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Analytical chemistry v.89 no.2, 2017년, pp.1267 - 1274   SCI SCIE
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Gold Nanoparticle Modified Transparent Carbon Ultramicroelectrode Arrays for the Selective and Sensitive Electroanalytical Detection of Nitric Oxide

Elliott, Janine (Department of Chemistry, Center for Nano- and Molecular Science and Technology, The University of Texas at Austin, Austin, Texas 78712, ); Duay, Jonathon (Department of Chemistry, Center for Nano- and Molecular Science and Technology, The University of Texas at Austin, Austin, Texas 78712, ); Simoska, Olja (Department of Chemistry, Center for Nano- and Molecular Science and Technology, The University of Texas at Austin, Austin, Texas 78712, ); Shear, Jason B. (Department of Chemistry, Center for Nano- and Molecular Science and Technology, The University of Texas at Austin, Austin, Texas 78712, ); Stevenson, Keith J. (Center for Electrochemical Energy Storage, Skolkovo Institute of Science and Technology, Moscow 143026, );
  • 초록  

    Transparent carbon ultramicroelectrode arrays (T-CUAs) were made using a previously reported facile fabrication method (Duay et al. Anal. Chem. 2015 , 87 , 10109). Two modifications introduced to the T-CUAs were examined for their analytical response to nitric oxide (NO • ). The first modification was the application of a cellulose acetate (CA) gas permeable membrane. Its selectivity to NO • was extensively characterized via chronoamperometry, electrochemical impedance spectroscopy (EIS), and atomic force microscopy (AFM). The thickness of the CA membrane was determined to be 100 nm and 88 ± 15 nm using AFM and EIS, respectively. Furthermore, the partition and diffusion coefficients of NO • within the CA membrane were determined to be 0.0500 and 2.44 × 10 –13 m 2 /s using EIS measurements. The second modification to the 1.54T-CUA was the introduction of chitosan and gold nanoparticles (CS/GNPs) to enhance its catalytic activity, sensitivity, and limit of detection (LOD) to NO • . Square wave voltammetry was used to quantify the NO • concentration at the CA membrane covered 1.54T-CUA with and without CS/GNPs; the LODs were determined to be 0.2 ± 0.1 and 0.44 ± 0.02 μM ( S / N = 3), with sensitivities of 9 ± 9 and 1.2 ± 0.4 nA/μM, respectively. Our results indicate that this modification to the arrays results in a significant catalytic enhancement to the electrochemical oxidation of NO • . Hence, these electrodes allow for the in situ mechanistic and kinetic characterization of electrochemical reactions with high electroanalytical sensitivity. Graphic Abstract ACS Electronic Supporting Info


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