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X maxn silicon drift detector

Manufactured by Oxford Instruments
Sourced in United Kingdom

The X-MaxN silicon drift detector is a high-performance energy-dispersive X-ray (EDX) detector designed for elemental analysis in scanning electron microscopy (SEM) and other X-ray spectroscopy applications. It features a large active area and advanced electronics to provide high-resolution X-ray detection and rapid data acquisition.

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2 protocols using x maxn silicon drift detector

1

Characterization of Electrocatalyst Morphology

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The morphology and microstructure of the electrocatalysts were characterized with the aid of field emission scanning electron microscopy (FE-SEM, Tescan Lyra-3, TESCAN, Brno, Czech Republic) equipped with an energy-dispersive X-ray spectrometer (EDX, X-MaxN silicon drift detector, Oxford Instruments, Oxford, UK). Transmission and high-resolution transmission electron microscopes and selected area electron diffraction (TEM/HR-TEM, FEI Tecnai F20, FEI Europe B. V., Eindhoven, The Netherlands) (SAED) were used to further discern the microstructural attributes in more detail. Phase analysis was performed using X-ray diffractometry (XRD, Rigaku MiniFlex, Rigaku Co., Tokyo, Japan), and the diffractometer was operated at a 0.15416 nm wavelength, 10 mA current, and 30 kV voltage. XRD patterns were recorded from 5 to 80° in a 2θ range with 0.02° steps. The elemental state was analyzed using X-ray photoelectron spectroscopy (XPS, Thermo Scientific ESCALAB 250Xi, Waltham, MA, USA). N2 adsorption–desorption isotherms were collected at 77.35 K using Quantachrome Instruments (Boynton Beach, FL, USA).
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2

Characterization of Spherical AuNPs by TEM

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Three microliters of AuNP solution were deposited onto freshly glow discharged 200 mesh nickel TEM grids coated with a carbon-stabilized formvar film (Electron Microscopy Sciences, Hatfield, USA). The AuNPs adsorbed onto the film surface for 5 min after which the excess solution was wicked away using filter paper. The grids were then washed in quick succession in three droplets of MilliQ water. Excess water was removed using filter paper and the grids allowed to air dry.
TEM was performed utilizing a FEI Tecnai T20 G2 (Thermo Fisher Scientific, Waltham, USA) operating at 200 kV located at the Center for Electron Nanoscopy at DTU. Both low and high magnification images, as well as energy dispersive X-ray spectra (EDS), were acquired for each AuNP sample. Images were acquired using a CCD camera equipped with Digital Micrograph (Gatan, Pleasanton, USA), and EDS spectra were acquired using a X-maxN Silicon Drift Detector (Oxford Instruments, Abingdon, UK). Image analysis was performed using Fiji analysis software 69 (link). Nanoparticle diameter was determined using the 'analyze particle function' of Fiji to obtain an area for each nanoparticle, making sure not to include nanoparticles that were overlapping in the measurements, and converting this value to a diameter assuming a spherical nanoparticle. A minimum of 250 nanoparticles were measured for each sample.
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