4.8 Article

Plasmon-Induced Enhancement in Analytical Performance Based on Gold Nanoparticles Deposited on TiO2 Film

Journal

ANALYTICAL CHEMISTRY
Volume 81, Issue 17, Pages 7243-7247

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac900894p

Keywords

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Funding

  1. Program for New Century Excellent Talents in University [NCET-06-0380]
  2. State Education Ministry, China, and Nanometer Science Foundation of Shanghai [0952 nm04900]

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This paper demonstrates a novel approach for developing the analytical performance of electrochemical biosensors in which hydrogen peroxide (H2O2) is selected as a model target, based on surface plasmon resonance of gold nanoparticles (Au NPs) deposited onto a TiO2 nanoneedle film. Direct electron transfer of cytochrome c (cyt. c) is realized at Au NPs deposited onto a TiO2 nanoneedle film (Au/TiO2 film), and both anodic and cathodic currents of the redox reaction at the Au/TiO2 film upon visible-light irradiation are amplified. Meanwhile, in the presence of oxidized or reduced states of cyt. c, cathodic or anodic photocurrents are generated respectively by the Au/TiO2 film, Suggesting that the amplified anodic and cathodic currents are ascribed to the visible-light excitation. The photocurrent action spectrum obtained at the Au/TiO2 film in the presence of cyt. c is in a good agreement with the surface plasmon absorption spectrum of Au NPs deposited onto the TiO2 film, and maximum photocurrent is also consistent with the plasmon absorption peak of Au NPs themselves. It indicates that the enhanced photocurrents generated by visible-light irradiation are attributed to the surface plasmon resonance of Au NPs. On the other hand, experimental results reveal that cyt. c is stably immobilized onto the Au/TiO2 film and maintains inherent enzymatic activity toward H2O2 even under continuous visible-light illumination. The amplified redox currents of cyt. c produced by surface plasmon resonance of Au NPs, combined with the stability and enzymatic activity of cyt. c confined on the Au/TiO2 film even after continuous visible-light illumination, subsequently provide the enhanced analytical performance in determination of H2O2. The sensitivity of the present biosensor for H2O2 is 4-fold larger than that obtained without visible-light irradiation, the detection limit is achieved to be 4.5 x 10(-8) M and the dynamic detection linear range extends from 1 x 10(-7) M to 1.2 x 10(-2) M.

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