2019
DOI: 10.1007/s10971-019-05162-5
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Influence of nickel and lanthanum ions co-doping on photocatalytic properties of TiO2 for effective degradation of reactive yellow 145 in the visible region

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Cited by 34 publications
(24 citation statements)
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“…Hence, the conductivity of titanium dioxide increased by approximately 100-fold after the incorporation of nickel dopant. In accordance with [ 45 ], this can be explained by the generation of a localized Ni 3 d energy state within the TiO 2 (B) band structure. It is important to note that the electronic properties of titanium dioxide were improved steadily up to Ni/Ti = 0.05, while a subsequent extension in nickel content (Ni/Ti = 0.08) was accompanied by a decrease in conductivity.…”
Section: Resultssupporting
confidence: 83%
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“…Hence, the conductivity of titanium dioxide increased by approximately 100-fold after the incorporation of nickel dopant. In accordance with [ 45 ], this can be explained by the generation of a localized Ni 3 d energy state within the TiO 2 (B) band structure. It is important to note that the electronic properties of titanium dioxide were improved steadily up to Ni/Ti = 0.05, while a subsequent extension in nickel content (Ni/Ti = 0.08) was accompanied by a decrease in conductivity.…”
Section: Resultssupporting
confidence: 83%
“…The data obviously reveal changes in the absorbance curve, with a shift in the absorption edge to the visible-light region for nickel-containing TiO2(B) nanobelts. According to previous reports [45,47], this red shift may be related to the appearance of Ni 3d energy levels in the middle of the TiO2 band gap. Furthermore, the spectrum of the TO-Ni-05 sample showed an absorption peak with a maximum at approximately 725 nm, the intensity of which strongly depended on nickel concentration (Figure S5, Supplementary Materials).…”
Section: Resultssupporting
confidence: 64%
“…The value of ν associated with Ti–O bond vibrations depends on the strength of the bond, as reflected by its force constant k , where the bond strength increases with increasing k . However, the introduction of Vo defects decreases the concentration of O atoms available for forming Ti–O bonds, which reduces the value of k . Accordingly, the shift, as observed in Figure b, can be correlated with the Ti–O bond strength, according to the following equation where μ is the reduced mass of the bond acting between the elements.…”
Section: Resultsmentioning
confidence: 99%
“…The total effect of RGO in improving and reducing the photoactivity of Fe 3 O 4 –FeVO 4 can attributed to the following reasons: the improving resulted due to the effect of RGO in acceleration the transition of electrons to the catalyst surface leading inhibition of the photogeneration charges recombination 20 . Also, the addition of RGO facilitated the transition of electrons from VB to CB due to creation of new levels of energy through the E g of Fe 3 O 4 –FeVO 4 which in turn reduced the required energy for this transfer 53 . On the other hand, the reduction in the photoactivity of Fe 3 O 4 –FeVO 4 in the existence of high amount of RGO resulted from the shielding effect of RGO which restrained the absorption of incident photons to arrival at the active sites on the surface of Fe 3 O 4 –FeVO 4 20 .…”
Section: Resultsmentioning
confidence: 99%