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Isr 2600plus integrating sphere attachment

Manufactured by Shimadzu
Sourced in Japan

The ISR-2600Plus Integrating Sphere Attachment is a laboratory equipment designed to measure the diffuse reflectance and transmittance of solid, liquid, and powder samples. It is compatible with Shimadzu's UV-2600 and UV-2700 spectrophotometers, providing a standardized method for optical property measurements.

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3 protocols using isr 2600plus integrating sphere attachment

1

Comprehensive Characterization of BYW Samples

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The X-ray powder diffraction (XRPD) patterns of all BYW samples were collected by using a Rigaku SmartLab X-ray diffractometer in Bragg–Brentano geometry with Cu Kα radiation. The diffracted beam was monochromatized by silicon single crystals and collected by using a D/tex linear detector. The XRPD data were collected over a 2θ range of 10° to 120° with a step size of 0.02°.
High-resolution electron microscopy images were obtained using a Zeiss Ultra Plus High Resolution Field Emission Gun Scanning Electron Microscope (FEGSEM). Energy-dispersive X-ray spectroscopy (EDS) spectra were acquired using an Oxford X-MaxN Silicon drift detector (SDD). The diffuse reflectance spectra of the powders were recorded using a Shimadzu UV 2600 spectrophotometer equipped with an ISR-2600Plus Integrating Sphere Attachment. The Raman spectra were collected using a micro-Raman spectrometer (iHR550, Horiba) with a green laser (λ = 514 nm).
Diffuse reflectance measurements were performed by putting a small amount of sample (50 mg) on top of a BaSO4 tablet and then pressing. Pure BaSO4 was used as a baseline because its reflectance is close to 100% in the examined range (200 nm < λ < 700 nm).
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2

Spectroscopic Characterization of Films

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UV-visible absorption spectra were measured on a Shimadzu 2600 spectrophotometer with an ISR-2600Plus Integrating Sphere Attachment, so that the transmittance (T) and the reflectance (R) of the films could be measured. The absorbance of the samples was calculated from −log10 T, while the absorptance was calculated from 1-T-R. Fluorescence spectra were measured with a Horiba Jobin Yvon Fluorolog-2 fluorometer.
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3

Synthesis and Characterization of Iron Titanate Nanoparticles

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Iron titanate nanoparticle synthesis was conducted following a modified sol-gel method (Vasiljevic et al. 2020a) . Iron(III) nonahydrate, titanium isopropoxide, oxalic acid (chelating agent) and citric acid (surfactant) were mixed on a magnetic mixer maintaining the temperature between 80 and 90 • C until a gel was formed. The formed gel was heated to 300 • C until a powder formed, and then calcined in a chamber furnace at 750 • C for 3 h. Structural characteristics of the obtained powder were investigated by measuring X-ray diffraction (range 2θ = 10-90 • , step 0.05 s, acquisition rate 1 • /min, Rigaku Ultima IV diffractometer, Tokyo, Japan) and FT-IR spectrum (range 400-4000 cm -1 , FT-IR Nicolet 6700 ATR device, Waltham, MA, USA). The optical band gap was determined by measuring and analysing UV-Vis diffuse reflectance spectrum (Shimadzu UV-2600 with an ISR2600 Plus integrating sphere attachment, Kyoto, Japan). The powder morphology was investigated by Field emission electron microscopy -FESEM (TESCAN MIRA3 XM, Brno, Czech Republic) and transmission electron microscopy -TEM (JEM-2100 200 kV, JEOL Ltd. Tokyo, Japan). The specific surface area and pore structure were determined from measured N 2 adsorption-desorption isotherms (Micromeritics ASAP 2020, Norcross, GA, USA). Prior to measurement, the powder sample was degassed at 150 • C for 10 h under reduced pressure.
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