3 research outputs found
Generalized Brewster-Kerker effect in dielectric metasurfaces
Polarization is one of the key properties defining the state of light. It was
discovered in the early 19th century by Brewster, among others, while studying
light reflected from materials at different angles. These studies led to the
first polarizers, based on Brewster's effect. One of the most active trends in
photonics now is devoted to the study of miniaturized, sub-wavelength devices
exhibiting similar, or even improved, functionalities compared to those
achieved with bulk optical elements. In the present work, it is theoretically
predicted that a properly designed all-dielectric metasurface exhibits a
generalized Brewster effect potentially for any angle, wavelength and
polarization of choice. The effect is experimentally demonstrated for an array
of silicon nanodisks at visible wavelengths. The underlying physics of this
effect can be understood in terms of the suppressed scattering at certain
angles that results from the interference between the electric and magnetic
dipole resonances excited in the nanoparticles, predicted by Kerker in early
80s. This reveals deep connection of Kerker's and Brewster's legacies and opens
doors for Brewster phenomenon to new applications in photonics, which are not
bonded to a specific polarization or angle of incidence.Comment: 12 pages, 5 figures, and supplementary information (22 pages
Generic Heterogeneously Integrated III–V Lasers-on-Chip With Metal-Coated Etched-Mirror
Empagliflozin in Patients with Chronic Kidney Disease
Background The effects of empagliflozin in patients with chronic kidney disease who are at risk for disease progression are not well understood. The EMPA-KIDNEY trial was designed to assess the effects of treatment with empagliflozin in a broad range of such patients. Methods We enrolled patients with chronic kidney disease who had an estimated glomerular filtration rate (eGFR) of at least 20 but less than 45 ml per minute per 1.73 m(2) of body-surface area, or who had an eGFR of at least 45 but less than 90 ml per minute per 1.73 m(2) with a urinary albumin-to-creatinine ratio (with albumin measured in milligrams and creatinine measured in grams) of at least 200. Patients were randomly assigned to receive empagliflozin (10 mg once daily) or matching placebo. The primary outcome was a composite of progression of kidney disease (defined as end-stage kidney disease, a sustained decrease in eGFR to < 10 ml per minute per 1.73 m(2), a sustained decrease in eGFR of & GE;40% from baseline, or death from renal causes) or death from cardiovascular causes. Results A total of 6609 patients underwent randomization. During a median of 2.0 years of follow-up, progression of kidney disease or death from cardiovascular causes occurred in 432 of 3304 patients (13.1%) in the empagliflozin group and in 558 of 3305 patients (16.9%) in the placebo group (hazard ratio, 0.72; 95% confidence interval [CI], 0.64 to 0.82; P < 0.001). Results were consistent among patients with or without diabetes and across subgroups defined according to eGFR ranges. The rate of hospitalization from any cause was lower in the empagliflozin group than in the placebo group (hazard ratio, 0.86; 95% CI, 0.78 to 0.95; P=0.003), but there were no significant between-group differences with respect to the composite outcome of hospitalization for heart failure or death from cardiovascular causes (which occurred in 4.0% in the empagliflozin group and 4.6% in the placebo group) or death from any cause (in 4.5% and 5.1%, respectively). The rates of serious adverse events were similar in the two groups. Conclusions Among a wide range of patients with chronic kidney disease who were at risk for disease progression, empagliflozin therapy led to a lower risk of progression of kidney disease or death from cardiovascular causes than placebo