We have demonstrated temperature-independent optical transitions from thermally diffused Gd in GaN. The emission wavelength is sub-bandgap with respect to GaN. The origin of photon generation is identified as atomic transitions in Gd hosted in the weak interaction field of GaN. The emission linewidth remains sub-nanometer (0.1-0.6 nm) from 19 to 300 K for all the optical pumping intensities. The shift in wavelength with temperature and optical pumping is negligible (∼0.8 nm) for the entire temperature window. The output intensity is found to scale linearly with the pumping power. The magnetic, electrical, and physical characterizations indicate that Gd acts as an electron trap in GaN. Transient absorption spectroscopy discovers a major nonradiative parallel path for carrier leaking. The observed characteristics may find potential applications in narrow linewidth optical sources.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1364/OL.42.002161 | DOI Listing |
ACS Appl Mater Interfaces
November 2024
Institute of Low Temperature and Structure Research, Polish Academy of Sciences, Okolna 2, 50-422 Wroclaw, Poland.
Luminescent manometry has gained significant popularity in recent years due to its capability to provide in situ pressure measurements in a remote manner. Therefore, there is a growing need to identify phosphors with pressure-dependent spectroscopic properties that can be utilized to develop highly sensitive pressure sensors operating over a wide pressure range. Hence, we present a novel temperature-invariant luminescent manometer based on Cr ion emission in pyroxene CaSrMgSiO:Cr.
View Article and Find Full Text PDFInorg Chem
October 2024
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland.
We present a synergistic experimental-theoretical methodology for the investigation of lanthanide-based single-molecule magnets (SMMs), demonstrated using the example of novel heterometallic molecules incorporating Nd/Ce ions combined with three different, rarely explored, pentacyanidocobaltate(III) metalloligands, [Co(CN)(azido/nitrito-/iodido)]. The theoretical part of our approach broadens the exploration of calculations for lanthanide(III) complexes toward the convenient simulations of such physical characteristics as directional dependences of Helmholtz energy, magnetization, susceptibility, and their thermal and field evolution, as well as light absorption and emission bands. This work was conducted using newly designed SlothPy software (https://slothpy.
View Article and Find Full Text PDFMol Ther Oncol
September 2024
Scuola Normale Superiore, Laboratorio NEST, Piazza San Silvestro 12, 56127 Pisa, Italy.
The successful trajectory of liposome-encapsulated doxorubicin (e.g., Doxil, which has been approved by the U.
View Article and Find Full Text PDFJ Chem Phys
July 2024
The Institute of Optics, University of Rochester, Rochester, New York 14627, USA.
The generation of exciton-polaritons through strong light-matter interactions represents an emerging platform for exploring quantum phenomena. A significant challenge in colloidal nanocrystal-based polaritonic systems is the ability to operate at room temperature with high fidelity. Here, we demonstrate the generation of room-temperature exciton-polaritons through the coupling of CdSe nanoplatelets (NPLs) with a Fabry-Pérot optical cavity, leading to a Rabi splitting of 74.
View Article and Find Full Text PDFHeliyon
April 2024
Department of Physics, Sungkyunkwan University, Suwon, Gyeonggi-do, 16419, Republic of Korea.
Planckian behavior has been recently observed in LaSrCuO at the pseudogap critical point. The Planckian behavior takes place in an intriguing quantum metallic state at a quantum critical point. Here, the Planckian behavior was simulated with an energy-independent (or flat) and weakly temperature-dependent electron-boson spectral density (EBSD) function by using a generalized Allen's (Shulga's) formula.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!