2003
DOI: 10.1016/j.msec.2003.09.077
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Mesoporous silica photoluminescence properties in samples with different pore size

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Cited by 11 publications
(14 citation statements)
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“…The time-dependent PL decay is not described by a single decay lifetime (that is, it does not follow a single-exponential decay function) while good fitting is obtained with a double-exponential function, as in the case of other TRPL experiments on mesoporous SiO 2 . [22] Fitting the data by means of a double-exponential function I(t) ¼ A 1 exp(Àt/t 1 ) þ A 2 exp(Àt/t 2 ), decay lifetimes of the order of 1 and 10 ns respectively are obtained, similarly to findings reported for sol-gel synthesized mesoporous silica samples. [23] By changing the concentrations of NO 2 in the test chamber, no significant variations in the recombination dynamics were observed, as the PL lifetimes were found to be unaffected by the presence of nitrogen dioxide in the range from 1 to 50 ppm.…”
Section: Full Papersupporting
confidence: 75%
See 1 more Smart Citation
“…The time-dependent PL decay is not described by a single decay lifetime (that is, it does not follow a single-exponential decay function) while good fitting is obtained with a double-exponential function, as in the case of other TRPL experiments on mesoporous SiO 2 . [22] Fitting the data by means of a double-exponential function I(t) ¼ A 1 exp(Àt/t 1 ) þ A 2 exp(Àt/t 2 ), decay lifetimes of the order of 1 and 10 ns respectively are obtained, similarly to findings reported for sol-gel synthesized mesoporous silica samples. [23] By changing the concentrations of NO 2 in the test chamber, no significant variations in the recombination dynamics were observed, as the PL lifetimes were found to be unaffected by the presence of nitrogen dioxide in the range from 1 to 50 ppm.…”
Section: Full Papersupporting
confidence: 75%
“…The violet emission is predominantly observed in fresh stoichiometric a-SiO 2 films and in mesoporous silica samples prepared by sol-gel synthesis. [22,25] It is believed to originate from surface centers [22,23,25,26] and is due to the fact that it can be significantly quenched (or even totally disappear) when the sample surface releases H 2 and H 2 O [24] (which may occur, for instance, during annealing at high temperatures); it has been correlated to the presence of Si-OH bonds, although a precise attribution to specific centers has not been established definitely. In our case (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, Anedda et al . demonstrated that the spectral distribution of the PL signal depends on the pore diameter, which was attributed to changes in the bonding energies by the interaction in close proximity of the Si–OH and O–H groups, reinforcing their electrostatic interaction and consequently affecting their electronic levels at higher or lower energies, in particular, in the green region of the spectrum, which may explain the enhancement of this region emission observed in Figure .…”
Section: Discussionmentioning
confidence: 91%
“…However, in Anedda et al . 's work , the broad emission results because their porous material showed a non‐uniform broad distribution of pore diameters; thus, the final featureless broad curve, or at most composed of two broad emission PL curves, results from the envelope for all pores which forms a continuous distribution in pore diameter.…”
Section: Discussionmentioning
confidence: 93%
“…[30,33,37] In the last years our endeavor has been dedicated to the characterization of the optical features of mesoporous silica, an ideal benchmark of nanostructured silica with very large specific surface area, up to 600 m 2 /gr in the investigated samples, and skeleton walls in the nanometer range. [17,26,27,34,35,[45][46][47][48][49][50][51] The emission properties in the UV and blue range have been investigated as a function of the pore diameter, by considering the hydrophilic character of the silica surface, [17,46] and as a function of different environment conditions, by analyzing the effects of long air exposure, [51] vacuum treatment, [49] oxygen or nitrogen purging and interaction with strongly oxidizing polar solvent (H 2 O 2 ). [34,35] In the present work we collect all the results gathered in our research, including some new experiments with protic and aprotic solvents, and discuss them in the framework of the proposed models.…”
Section: Introductionmentioning
confidence: 99%