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Ts1500

Manufactured by Linkam
Sourced in United Kingdom

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.

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19 protocols using ts1500

1

Monolayer WS2 Characterization by Raman

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Monolayer WS2 sample studied here was grown on gold foil substrates by CVD, and then transferred onto a quartz substrate. The details of the synthesis and crystal-quality characterization of monolayer WS2 can be found in ref. 27 (link). Large area high-quality monolayer WS2 could be grown by this CVD method on gold foils. Single crystal monolayer WS2 is triangular, and has a size over 100 μm.
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.
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2

Alkali Fusion for Silicon Analysis

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Solidified melt sample attached to the alumina rod was digested by an alkali fusion method to prepare solution for analysis. A mixture of Na2CO3 (Sinopharm Chemical Reagent, > 99.8 pct) and H3BO3 (Sinopharm Chemical Reagent, > 99.8 pct) with a mass ratio of 3:1 was used as an alkali flux. Melt sample (about 0.15 g) and alkali flux (about 0.30 g) were mixed evenly in a Pt crucible, which was heated to 1273 K (1000 °C) at a rate of 4 K min−1 and kept for up to 40 minutes in air before cooling to room temperature at a rate of 5 K min−1. Afterward, the Pt crucible was set in a polytetrafluoroethylene (PTFE) beaker containing 100 mL of 5 pct HNO3 at 373 K (100 °C) for 2 hours to completely dissolve the substances inside. Si concentration was measured by inductively coupled plasma mass spectrometer (ICP-MS, ThermoFisher, iCAP RQ).
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.
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3

Raman Spectra of BNNT Microfibrils

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For Raman spectra measurements, the BNNT microfibril was placed on a flat quartz substrate within a programmable temperature controlled stage (Linkam TS 1500), in which the BNNTs sample temperature can be controlled in a range from room temperature (about 25 °C) to 1500 °C. The Raman spectra were obtained using Renishaw InVia Confocal Raman microscope with a 785 nm wavelength excitation laser and a nominal power of 300 mW. The samples were heated stepwise up to 1100 °C in air at a rate of 15 °C/min and held 10 minutes for every 50 °C mark to stabilize the temperature of the sample. In order to prevent/minimize laser heating induced sample damage or additional Raman shift, line scans of laser beams were used to illuminate the sample, instead of focusing laser beams on any particular spots.
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4

Brillouin Scattering of Pseudo-Cubic NBT-BT

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The crystal plate was inserted in a compact temperature controller (THMSE600 or TS1500, Linkam, Tadworth, UK) which was put under a modified microscope (BX-41, Olympus, Tokyo, Japan) for backscattering measurements. The Brillouin scattering spectrum was measured by using a conventional tandem six-pass Fabry-Perot interferometer (TFP-1 or TFP-2, JRS Co., Zürich, Switzerland) and a diode-pumped solid state laser (Excelsior 532-300, Spectra Physics, Santa Clara, CA, USA). The wavelength of the laser was 532 nm, operated at the power of tens of mW. The unpoled NBT-5%BT is pseudo-cubic without any measurable birefringence. The polarization direction of the incident laser beam was along the pseudo-cubic [100] direction. The free spectral range of the interferometer was set to 75 GHz for probing the acoustic modes. A conventional photon-counting system combined with a multichannel analyzer (1024 channels) was used to detect and average the signal. All the Brillouin spectra were measured with increasing temperature. The details of the experimental setup can be found elsewhere [39 (link),40 (link)].
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5

High-Temperature Raman Spectroscopy of Ba2NaMoO5.5

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High-temperature Raman spectra were recorded
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.
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6

Laser Annealing of Low-Doped 4H-SiC Wafers

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4H-SiC wafers with low doping (n=2.2 × 1018 cm−3) and chemical mechanical polishing were purchased from Cree. Specimens, 5 × 6 mm2, were cut from the wafers and cleaned by sequential ultrasonic baths in acetone, isopropyl alcohol and deionized water to remove grease. After cleaning, a SiC substrate was placed into a heating stage (Linkam, TS1500). This is a small chamber (100 × 100 mm2) that enables the bottom of the substrate to be heated up to 1,000 °C with inert gas supply. The sample was annealed at 650 °C for surface cleaning and it was maintained at the same temperature during laser irradiation in an Ar flow. The laser system used is comprised of a XeCl excimer laser (Coherent, LPX model, λ=308 nm, pulse duration ∼30 ns) and beam delivery optics with a homogenizer optical system. The laser beam is concentrated 5 × by a projection lens through a square pattern mask. Each pulse had a laser fluence of 1,653 mJ cm−2 and a repetition rate of 1 Hz. For multi-pulse irradiations over 100 pulses, 5 Hz was used to reduce the processing time. Both repetition rates appeared to have the same effect because the heating and cooling produced by the nanosecond pulse are completed within a microsecond. All the laser experiments were performed with the same substrate and experimental conditions except for the number of pulses.
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7

In Situ MW Hydrothermal Thermal Analysis

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To determine the temperature profile during the in situ MW hydrothermal experiment, temperature-resolved heating experiments for the empty PTFE tube was performed to determine the thermal expansion coefficient. A Linkam TS 1500 furnace was deployed to heat the empty PTFE tube from 33° to 233°C in a heating rate of 5°C min−1. The XRD patterns were simultaneously recorded during the heating process.
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.
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8

Solid-State Synthesis of Layered Ni-Mn-Co Oxide

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The precursor Ni1/3Mn1/3Co1/3(OH)2 was completely mixed with LiOH in a molar ratio of 1:1.05 by grinding for 1 hour. For temperature-resolved XRD measurements, the mixture was pressed into pellets with a thickness of around 1 mm and a diameter of 7 mm and then placed in a furnace (Linkam TS 1500) vertically, with the window perpendicular to the x-ray beam. The pellets were then heated to 850°C in air with a rate of 20°C min−1. High-energy XRD patterns were collected at Sector 28-ID-2 of the NSLS-II. The wavelength of the x-ray beam was 0.23696 Å.
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.
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9

Annealing Emitter Structures under Vacuum

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Emitter structures were annealed in a high-temperature heating stage (Linkam, TS1500) at 2 × 10−2 mbar vacuum pressure using a rough vacuum pump, and in a high-temperature vacuum furnace (RD-G WEBB) at 2 × 10−6 mbar vacuum pressure. The temperature was ramped at a rate of 10 °C min−1. O2 concentration in the encapsulated area is measured using an O2 sensor (Sensor type: SO-B0-010, in the range up to 2000 ppm, purchased from SENSORE Electronic GmbH) and it is assembled on a generic sensor board. Ar gas (99.999% from Linde) at a pressure of 3 bar is used to encapsulate the annealing chamber.
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10

Determination of Temperature Dependence of SiV Luminescence

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The developed DHT was placed in an air environment for a preliminary determination of the power density of optical excitation at a wavelength that did not lead to a shift of the zero-phonon SiV luminescence line, and, consequently, to heating. The measured power density was used to determine the temperature dependence of the spectral position of the zero-phonon line center in a Linkam TS1500 thermostat, stabilized at a predetermined level with an accuracy of ~ 1 °C. The temperature in the chamber was changed in increments of 10 °C. At each step, the SiV luminescence spectrum was recorded and the spectral position of the zero-phonon line maximum was determined according to the algorithm proposed in our previous work1 (link).
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