2020
DOI: 10.1016/j.jallcom.2020.154420
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Nanocrystalline complex oxides NixCo3-xO4: Cations distribution impact on electrical and gas sensor behaviour

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Cited by 8 publications
(9 citation statements)
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“…Further oxidation of surface sulfites to sulfates by reaction (4) serves as an additional source of electrons, which increases the sensor signal at long times. In our previous work [19], it was shown that the concentration of chemisorbed oxygen on the surface of Ni0.1Co2.9O4 is lower than on Co3O4. This leads to a slowdown in the rate of reaction (2) and, as a result, led to a decrease in sensor signal toward 1 ppm H2S with increase in Ni content.…”
Section: Discussionmentioning
confidence: 89%
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“…Further oxidation of surface sulfites to sulfates by reaction (4) serves as an additional source of electrons, which increases the sensor signal at long times. In our previous work [19], it was shown that the concentration of chemisorbed oxygen on the surface of Ni0.1Co2.9O4 is lower than on Co3O4. This leads to a slowdown in the rate of reaction (2) and, as a result, led to a decrease in sensor signal toward 1 ppm H2S with increase in Ni content.…”
Section: Discussionmentioning
confidence: 89%
“…[20]. The phase composition, microstructure parameters and the charge state of cations were studied by XRD, TEM, XPS, EPR, as well as BET measurements [19]. The main characteristics of the samples are presented in Table 1.…”
Section: Nanocrystalline Powders Of Co 3 O 4 and Nimentioning
confidence: 99%
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“…In Figure 2i, the well-defined peaks can be observed for Co-NbO with two g values of 2.012 and 2.052. [30,31] Co doping enables the formation of electron-hole pairs in T-Nb 2 O 5 . The formation of oxygen vacancies resulting from cobalt doping can be described in the following formula…”
Section: Resultsmentioning
confidence: 99%
“…In Figure 2i, the well‐defined peaks can be observed for Co–NbO with two g values of 2.012 and 2.052. [ 30,31 ] Co doping enables the formation of electron‐hole pairs in T–Nb 2 O 5 . The formation of oxygen vacancies resulting from cobalt doping can be described in the following formula Nb2O5CoO()badbreak+22Oobadbreak+3VO··goodbreak+2normalCnormaloNb\begin{equation}{\rm{Nb}}_2{{\rm{O}}}_5\xrightarrow{{{\rm{CoO\ }}\left( { + 2} \right)\ }}2{{\rm{O}}}_{\rm{o}} + 3{\rm{V}}_{\rm{O}}^{ \cdot \cdot } + 2{\rm{C}}{{\rm{o^{\prime\prime\prime}}}}_{{\rm{Nb}}}\end{equation}or Nb2O5Co2O3()badbreak+33Oobadbreak+2VO··goodbreak+2normalCnormaloNb\begin{equation}{\rm{Nb}}_2{{\rm{O}}}_5\xrightarrow{{{\rm{Co}}_2{{\rm{O}}}_3\ \left( { + 3} \right)\ }}3{{\rm{O}}}_{\rm{o}} + 2{\rm{V}}_{\rm{O}}^{ \cdot \cdot } + 2{\rm{C}}{{\rm{o^{\prime\prime}}}}_{{\rm{Nb}}}\end{equation}where O o represents the lattice oxygen, normalVnormalO··${\rm{V}}_{\rm{O}}^{ \cdot \cdot }$ represents the oxygen vacancy with two units of positive charge, Co′′′ Nb and Co′′ Nb denote the substitution of Co atoms in Nb lattice sites with three and two units of negative charge respectively.…”
Section: Resultsmentioning
confidence: 99%