 M, a low detection limit of 1.0×10−5 M at signal-to-noise of 3 and good sensitivity (7.6±0.5mAM−1 cm−2). The resulting biosensor has acceptable operational stability, good reproducibility and excellent selectivity and can be successfully applied in the reagentless glucose sensing at −0.45V. It should be worthwhile noting that it opens a new avenue for fabricating excellent electrochemical biosensor. [Copyright &y& Elsevier]