Hexagonal boron nitride (h-BN) is an attractive van der Waals material for studying fluorescent defects due to its large bandgap. In this work, we demonstrate enhanced pink color due to neutron irradiation and perform electron paramagnetic resonance (EPR) measurements. The new point defects are tentatively assigned to doubly-occupied nitrogen vacancies with (S = 1) and a zero-field splitting (D = 1.2 GHz). These defects are associated with a broad visible optical absorption band and near infrared photoluminescence band centered at ~ 490 nm and 820 nm, respectively. The EPR signal intensities are strongly affected by thermal treatments in temperature range between 600 to 800ºC, where also the irradiation-induced pink color is lost. Our results are important for understanding of point defects in h-BN and their deployment for quantum and integrated photonic applications.
We demonstrate that hybrid systems
of porphyrins and chirality
enriched (6,5) single-walled carbon nanotubes (E-SWCNTs) are better
candidates for photodynamic therapy (PDT) than their components alone.
Surprisingly, the E-SWCNTs act as optical absorption enhancers to
the porphyrins increasing the oxygen singlet production when illuminated
by a light source with energy higher than the E-SWCNT gap plus the
equivalent in energy of an E-SWCNT phonon. The phenomenon is explained
based on energy transfer from the E-SWCNT to the porphyrin which finally
transfers it to the oxygen molecule. The large optical absorption
cross section of E-SWCNT and the resonance of the porphyrin to the
oxygen singlet–triplet transition are responsible for the synergistic
effect.
Semiconductor
nanomembranes are promising systems for many applications,
since the band structure of a given material can be tailored to achieve
specific configurations, which are not feasible by conventional growth
procedures on rigid substrates. Here we show that optically active
III–V membranes containing InAs quantum dots exhibit a pronounced
photoluminescence enhancement with respect to equivalent systems grown
on top of flat substrates. The effect is explained by the formation
of carrier depletion regions symmetrically located with respect to
the optically active layer. This leads to the filling of excited states
of the quantum dots and the overall spectra are enhanced at higher
energies. Changes on the strain field that are expected to lead to
a red-shift of the quantum dot emission play a reduced role in the
final emission spectra in comparison with the depletion effects. These
effects can be considered as another degree of freedom and a key ingredient
for band engineering of extremely thin semiconductor membranes.
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