Abstract

The effect of UV illumination on the room temperature electrical detection of ammonium nitrate vapor was examined. The sensor consists of a self-assembled ensemble of silica nanosprings coated with zinc oxide. UV illumination mitigates the baseline drift of the resistance relative to operation under dark conditions. It also lowers the baseline resistance of the sensor by 25% compared to dark conditions. At high ammonium nitrate concentrations (120 ppm), the recovery time after exposure is virtually identical with or without UV illumination. At low ammonium nitrate concentrations (20 ppm), UV illumination assists with refreshing of the sensor by stimulating analyte desorption, thereby enabling the sensor to return to its baseline resistance. Under dark conditions and low ammonium nitrate concentrations, residual analyte builds up with each exposure, which inhibits the sensor from returning to its original baseline resistance and subsequently impedes sensing due to permanent occupation of absorption sites.

Highlights

  • Detection and sensing of chemical hazards, improvised explosive devices, etc., is the first line of defense and the most effective approach for minimizing their threat to human health and safety.Toxic or dangerous agents produce vapors that, if accurately detected, serve as signatures of the products

  • The morphology of the silica nanosprings and the Zinc oxide (ZnO) coating were determined with scanning

  • We examined the effect of UV illumination on the responsiveness of a ZnO-coated nanospring sensor to ammonium nitrate vapor operated at room temperature

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Summary

Introduction

Toxic or dangerous agents produce vapors that, if accurately detected, serve as signatures of the products. For these reasons, it is imperative to develop sensors that can effectively detect harmful gases in real time at parts per billion concentrations, have few false positives, have fast recovery and are refreshable. The response of a ZnO-based vapor sensor to a target analyte is a change in its conductance or resistance. Such changes in the resistance are attributed to analyte-induced variations of the width of the space charge near the surface of the semiconductor [9]

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