2015
DOI: 10.1016/j.ijleo.2015.06.026
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Structural, diffused reflectance and photoluminescence study of cerium doped ZnO nanoparticles synthesized through simple sol–gel method

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Cited by 40 publications
(13 citation statements)
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“…Higher concentrations of Ce could produce the accumulation of Ce atoms in or near the boundary of ZnO NPs, resulting in a decreased diffusion rate, which prevents the growth of NPs, so that the CS decreases gradually. This phenomenon has also been observed in other studies [17,18]. Based on XRD data, the lattice parameters have been calculated from 1/d(hkl) 2 = [(h 2 + k 2 + hk)/a 2 ] + l 2 /c 2 , where dhkl is the inter-planar distance, (hkl) are the Miller indexes and 'a' and 'c' are lattice constants.…”
Section: Resultssupporting
confidence: 71%
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“…Higher concentrations of Ce could produce the accumulation of Ce atoms in or near the boundary of ZnO NPs, resulting in a decreased diffusion rate, which prevents the growth of NPs, so that the CS decreases gradually. This phenomenon has also been observed in other studies [17,18]. Based on XRD data, the lattice parameters have been calculated from 1/d(hkl) 2 = [(h 2 + k 2 + hk)/a 2 ] + l 2 /c 2 , where dhkl is the inter-planar distance, (hkl) are the Miller indexes and 'a' and 'c' are lattice constants.…”
Section: Resultssupporting
confidence: 71%
“…Such prospects have led to extensive studies of many aspects of Ce-doped ZnO (CZO), motivated by the interest in generating new and unique technologies for manufacturing high-quality doped nanomaterials to obtain enhanced catalysts. Due to the attractive properties and potential applications of CZO nanoparticles (NPs), a variety of preparation techniques have been reported, notable examples include, the electrospinning method [12], sonochemical synthesis [13], microwave-assisted synthesis [14], the combustion method [15], the vapor-solid method [16], the sol-gel method [17][18][19], the magnetron sputtering method [20], and many others [21][22][23][24]. However, most of the reported methods are time-consuming, require complicated equipment with expensive chemical precursors, and operate only under particular and controlled reaction conditions such as pH, growth time, concentration, atmosphere, etc.…”
Section: Introductionmentioning
confidence: 99%
“…This green emission band is due to the formation of oxygen vacancies by the presence of MoO 3 oxide in the structure of the target nanostructures and the presence of some intrinsic defects in the ZnO structure. Generally, the intrinsic defects in ZnO include oxygen vacancies (V o ), zinc vacancies (V Zn ) oxygen (O i ), zinc (Zn i ) interstitials, and defect states dominating the emission in the visible range [ 24 ]. It was observed from Figure 7 that the emission intensity is considerably enhanced with the addition of MoO 3 as compared to the free ZnO sample.…”
Section: Resultsmentioning
confidence: 99%
“…The UV emission bands It can be seen that the emission spectra corresponding to sample M1 (CAB/ZnO) show several emission bands at 327 nm, 391 nm, 421 nm, 444 nm, and 484 nm, respectively. The UV emission bands from 327 nm (Figure 7a) and 350 nm (Figure 7b) can be assigned the near band edge (NBE) emission, and may be due to free exciton recombination [43]. It is known that the emission bands in the visible spectrum are due to different intrinsic defects of ZnO nanostructures, which include oxygen vacancies (V O ), zinc vacancies (V Zn ), oxygen interstitials (O i ), zinc interstitials (Zn i ) and oxygen antisites (O Zn ) [27].…”
Section: Photoluminescence Studymentioning
confidence: 99%