2017
DOI: 10.1016/j.snb.2017.06.040
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Synthesis of Ni-doped α-MoO3 nanolamella and their improved gas sensing properties

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Cited by 69 publications
(15 citation statements)
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“…As shown in Figure a, the Mo 3 d core‐level spectrum is dominated by the Mo 3 d 5/2 and 3 d 3/2 doublet at 233.3 and 236.4 eV, respectively, which are associated with the Mo 6+ oxidation state. [ 78 ] In addition, the peak fitting reveals minor shoulders at 235.2 eV, which are ascribed to the 3 d doublet of reduced Mo 5+ (blue line), commonly observed in thermally grown MoO 3 due to the prevalence of native defects (e.g., oxygen vacancies). [ 79 ] However, it should be noted that the ratio of Mo 5+ /Mo 6+ is less than 3.7%, indicating that the amount of nonstoichiometric MoO 3 is marginal.…”
Section: Resultsmentioning
confidence: 99%
“…As shown in Figure a, the Mo 3 d core‐level spectrum is dominated by the Mo 3 d 5/2 and 3 d 3/2 doublet at 233.3 and 236.4 eV, respectively, which are associated with the Mo 6+ oxidation state. [ 78 ] In addition, the peak fitting reveals minor shoulders at 235.2 eV, which are ascribed to the 3 d doublet of reduced Mo 5+ (blue line), commonly observed in thermally grown MoO 3 due to the prevalence of native defects (e.g., oxygen vacancies). [ 79 ] However, it should be noted that the ratio of Mo 5+ /Mo 6+ is less than 3.7%, indicating that the amount of nonstoichiometric MoO 3 is marginal.…”
Section: Resultsmentioning
confidence: 99%
“…The chemical states of Mo and O atoms in α‐MoO 3 were investigated by XPS spectrum. Mo is in its highest oxidation state of +6 as indicated by Mo 3d 5/2 (BE = 233.1 eV) and Mo 3d 3/2 (BE = 236.2 eV) (Figure A) . The appearance of Mo 3d 5/2 (BE = 234.3 eV) and Mo 3d 3/2 (BE = 237.5 eV) may be ascribed to the existence of Mo 2+ .…”
Section: Resultsmentioning
confidence: 96%
“…However, for MOS gas sensing materials, the number of the surface active site of the sensing materials is almost constant at a certain operating temperature. Therefore, the sensor response would gradually become saturated with the further increase of H 2 S concentration for the reason that there are no more active sites available for the adsorption and reaction of H 2 S molecules [44,45]. Specifically, it is worth mentioning that the sensor still exhibits a notable response of 1.5 at a relatively low H 2 S concentration of 50 ppb, indicating a promising application potential in the monitoring of trace amount of H 2 S.…”
Section: Resultsmentioning
confidence: 99%