2022
DOI: 10.3390/catal12020183
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Synthesis and Characterization of Mesoporous Silica Nanoparticles Loaded with Pt Catalysts

Abstract: Coating the catalyst with a nanoporous layer has been demonstrated to be an effective approach to improve catalyst stability. Herein, we systematically investigate two types of core-shell mesoporous silica nanoparticles with a platinum nanocatalyst using a variety of characterization methods. One of the mesoporous particles has a unique amine ring structure in the middle of a shell (Ring-mSiO2/Pt-5.0/SiO2), and the other one has no ring structure (mSiO2/Pt-5.0/SiO2). Brunauer–Emmett–Teller/Barrett–Joyner–Halen… Show more

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Cited by 12 publications
(9 citation statements)
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“…Figure shows representative small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) data for a mesoporous catalytic support with a pore diameter of 2.4 nm. The SAXS profile (Figure a) shows three peaks at positions 1, 3 , and 2 relative to its principal peak ( q *), indicating that the cylindrical pore channels shown in the TEM image (Figure b) are 2D hexagonally ordered. , The second order peak appears as a weak shoulder to the third peak, indicating the presence of a form factor minima …”
Section: Resultsmentioning
confidence: 97%
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“…Figure shows representative small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) data for a mesoporous catalytic support with a pore diameter of 2.4 nm. The SAXS profile (Figure a) shows three peaks at positions 1, 3 , and 2 relative to its principal peak ( q *), indicating that the cylindrical pore channels shown in the TEM image (Figure b) are 2D hexagonally ordered. , The second order peak appears as a weak shoulder to the third peak, indicating the presence of a form factor minima …”
Section: Resultsmentioning
confidence: 97%
“…28,29 The second order peak appears as a weak shoulder to the third peak, indicating the presence of a form factor minima. 29 These strong diffraction peaks from the ordered nanochannels allow monitoring of the infiltration of polymers into the pore in situ, 30 which is demonstrated from simulated SAXS curves (Figure S1) with the analytical scattering formulae of a particle containing ordered pores (see the SI). In principle, the diffraction peak intensity is proportional to the product of the number of particles in the beam N p and the scattering contrast of the porous structure Δρ,…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…For porosity and surface area analysis, the specific surface area of the sample was assessed by BET method and the pore size and pore volume distribution was determined by BJH method using the ASAP 2010 static volumetric absorption analyzer (Micromerities Corp., NY, USA). To remove residual moisture on the particles, samples were degassed by heating at 110 °C for 2 h before nitrogen treatment as the absorbent 37 .…”
Section: Methodsmentioning
confidence: 99%