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Uv 3101pc scanning spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The UV-3101PC is a scanning spectrophotometer manufactured by Shimadzu. It is designed to measure the absorbance or transmittance of a sample across a range of ultraviolet and visible wavelengths.

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7 protocols using uv 3101pc scanning spectrophotometer

1

Synthesis and Characterization of NaCu0.2Fe0.3Mn0.5O2

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The NaCu0.2Fe0.3Mn0.5O2 compound was synthesized using a solid-state reaction. The precursors, of Na2CO3 (99%), CuO (99%), Fe2O3 (99%) and Mn2O3 (99%) were obtained from Sigma-Aldrich, and were mixed in proportional ratios. The obtained powder was burned at 500 °C for 16 h, and then, the sample was ground, pressed into pellets and transferred to an oven at 850 °C for 24 h.
To determine the purity of the sample, powder XRD was performed using a Bruker D8 Discover with Twin/Twin optics, at room temperature, with Cu Kα radiation (λ = 1.5406 Å, 10° ≤ 2θ ≤ 80°). To precisely determine the optical properties of the prepared sample, a Shimadzu UV-3101 PC scanning spectrophotometer was used at room temperature, with a wavelength range of 200–800 nm, with a sample pellet of 0.5 mm of diameter. Finally, the electrical property measurements were obtained using complex impedance spectroscopy with a Solartron SI 1260 impedance/gain phase analyzer in the temperature and frequency ranges of 333–453 K and 10−1 to 106 Hz, respectively, with a sample pellet with a thickness of 1 mm and a diameter of 8 mm.
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2

Characterization of CdS QDs/CuO IOPCs

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The morphology of the samples was inspected using a JEOL JSM-7500F field emission scanning electron microscope (SEM) (Japan) and a JEM-2010 transmission electron microscope (TEM) (Japan) under a working voltage of 200 kV. The high-resolution TEM (HRTEM) images and EDX patterns were measured on a JEOL-2100F high-resolution transmission electron microscope (Japan) with a working voltage of 200 kV. X-ray diffraction (XRD) patterns were conducted on a RigakuD/max 2550 X-ray diffractometer. Electrochemical measurements were performed on a model CHI630D electrochemical analyzer (ChenHua Instruments Co.Ltd., Shanghai, China). Ultraviolet-visible (UV-vis) absorption spectra were measured with a Shimadzu UV-3101PC scanning spectrophotometer. The electrochemical measurements were carried out using a three-electrode system, which employed a platinum wire as the counter electrode, a saturated calomel electrode (SCE) as the reference electrode, and CdS QDs modified CuO IOPCs FTO electrodes as the working electrode.
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3

Quantification of Iron-Sulfur Proteins

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Protein concentrations were determined by the DC protein assay (Bio Rad) using bovine serum albumin as a standard. Iron concentrations were determined colorimetrically with bathophenanthroline under reducing conditions after digesting proteins with KMnO4/HCl, as described by Fish [31 (link)]. A series of dilutions of a 1000 ppm atomic absorption iron standard were used to construct a standard curve.
UV–Visible absorption spectra were recorded using septum-sealed quartz cuvettes of 1 mm or 1 cm pathlength at room temperature using a Shimadzu UV-3101 PC scanning spectrophotometer. Circular dichroism (CD) spectra were recorded with the same cuvettes using a JASCO J-715 spectropolarimeter (Jasco, Easton, MD, USA). For low temperature resonance Raman spectra, samples were concentrated to ~2 mM in [2Fe–2S] clusters and frozen as droplets on an O-ring-sealed gold-plated copper sample holder [32 (link)] mounted to the cold finger of a Displex Model CSA-202E closed cycle refrigerator (Air Products, Allentown, PA) at 17 K. Resonance Raman spectra were acquired using a Ramanor U1000 spectrometer (Instruments SA, Edison, NJ) coupled with a Sabre argon-ion laser (Coherent, Santa Clara, CA, USA). The spectroscopic data presented in this work are representative of a single experiment, but have been repeated at least three times with the same results.
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4

Annealing Effects on Ag Nanoparticles

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A 6-nm Ag layer was initially deposited on c-plane sapphire by electron beam evaporation at a deposition rate of 0.2 nm/s and a pressure of 5   10−4 Pa, and was subsequently annealed in N2 atmosphere at 300 °C, 500 °C, 600 °C and 800 °C for 5 min. SiO2 layers were fabricated by plasma-enhanced chemical vapour deposition (PECVD). For some samples, we grew SiO2 with various thicknesses beneath the Ag NPs, while for other samples, SiO2 was grown both beneath and on top of the Ag NPs to form a sandwiched Ag structure. The SiO2 thickness varies from 0 nm to 20 nm.
The morphologies of the Ag NPs and the SiO2 cladding layers were measured by SEM. The optical extinction spectra for all samples were measured using a Shimadzu UV-3101PC scanning spectrophotometer.
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5

ZnO/Carbon Nanodot Hybrid Films for UV Photodetectors

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To prepare ZnO/carbon nanodot hybrid films, the ZnO QDs and carbon nanodots solution were mixed in a series of volume ratio (1:0, 4:1, 2:1, 1:1), and the mixed solution was spun onto c-plane sapphire and then the samples were annealed at 400°C for one hour, and then at 600°C for another hour. In this way, ZnO QD and carbon nanodot hybrid films have been prepared. To fabricate UV photodetectors from the hybrid films, a thin Au layer was deposited onto the hybrid films in a vacuum evaporation method acting as contact, and interdigital electrodes were configured via a photolithography and wet etching process. For comparison, ZnO layers without the carbon nanodots have also been prepared, and photodetectors have been fabricated from the ZnO layers. The morphology of the QDs was characterized using a Philips TF-F20 transmission electron microscope operating at 200 kV. The absorption spectra of the ZnO QDs and carbon nanodots were studied in a Shimadzu UV-3101 PC scanning spectrophotometer. The photoluminescence spectra of the carbon nanodots and ZnO QDs are measured in a Shimadzu F4500 spectrometer with a Xe lamp as the excitation source. Photoresponse properties of the hybrid films were measured in a SPEX scanning monochromator employing a 150 W Xe lamp as the illumination source. The current- voltage measurement of the photodetector was measured in a Lakeshore 7707 Hall system.
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6

Characterization of Nanoparticles: A Comprehensive Approach

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As prepared NP were characterized by using UV-Vis spectrometry UV-3101PC scanning spectrophotometer (Shimadzu, Japan) with a 1 cm quartz cell. The morphology and particle size of nanoparticle was analyzed by high-resolution transmission electron microscopy (HR-TEM, Tecnai G20, FEI, USA) under an accelerating voltage of 200 kV. The samples were prepared by placing a drop on the surface of 400-mesh carbon-coated Cu grid and dried under sodium lamp for ten min before examining. X-ray diffraction (XRD) was performed to verify the NP crystalline structure and presence of facet planes (Panalytical Xpert-PRO 3050/60). Samples were prepared by concentrating TSNP solution through centrifugation at 15 000 rpm for 12 min. The supernatant was removed from the sample. The process was repeated three times. Next, concentrated solution was added dropwise on the glass slide and allowed to dry at room temperature.
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7

UV-Vis Powder Spectroscopy at Room Temp

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UV-vis powder spectroscopy was performed at room temperature using a Shimadzu UV-3101PC scanning spectrophotometer within a wavelength range of 200 to 800 nm. The equipment can measure absorbance and reflection using spherical integration and xenon light.
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