2 research outputs found
Silicon Quantum Dots in Dielectric Scattering Media: Broadband Enhancement of Effective Absorption Cross Section by Light Trapping
We
report strong enhancements of the effective absorption cross section
and photoluminescence (PL) intensity of silicon quantum dots (Si QDs)
with 2.8–6.8 nm in diameter in a highly scattering dielectric
medium. The scattering medium is a polymer thin film with submicrometer
size pores inside, supporting the resonant cavity modes in the visible
range. By the scattering associated with the cavity modes, efficient
light trapping into a polymer film with ∼1 μm in thickness
is achieved, which leads to 30–40 times enhancement of the
effective absorption cross section of embedded Si QDs in a green–red
wavelength range. The scattering medium can also enhance up to 40
times the PL of QDs. Detailed analysis reveals that the enhancements
of the extraction efficiency as well as the excitation efficiency
contribute to the PL enhancement
Overpotential-Induced Introduction of Oxygen Vacancy in La<sub>0.67</sub>Sr<sub>0.33</sub>MnO<sub>3</sub> Surface and Its Impact on Oxygen Reduction Reaction Catalytic Activity in Alkaline Solution
Oxygen reduction reaction (ORR) catalytic
activity of La<sub>0.67</sub>Sr<sub>0.33</sub>MnO<sub>3</sub> epitaxial
thin films was investigated
in a KOH solution by using a rotating-disk electrode. We found that
while the films exhibit ORR current, the current is not limited by
oxygen transport resulting from the film electrode rotation and shows
the large hysteresis against the potential sweep direction. This behavior
is in stark contrast to the oxygen reduction reaction activity of
an electrode ink made from LSMO bulk powder, whose ORR current is
oxygen-transport limited. <i>In situ</i> synchrotron X-ray
absorption spectroscopy also reveals that the valence state of Mn
in the LSMO film surface is lowered under the reducing atmosphere
caused by the overpotential. This indicates the overpotential-induced
introduction of oxygen vacancies in the film surface. We also show
that the ORR current of the LSMO films exposed to the reducing atmosphere
is lowered than that of the original surface. These results indicate
that the ORR catalytic activity of LSMO surfaces is strongly influenced
by oxygen vacancies