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Multipak software version 9

Manufactured by Physical Electronics
Sourced in United States

MultiPak software version 9.6.015 is an analytical software tool used for the processing and visualization of spectroscopic data. The software provides functionality for data acquisition, analysis, and presentation.

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2 protocols using multipak software version 9

1

XPS Characterization of Surface-Immobilized Metal Nanoparticles

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Gold-coated silicon substrates were first cleaned by sonication in UP water, acetone, and isopropanol for 10 min each. Then, after drying them with a flow of nitrogen, the substrates were exposed to a plasma discharge at 60 W for 10 min (Harrick Plasma Cleaner, Ithaca, NY, USA). A 50 µL drop of each NP suspension was then placed onto the surface of the substrates and left to dry overnight. Substrates were completely dried under vacuum prior to analysis using a PHI 5600 spectrometer (PerkinElmer) equipped with an Al monochromated 2 mm filament and a built-in charge neutralizer. The X-ray source operated at 350 W, 14.8 V, and 40° take-off angle. The atomic concentrations of sulfur, nitrogen, oxygen, and carbon of drop-casted MMNP and MMNP@PEG samples by performing survey scans between 0 and 1100 eV electron binding energies. Charge correction was performed setting the C 1s peak at 285.0 eV. Data analysis was conducted using MultiPak software version 9.6.015 (Physical Electronics, Chanhassen, MN, USA).
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2

X-ray Photoelectron Spectroscopy of Functionalized Metal Nanoparticles

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Gold-coated silicon substrates were first cleaned by sonication in UP water, acetone, and isopropanol for 10 min each. Then, after drying them with a flow of nitrogen, the substrates were exposed to a plasma discharge at 60 W for 10 min (Harrick Plasma Cleaner, Ithaca, NY, USA). A 50 μL drop of each NP suspension was then placed onto the surface of the substrates and left to dry overnight. Substrates were completely dried under vacuum prior to analysis using a PHI 5600 spectrometer (PerkinElmer) equipped with an Al monochromated 2 mm filament and a built-in charge neutralizer. The X-ray source operated at 350 W, 14.8 V, and 40° take-off angle. The atomic concentrations of sulfur, nitrogen, oxygen, and carbon of drop-casted MMNP and MMNP@PEG samples by performing survey scans between 0 and 1100 eV electron binding energies. Charge correction was performed setting the C 1s peak at 285.0 eV. Data analysis was conducted using MultiPak software version 9.6.015 (Physical Electronics, Chanhassen, MN, USA).
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