The micro-Raman system used in this study is Renishaw inVia with a Linkam TS1500 heating system. Renishaw inVia Micro-Raman system has a spectral resolution smaller than 1 cm−1 and a 50 × long working-distance lens which can focus laser beam to a spot less than 1 μm in diameter. A 514.5 nm laser is used. The power incident on the sample is 1.97 mW, low enough to avoid heating of the sample. The Linkam TS1500 heating system has a temperature control accuracy of 1 °C, heating the sample with a step of 10 °C at a rate of 10 °C/min. To stabilize the sample temperature, ten minutes’ delay is applied at each temperature step till a Raman spectrum is taken, ensuring sufficient time to reach thermal equilibrium.
Ts1500
The TS1500 is a temperature stage designed for use with optical microscopes. It provides a controlled thermal environment for samples during microscopic observation and analysis.
Lab products found in correlation
19 protocols using ts1500
Monolayer WS2 Characterization by Raman
The micro-Raman system used in this study is Renishaw inVia with a Linkam TS1500 heating system. Renishaw inVia Micro-Raman system has a spectral resolution smaller than 1 cm−1 and a 50 × long working-distance lens which can focus laser beam to a spot less than 1 μm in diameter. A 514.5 nm laser is used. The power incident on the sample is 1.97 mW, low enough to avoid heating of the sample. The Linkam TS1500 heating system has a temperature control accuracy of 1 °C, heating the sample with a step of 10 °C at a rate of 10 °C/min. To stabilize the sample temperature, ten minutes’ delay is applied at each temperature step till a Raman spectrum is taken, ensuring sufficient time to reach thermal equilibrium.
Alkali Fusion for Silicon Analysis
In some cases, solidified melt sample was rinsed by distilled water, followed by filtration to recover insoluble residues. These residues after drying at 353 K (80 °C) for 24 hours were characterized by Powder X-ray diffractometer (PXRD, CuKα, Bruker, D8 Advance). In-situ Raman spectroscopy to evaluate the structure of Si(IV) anions was conducted by a spectrometer (WITec, Alpha300R) with a high-temperature stage (Linkam, TS1500) heated in a flowing Ar atmosphere.
Raman Spectra of BNNT Microfibrils
Brillouin Scattering of Pseudo-Cubic NBT-BT
High-Temperature Raman Spectroscopy of Ba2NaMoO5.5
using a Horiba Jobin-Yvon
Aramis spectrometer equipped with a Linkam TS-1500 heating device.
The Ba2NaMoO5.5 sample was placed in a platinum
crucible and inserted in the furnace. A rate of 10 K min−1 was applied upon heating, and 5 min of stabilization time was maintained
at each temperature plateau before acquisition of the spectra. The
632.8 nm line of a He–Ne laser was used as the excitation wavelength
and focused by means of an Olympus BX41 (magnification factor of 50×),
thus delivering ∼10 mW at the sample surface. Slits and a confocal
hole were set to result in a resolution of 1 cm–1. For each spectrum, an acquisition time of 4 s was considered with
an average of four scans. Before analysis, the apparatus was calibrated
with a silicon wafer, using the first-order Si line at 520.7 cm–1. Band component analysis of the different spectra
was performed with the Jandel Peakfit software, using pseudo-Voigt
functions with the minimum number of components. Correlation coefficients
of >0.997 were systematically obtained.
Laser Annealing of Low-Doped 4H-SiC Wafers
In Situ MW Hydrothermal Thermal Analysis
To study the MW thermal effect during the in situ MW hydrothermal experiment, MW heating experiments for the empty PTFE tube, the PTFE tube with H2O, the PTFE tube with H2O and LiOH (LiOH saturated solution), and the PTFE tube with H2O (15 μl) and Ni1/3Mn1/3Co1/3(OH)2 (30 mg) were also performed using the same conditions as that during in situ MW hydrothermal synthesis. Time-resolved high-energy XRD patterns were collected at Sector 28-ID-2 of the NSLS-II. The wavelength of synchrotron x-ray beam is 0.1885 Å.
Solid-State Synthesis of Layered Ni-Mn-Co Oxide
To determine the activation energy of the phase transformation during the solid-state synthesis, solid-state reactions were also performed at three different control temperatures: 320°, 330°, and 340°C. The corresponding calibrated temperatures are 293°, 302°, and 311°C, respectively. The mixture used here was the same with that during in situ MW hydrothermal synthesis and in situ conventional hydrothermal synthesis above. Time-resolved XRD were also collected. High-energy XRD patterns were collected at Sector 28-ID-1 of the NSLS-II. The wavelength of the x-ray beam was 0.1886 Å. The temperature of the furnace is precalibrated using ceria as thermal expansion standard.
Annealing Emitter Structures under Vacuum
Determination of Temperature Dependence of SiV Luminescence
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