Designing an efficient
hybrid structure photocatalyst for photocatalytic
decomposition and hydrogen (H2) evolution has been considered
a great choice to develop renewable technologies for clean energy
production and environmental remediation. Enhanced charge transfer
(CT) based on the interaction between a noble metal and a semiconductor
is a crucial factor influencing the movement of photogenerated electron–hole
pairs. Herein, we focus on the recent advances related to plasmon-enhanced
noble metals and the semiconductor nature to drive the photocatalytic
H2 production and photodegradation of the organic dye rhodamine
B (RhB) under UV and visible light irradiation. Specifically, the
combination of concerted catalysis and green nanoengineering strategies
to design ZnO-based composite photocatalysts and their decoration
with metallic Ag have been realized by the radio frequency (RF) sputtering
technique at room temperature. This simultaneity enhances the interface
coupling between Ag and ZnO and reduces the energy threshold. The
creation of charge transfer in the heterojunction and Schottky barrier
changes the photoelectronic properties of the as-synthesized Al-doped
ZnO (AZO); afterward, these effects promote the migration, transportation,
and separation of photoinduced charge carriers and enhance the light-harvesting
efficiency. As a result, the as-synthesized AZO-20 hybrid nanostructure
exhibits a photocurrent density of 2.5 mA/cm2 vs Ag/AgCl,
which is improved by almost 12 times compared with that of bare ZnO
(0.2 mA/cm2). The hydrogen evolution rates of AZO-20 were
∼38 and ∼24 μmol/h under UV and visible light
exposure, which are almost five- and tenfold higher than those of
pristine ZnO, respectively. Additionally, the RhB degradation efficacies
of the obtained AZO-20 were greater than almost 97 and 82% under UV
and visible light illumination, respectively. The achieved apparent
rate constant for the photocatalytic RhB decomposition was 0.014 min–1, indicating that it is 14-fold than that in pristine
ZnO (0.001 min–1). Heterostructure AZO photocatalysts
possess excellent practical stability in the water-splitting reaction
and photocatalytic RhB decomposition, posing as promising candidates
in practical works for pollution and energy challenges.
We investigated the effect of single and multidopants on the thermoelectrical properties of host ZnO films. Incorporation of the single dopant Ga in the ZnO films improved the conductivity and mobility but lowered the Seebeck coefficient. Dual Ga- and In-doped ZnO thin films show slightly decreased electrical conductivity but improved Seebeck coefficient. The variation of thermoelectric properties is discussed in terms of film crystallinity, which is subject to the dopants' radius. Small amounts of In dopants with a large radius may introduce localized regions in the host film, affecting the thermoelectric properties. Consequently, a 1.5 times increase in power factor, three times reduction in thermal conductivity, and 5-fold enhancement in the figure of merit ZT have been achieved at 110 °C. The results also indicate that the balanced control of both electron and lattice thermal conductivities through dopant selection are necessary to attain low total thermal conductivity.
We demonstrated modulation of the waveguide mode mismatch via liquid cladding of the controllable refractive index for label-free quantitative detection of concentration of chemical or biological substances. A multimode optical fiber with its core exposed was used as the sensor head with the suitable chemical modification of its surface. Injected analyte liquid itself formed the liquid cladding for the waveguide. We found that modulation of the concentration of analyte injected enables a degree of the waveguide mode mismatch to be controlled, resulting in sensitive change in optical power transmission, which was utilized for its real-time quantitative assay. We applied the device to quantitating concentration of glycerol and bovine serum albumin (BSA) solutions. We obtained experimentally the limit of detection (LOD) of glycerol concentration, 0.001% (volume ratio), corresponding to the resolvable index resolution of ∼1.02 × 10 RIU (refractive index unit). The presented sensors also exhibited reasonably good reproducibility. In BSA detection, the sensor device response was sensitive to change in the refractive indices not only of liquid bulk but also of layers just above the sensing surface with higher sensitivity, providing the LOD experimentally as ∼3.7 ng/mL (mass coverage of ∼30 pg/mm). A theoretical model was also presented to invoke both mode mismatch modulation and evanescent field absorption for understanding of the transmission change, offering a theoretical background for designing the sensor head structure for a given analyte. Interestingly, the device sensing length played little role in the important sensor characteristics such as sensitivity, unlike most of the waveguide-based sensors. This unraveled the possibility of realizing a highly simple structured label-free sensor for point-of-care testing in a real-time manner via an optical waveguide with liquid cladding. This required neither metal nor dielectric coating but still produced sensitivity comparable to those of other types of label-free sensors such as plasmonic fiber ones.
The development of improved methods for the synthesis of monodisperse gold nanoparticles (Au NPs) is of high priority because they can be used as substrates for surface-enhanced Raman scattering (SERS) applications relating to biological lipids.
Antipsychotic drugs produce acute behavioral effects through antagonism of dopamine and serotonin receptors, and long-term adaptive responses that are not well understood. The goal of the study presented here was to use Caenorhabditis elegans to investigate the molecular mechanism or mechanisms that contribute to adaptive responses produced by antipsychotic drugs. First-generation antipsychotics, trifluoperazine and fluphenazine, and second-generation drugs, clozapine and olanzapine, increased the expression of tryptophan hydroxylase-1::green fluorescent protein (TPH-1::GFP) and serotonin in the ADF neurons of C. elegans. This response was absent or diminished in mutant strains lacking the transient receptor potential vanilloid channel (TRPV; osm-9) or calcium/calmodulin-dependent protein kinase II (CaMKII; unc-43). The role of calcium signaling was further implicated by the finding that a selective antagonist of calmodulin and a calcineurin inhibitor also enhanced TPH-1::GFP expression. The ADF neurons modulate foraging behavior (turns/reversals off food) through serotonin production. We found that short-term exposure to the antipsychotic drugs altered the frequency of turns/reversals off food. This response was mediated through dopamine and serotonin receptors and was abolished in serotonin-deficient mutants (tph-1) and strains lacking the SER-1 and MOD-1 serotonin receptors. Consistent with the increase in serotonin in the ADF neurons induced by the drugs, drug withdrawal after 24-hr treatment was accompanied by a rebound in the number of turns/reversals, which demonstrates behavioral adaptation in serotonergic systems. Characterization of the cellular, molecular, and behavioral adaptations to continuous exposure to antipsychotic drugs may provide insight into the long-term clinical effects of these medications.
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