2016
DOI: 10.1166/jnn.2016.12892
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Flower-Like ZnO Nanostructure for NO Sensing at Room Temperature

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Cited by 5 publications
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“…In this study, because the optimal T w is approximately 90 °C, the dominant oxygen species is considered to be O 2(ads) – . Normally, when the sensing materials are exposed to NO, the increase of the resistance in the ZnO nanoparticles (n-type) and the decrease of the resistance in the N-rGO or rGO (p-type in our experiments) are expected. The details of adsorption and the reaction process between NO and O 2(ads) – are listed in eqs and .…”
Section: Gas-sensing Properties and Potential Mechanismsmentioning
confidence: 73%
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“…In this study, because the optimal T w is approximately 90 °C, the dominant oxygen species is considered to be O 2(ads) – . Normally, when the sensing materials are exposed to NO, the increase of the resistance in the ZnO nanoparticles (n-type) and the decrease of the resistance in the N-rGO or rGO (p-type in our experiments) are expected. The details of adsorption and the reaction process between NO and O 2(ads) – are listed in eqs and .…”
Section: Gas-sensing Properties and Potential Mechanismsmentioning
confidence: 73%
“…In this study, because the optimal T w is approximately 90 °C, the dominant oxygen species is considered to be O 2(ads) − . Normally, when the sensing materials are exposed to NO, the increase of the resistance in the ZnO nanoparticles (n-type) 56 O 2(ads) − are listed in eqs 4 and 5. Also, as shown in eq 8, when H 2 , a reducing gas meets the sensing material, an opposite electrontransfer process and phenomenon, that is, a decrease in resistance for ZnO nanoparticles and an increase in resistance for N-rGO or rGO are anticipated.…”
Section: Resultsmentioning
confidence: 99%
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“…A slight increase in peak potential is observed with increasing concentration due to changes in the dielectric constant, with analyte being used as an electrolyte. The increase in the peak current can be attributed to the increased ionic strength at the electrode-electrolyte interface, and hence the extent of the electro-catalytic reaction occurring at the surface of the modified electrode [ 58 , 59 , 60 , 61 ] (schematically shown later in Figure 9).…”
Section: Resultsmentioning
confidence: 99%