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Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection
In the present work, three kinds of nanosized SnO(2) samples were successfully synthesized via a hydrothermal method with subsequent calcination at temperatures of 500 °C, 600 °C, and 700 °C. The morphology and structure of the as-prepared samples were characterized using X-ray diffraction, transmis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609542/ https://www.ncbi.nlm.nih.gov/pubmed/37894623 http://dx.doi.org/10.3390/molecules28207143 |
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author | Fan, Bin Zhang, Jing-Ru Chen, Jia-Liang Yang, Ze-Tao Li, Bin Wang, Lin Ye, Mai Zhang, Lu-Lu |
author_facet | Fan, Bin Zhang, Jing-Ru Chen, Jia-Liang Yang, Ze-Tao Li, Bin Wang, Lin Ye, Mai Zhang, Lu-Lu |
author_sort | Fan, Bin |
collection | PubMed |
description | In the present work, three kinds of nanosized SnO(2) samples were successfully synthesized via a hydrothermal method with subsequent calcination at temperatures of 500 °C, 600 °C, and 700 °C. The morphology and structure of the as-prepared samples were characterized using X-ray diffraction, transmission electron microscopy, selected area electron diffraction, Brunauer–Emmett–Teller analysis, and X-ray photoelectron spectroscopy. The results clearly indicated that the SnO(2) sample calcined at 600 °C had a higher amount of chemisorbed oxygen than the SnO(2) samples calcined at 500 °C and 700 °C. Gas sensing investigations revealed that the cataluminescence (CTL) sensors based on the three SnO(2) samples all exhibited high selectivity toward H(2)S, but the sensor based on SnO(2)−600 °C exhibited the highest response under the same conditions. At an operating temperature of 210 °C, the SnO(2)−600 °C sensor showed a good linear response to H(2)S in the concentration range of 20–420 ppm, with a detection limit of 8 ppm. The response and recovery times were 3.5 s/1.5 s for H(2)S gas within the linear range. The study on the sensing mechanism indicated that H(2)S was oxidized into excited states of SO(2) by chemisorbed oxygen on the SnO(2) surface, which was mainly responsible for CTL emission. The chemisorbed oxygen played an important role in the oxidation of H(2)S, and, as such, the reason for the SnO(2)−600 °C sensor showing the highest response could be ascribed to the highest amount of chemisorbed oxygen on its surface. The proposed SnO(2)-based gas sensor has great potential for the rapid monitoring of H(2)S. |
format | Online Article Text |
id | pubmed-10609542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106095422023-10-28 Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection Fan, Bin Zhang, Jing-Ru Chen, Jia-Liang Yang, Ze-Tao Li, Bin Wang, Lin Ye, Mai Zhang, Lu-Lu Molecules Article In the present work, three kinds of nanosized SnO(2) samples were successfully synthesized via a hydrothermal method with subsequent calcination at temperatures of 500 °C, 600 °C, and 700 °C. The morphology and structure of the as-prepared samples were characterized using X-ray diffraction, transmission electron microscopy, selected area electron diffraction, Brunauer–Emmett–Teller analysis, and X-ray photoelectron spectroscopy. The results clearly indicated that the SnO(2) sample calcined at 600 °C had a higher amount of chemisorbed oxygen than the SnO(2) samples calcined at 500 °C and 700 °C. Gas sensing investigations revealed that the cataluminescence (CTL) sensors based on the three SnO(2) samples all exhibited high selectivity toward H(2)S, but the sensor based on SnO(2)−600 °C exhibited the highest response under the same conditions. At an operating temperature of 210 °C, the SnO(2)−600 °C sensor showed a good linear response to H(2)S in the concentration range of 20–420 ppm, with a detection limit of 8 ppm. The response and recovery times were 3.5 s/1.5 s for H(2)S gas within the linear range. The study on the sensing mechanism indicated that H(2)S was oxidized into excited states of SO(2) by chemisorbed oxygen on the SnO(2) surface, which was mainly responsible for CTL emission. The chemisorbed oxygen played an important role in the oxidation of H(2)S, and, as such, the reason for the SnO(2)−600 °C sensor showing the highest response could be ascribed to the highest amount of chemisorbed oxygen on its surface. The proposed SnO(2)-based gas sensor has great potential for the rapid monitoring of H(2)S. MDPI 2023-10-18 /pmc/articles/PMC10609542/ /pubmed/37894623 http://dx.doi.org/10.3390/molecules28207143 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fan, Bin Zhang, Jing-Ru Chen, Jia-Liang Yang, Ze-Tao Li, Bin Wang, Lin Ye, Mai Zhang, Lu-Lu Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title | Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title_full | Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title_fullStr | Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title_full_unstemmed | Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title_short | Highly Selective and Fast Response/Recovery Cataluminescence Sensor Based on SnO(2) for H(2)S Detection |
title_sort | highly selective and fast response/recovery cataluminescence sensor based on sno(2) for h(2)s detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609542/ https://www.ncbi.nlm.nih.gov/pubmed/37894623 http://dx.doi.org/10.3390/molecules28207143 |
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