Luisa Spallino

Luminescence from nearly isolated surface defects in silica nanoparticles

A structured emission/excitation pattern, proper of isolated defects, arises in a vacuum from silica nanoparticles. The luminescence, centered around 3.0-3.5 eV, is characterised by a vibronic progression due to the phonon coupling with two localised modes of frequency  ∼1370 cm(-1) and  ∼360 cm(-1), and decays in about 300 ns at 10 K. On increasing the temperature, the intensity and the lifetime decrease due to the activation of a non-radiative rate from the excited state. Concurrently, the temperature dependence of the lineshape evidences the low coupling with non-localised modes of the matrix (Huang-Rhys factor S ~ 0.2) and the poor influence of the inhomogeneous broadening. These findings outline an uncommon behaviour in the field of the optical properties of defects in amorphous solids, evidencing that the silica surface can allocate luminescent defects almost disentangled from the basal network.

Insight into the defect–molecule interaction through the molecular-like photoluminescence of SiO2 nanoparticles

Luminescence properties due to surface defects in SiO2 are the main keystone with particles that have nanoscale dimensions, thus motivating their investigation for many emission related applications in the last few decades. A critical issue is the role played by the atmosphere that, by quenching mechanisms, weakens both the efficiency and stability of the defects. A deep knowledge of these factors is mandatory in order to properly limit any detrimental effects and, ultimately, to offer new advantageous possibilities for their exploitation. Up to now, quenching effects have been interpreted as general defect conversion processes due to the difficulty in disentangling the emission kinetics by the action of the specific quenchers. To overcome this limit, we report a time-resolved investigation of the effects induced in specific controlled molecular environments (N2, O2, CO2 and H2O) on the exceptional molecular-like luminescence that is observed around 3.0–3.4 eV in SiO2 nanoparticles. A comparison with the effects under vacuum indicates changes of the luminescence intensity and lifetime that agree with two quenching mechanisms, static and dynamic. The peculiarity of the spectral features, together with a powerful investigation approach, makes this the system of choice to probe inside the dynamics of the molecule–defect interactions and to reveal promising characteristics for molecular-sensing purposes.

Vibronic structures in the visible luminescence of silica nanoparticles

Time resolved photoluminescence investigation in air and in vacuum atmosphere of the visible luminescence related to silica surface defects is here reported. Two contributions can be singled out: one, observed both in air and in vacuum, is the well-known blue band, peaked around 2.8 eV decaying in ∼5 ns; the other, only observed in vacuum, is a structured emission in the violet range characterized by two vibronic progressions spaced 1370 cm−1 and 360 cm−1 decaying in ∼100 ns. In contrast with previous attribution, the well distinguishable spectroscopic properties together with the observation of the effects induced by the interaction with nitrogen allow to state that the emission bands originate by two different defects.