2017
DOI: 10.1016/j.apsusc.2017.05.166
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Enhanced H 2 S Sensing Performance of a p -type Semiconducting PdO-NiO Nanoscale Heteromixture

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Cited by 35 publications
(7 citation statements)
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“…In PdO–NiO mixed metal oxide, The intense diffraction peaks at 2θ = 37.16, 43.24, 62.81, 75.32 and 79.34° indexed to (101), (012), (110), (113) and (202) planes of the cubic phase of NiO, which is highly consistent with standard JCPDS NO: 01-071-4751 20 . On the other hand, the sharp peaks at 2θ = 34.54 and 55.79° indexed to (101) and (112) planes corresponding to the tetragonal crystalline phase of PdO with an average lattice parameter 3.043 Å, which is highly associated with standard JCPDS NO: 043-1024 21 . Interestingly, metallic diffraction peaks and other impurity phases were not observed in the hybrid PdO–NiO nanocomposite.…”
Section: Resultsmentioning
confidence: 99%
“…In PdO–NiO mixed metal oxide, The intense diffraction peaks at 2θ = 37.16, 43.24, 62.81, 75.32 and 79.34° indexed to (101), (012), (110), (113) and (202) planes of the cubic phase of NiO, which is highly consistent with standard JCPDS NO: 01-071-4751 20 . On the other hand, the sharp peaks at 2θ = 34.54 and 55.79° indexed to (101) and (112) planes corresponding to the tetragonal crystalline phase of PdO with an average lattice parameter 3.043 Å, which is highly associated with standard JCPDS NO: 043-1024 21 . Interestingly, metallic diffraction peaks and other impurity phases were not observed in the hybrid PdO–NiO nanocomposite.…”
Section: Resultsmentioning
confidence: 99%
“…Herein, the green emission with a shorter wavelength of 493 nm represents the oxygen vacancy (O v ) and oxygen antisite (O Ti ); the yellow emission peak found at 585 nm has been associated with interstitial oxygen (O i ). Further, the red emission peak at 613 nm may denote different vacancy states such as titanium interstitial to titanium vacancies, titanium interstitial to oxygen interstitial, and titanium interstitial to oxygen vacancies. , …”
Section: Resultsmentioning
confidence: 99%
“…There have been many reports on Suzuki coupling reaction which proposing that the catalytic active site is a pd(0) species, and in cases where Pd(II) is applied this is the general believe that in situ reduction of Pd(II) to Pd(0) occurs during the reaction. On the basis of this mechanism, in catalytic systems where Pd and PdO and sometimes promoters such as NiO are present simultaneously, the conversion between PdO and Pd is the starting point in the Suzuki coupling reaction, and this has been stated as the equilibrium between PdO and Pd nanoparticles in the most of the published works up to date, and the presence of O 2 in the reaction media prevents the formation of Pd(0) with a tendency to agglomeration by shifting the equilibrium toward Pd(II) . Elaboration of this point of view might be informative because the nature of active sites on Pd for oxidative addition of aryl halide has remained as a subject of debates despite extensive research on the Suzuki‐Miyaura coupling reaction.…”
Section: Resultsmentioning
confidence: 99%