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Ultrafast Detection of Low Acetone Concentration Displayed by Au-Loaded LaFeO3 Nanobelts owing to Synergetic Effects of Porous 1D Morphology and Catalytic Activity of Au Nanoparticles
Author(s) -
Katekani Shingange,
H.C. Swart,
G.H. Mhlongo
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b01989
Subject(s) - porosity , morphology (biology) , acetone , materials science , nanoparticle , chemical engineering , catalysis , ultrashort pulse , nanotechnology , chemistry , composite material , organic chemistry , optics , laser , engineering , genetics , physics , biology
Herein, we report on one-dimensional porous Au-modified LaFeO 3 nanobelts (NBs) with high surface area, which were synthesized through the electrospinning method. The incorporation and coverage of Au nanoparticles (NPs) on the surface of the LaFeO 3 NBs was achieved by adjusting the HAuCl amount in the precursor solution. Successful incorporation of Au NPs was examined by X-ray diffraction, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. The gas-sensing performance of both the pure and Au/LaFeO 3 NB-based sensors was tested toward 2.5-40 ppm of acetone at working temperatures in the range from room temperature to 180 °C. The gas-sensing findings revealed that Au/LaFeO 3 NB-based sensor with the Au concentration of 0.3 wt % displayed improved response of 125-40 ppm of acetone and rapid response and recovery times of 26 and 20 s, respectively, at an optimal working temperature of 100 °C. Furthermore, all sensors demonstrated an excellent response toward acetone and remarkable selectivity against NO 2 , NH 3 , CH 4 , and CO. Hence, the Au/LaFeO 3 -NB-based sensor is a promising candidate for sensitive, ultrafast, and selective acetone detections at low concentrations. The gas-sensing mechanism of the Au/LaFeO 3 sensors is explained in consideration of the catalytic activity of the Au NPs, which served as direct adsorption sites for oxygen and acetone.

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