4.6 Article

Light-Regulated Electrochemical Sensor Array for Efficiently Discriminating Hazardous Gases

Journal

ACS SENSORS
Volume 2, Issue 10, Pages 1467-1473

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.7b00423

Keywords

light-regulated electrochemical reaction; gas sensor; illumination; discrimation features; PCA pattern recognition algorithm

Funding

  1. Research Award Found [ZX2017000001]
  2. K. C. Wong Magna Fund in Ningbo University
  3. Natural Science Foundation of Ningbo City [2017A610229]
  4. National Natural Science Foundation of China [61771267, 61301050, 61601253, 5161556]
  5. [ZX2016000638]
  6. [ZX201600068076]

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Inadequate detection limit and unsatisfactory discrimination features remain the challenging issues for the widely applied electrochemical gas sensors. Quite recently, we confirmed that light-regulated electrochemical reaction significantly enhanced the electrocatalytic activity, and thereby can potentially extend the detection limit to the parts per billion (ppb) level. Nevertheless, impact of the light-regulated electrochemical reaction on response selectivity has been discussed less. Herein, we systematically report on the effect of illumination on discrimination features via design and fabrication of a light-regulated electrochemical sensor array. Upon illumination (light on), response signal to the examined gases (C3H6, NO, and CO) is selectively enhanced, resulting in the sensor array demonstrating disparate response patterns when compared with that of the sensor array operated at light off. Through processing all the response patterns derived from both light on and light off with a pattern recognition algorithm, a satisfactory discrimination feature is observed. In contrast, apparent mutual interference between NO and CO is found when the sensor array is solely operated without illumination. The impact mechanism of the illumination is studied and it is deduced that the effect of the illumination on the discriminating features can be mainly attributed to the competition of electrocatalytic activity and gas-phase reactivity. If the enhanced electrocatalytic activity (to specific gas) dominates the whole sensing progress, enhancements in the corresponding response signal would be observed upon illumination. Otherwise, illumination gives a negligible impact. Hence, the response signal to part of the examined gases is selectively enhanced by illumination. Conclusively, light-regulated electrochemical reaction would provide an efficient approach to designing future smart sensing devices.

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