2007
DOI: 10.1103/physrevb.75.125303
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Origin of luminescence fromGa2O3nanostructures studied using x-ray absorption and luminescence spectroscopy

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Cited by 57 publications
(45 citation statements)
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“…In case of Ga 2 O 3 nanocrystalline film, the relative intensity of UV luminescence (370 nm) is greater than that of blue luminescence (445 nm) while, in case of 700 • C annealed film the blue luminescence is stronger than that of UV luminescence. The affinity of AOT/Ga 2 O 3 nanoparticles is high and therefore the surfactant molecules are bound to the surface of nanoparticles for as deposited Ga 2 O 3 nanocrystalline film, which may result in the reduction of intensity of the emission from the core (blue luminescence) and enhances the intensity of the emission from impurity phase (UV luminescence) rather than the dominantly crystalline β-phase [38]. However, 700 • C annealed film, AOT molecules were burnt out and as a result the intensity of blue luminescence increases as shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…In case of Ga 2 O 3 nanocrystalline film, the relative intensity of UV luminescence (370 nm) is greater than that of blue luminescence (445 nm) while, in case of 700 • C annealed film the blue luminescence is stronger than that of UV luminescence. The affinity of AOT/Ga 2 O 3 nanoparticles is high and therefore the surfactant molecules are bound to the surface of nanoparticles for as deposited Ga 2 O 3 nanocrystalline film, which may result in the reduction of intensity of the emission from the core (blue luminescence) and enhances the intensity of the emission from impurity phase (UV luminescence) rather than the dominantly crystalline β-phase [38]. However, 700 • C annealed film, AOT molecules were burnt out and as a result the intensity of blue luminescence increases as shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…26 It has successfully been used to study the chemical origin of luminescence in porous Si, Si nanowires, SnO 2 nano-ribbons, Ga 2 O 3 nanostructures, and ZnS nanostructures as well as ZnO-ZnS and Si-CdSe nano-heterostructures. [27][28][29][30][31][32][33][34] In XEOL, one monitors the intensity of the luminescent bands as the X-ray energy is raised above the core level binding energy of a particular element in the system, thereby exciting an electron from a core level to a previously unoccupied state in the conduction band. The decay of the excited state can give rise to more intense luminescence via energy transfer to the optical channel.…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, it was shown that amorphous GaO x shell over crystalline Ga 2 O 3 nanowire is responsible both for "red" luminescence in the 1.7-1.8 eV range, 28 and for UV luminescence in the 3-4 eV range. To confirm our hypothesis, we measure PL spectrum of GaA nanowire using UV (3.81 eV) laser excitation.…”
Section: Figmentioning
confidence: 99%