scholarly journals Mesocrystals from Platinum Nanocubes

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2122
Author(s):  
Christian Jenewein ◽  
Helmut Cölfen
Keyword(s):  
Particle Size ◽  
Atomic Scale ◽  
Crystal Habit ◽  
Ongoing Research ◽  
X Ray ◽  
X Ray Scattering ◽  
Nanoparticle Dispersions ◽  
Reproducible Method ◽  
Catalytic Applications ◽  
High Degree

Platinum nanoparticles are widely known for their numerous electrochemical and catalytic applications. Enhanced or novel properties that may arise when ordering such particles in a highly defined manner, however, are still subject to ongoing research, as superstructure formation on the mesoscale is still a major challenge to be overcome. In this work, we therefore established a reproducible method to fabricate micrometer-sized superstructures from platinum nanocubes. Through small-angle X-ray scattering and electron diffraction methods we demonstrate that the obtained superstructures have a high degree of ordering up to the atomic scale and, therefore, fulfill all criteria of a mesocrystal. By changing the solvent and stabilizer in which the platinum nanocubes were dispersed, we were able to control the resulting crystal habit of the mesocrystals. Aside from mesocrystal fabrication, this method can be further utilized to purify nanoparticle dispersions by recrystallization with respect to narrowing down the particle size distribution and removing contaminations.

scholarly journals Reversible magnetism switching of iron oxide nanoparticle dispersions by controlled agglomeration

2021 ◽  
Author(s):  
Stephan Müssig ◽  
Björn Kuttich ◽  
Florian Fidler ◽  
Daniel Haddad ◽  
Susanne Wintzheimer ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Iron Oxide ◽  
Light Scattering ◽  
Superparamagnetic Iron Oxide ◽  
Iron Oxide Nanoparticle ◽  
Oxide Nanoparticles ◽  
X Ray ◽  
X Ray Scattering ◽  
Nanoparticle Dispersions ◽  
Oxide Nanoparticle

The controlled agglomeration of superparamagnetic iron oxide nanoparticles (SPIONs) was used to rapidly switch their magnetic properties. Small-angle X-ray scattering (SAXS) and dynamic light scattering showed that tailored iron oxide...

scholarly journals Synthesis and Advanced Characterization of Polymer-Protein Core-Shell Nanoparticles

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 730
Author(s):  
Erik Sarnello ◽  
Tao Li
Keyword(s):  
Particle Size ◽  
Small Angle ◽  
Core Shell ◽  
Assembly Process ◽  
Shell Nanoparticles ◽  
X Ray ◽  
X Ray Scattering ◽  
Wide Range ◽  
Core Shell Nanoparticles ◽  
Ray Scattering

Enzyme immobilization techniques are widely researched due to their wide range of applications. Polymer–protein core–shell nanoparticles (CSNPs) have emerged as a promising technique for enzyme/protein immobilization via a self-assembly process. Based on the desired application, different sizes and distribution of the polymer–protein CSNPs may be required. This work systematically studies the assembly process of poly(4-vinyl pyridine) and bovine serum albumin CSNPs. Average particle size was controlled by varying the concentrations of each reagent. Particle size and size distributions were monitored by dynamic light scattering, ultra-small-angle X-ray scattering, small-angle X-ray scattering and transmission electron microscopy. Results showed a wide range of CSNPs could be assembled ranging from an average radius as small as 52.3 nm, to particles above 1 µm by adjusting reagent concentrations. In situ X-ray scattering techniques monitored particle assembly as a function of time showing the initial particle growth followed by a decrease in particle size as they reach equilibrium. The results outline a general strategy that can be applied to other CSNP systems to better control particle size and distribution for various applications.

Tracking the Catalyst Layer Depth-Dependent Electrochemical Degradation of a Bimodal Pt/C Fuel Cell Catalyst: A Combined Operando Small- and Wide-Angle X-Ray Scattering Study

2021 ◽  
Author(s):  
Johanna Schröder ◽  
Rebecca K. Pittkowski ◽  
Isaac Martens ◽  
Raphaël Chattot ◽  
Jakub Drnec ◽  
...  
Keyword(s):  
Particle Size ◽  
Fuel Cell ◽  
Ostwald Ripening ◽  
Catalyst Layer ◽  
Wide Angle ◽  
Layer Depth ◽  
X Ray ◽  
Fuel Cell Catalyst ◽  
X Ray Scattering ◽  
Size Population

The combination of operando small- and wide-angle X-ray scattering (SAXS, WAXS) is here presented to provide insights into the changes in mean particle sizes and phase fractions in fuel cell catalyst layers during accelerated stress tests (ASTs). As fuel cell catalyst, a bimodal Pt/C catalyst was chosen that consists of two distinguishable particle size populations. The presence of the two different sizes should favor and uncover electrochemical Ostwald ripening as degradation mechanism, i.e., the growth of larger particles in the Pt/C catalyst at the expense of the smaller particles via the formation of ionic metal species. However, instead of electrochemical Ostwald ripening, the results point toward classical Ostwald ripening via the local diffusion of metal atoms on the support. Furthermore, the grazing incidence mode provides insights into the catalyst layer depth-dependent degradation. While the larger particles show the same particle size changes close to the electrolyte-catalyst interface and within the catalyst layer, the smaller Pt nanoparticles exhibit a slightly decreased size at the electrolyte-catalyst interface. During the AST, both size populations increase in size, independent of the depth. Their phase fraction, i.e., the ratio of smaller to larger size population, however, exhibits a depth-dependent behavior. While at the electrolyte-catalyst interface the phase fraction of the smaller size population decreases, it increases in the inner catalyst layer. The results of a depth-dependent degradation suggest that employing a depth-dependent catalyst design can be used for future improvement of catalyst stability.

scholarly journals Nitrosative stress sensing inPorphyromonas gingivalis: structure of and heme binding by the transcriptional regulator HcpR

2019 ◽  
Vol 75 (4) ◽  
pp. 437-450 ◽  
Author(s):  
B. Ross Belvin ◽  
Faik N. Musayev ◽  
John Burgner ◽  
J. Neel Scarsdale ◽  
Carlos R. Escalante ◽  
...  
Keyword(s):  
Molecular Mechanisms ◽  
Nitrosative Stress ◽  
Gas Sensing ◽  
Anaerobic Bacteria ◽  
Heme Iron ◽  
Heme Binding ◽  
X Ray ◽  
X Ray Scattering ◽  
Stress Sensing ◽  
High Degree

Although the HcpR regulator plays a vital step in initiation of the nitrosative stress response in many Gram-negative anaerobic bacteria, the molecular mechanisms that it uses to mediate gas sensing are not well understood. Here, a 2.6 Å resolution crystal structure of the N-terminal sensing domain of the anaerobic periodontopathogenPorphyromonas gingivalisHcpR is presented. The protein has classical features of the regulators belonging to the FNR-CRP family and contains a hydrophobic pocket in its N-terminal sensing domain. It is shown that heme bound to HcpR exhibits heme iron as a hexacoordinate system in the absence of nitric oxide (NO) and that upon nitrosylation it transitions to a pentacoordinate system. Finally, small-angle X-ray scattering experiments on full-length HcpR reveal that the C-terminal DNA-binding domain of HcpR has a high degree of interdomain flexibility.

Atomic scale characterization of organometallic vapor phase epitaxial growth using in-situ grazing incidence X-ray scattering

1992 ◽  
Vol 124 (1-4) ◽  
pp. 1-9 ◽  
Author(s):  
D.W. Kisker ◽  
G.B. Stephenson ◽  
P.H. Fuoss ◽  
F.J. Lamelas ◽  
S. Brennan ◽  
...  
Keyword(s):  
Epitaxial Growth ◽  
Vapor Phase ◽  
Grazing Incidence ◽  
Atomic Scale ◽  
X Ray ◽  
X Ray Scattering ◽  
Scale Characterization ◽  
Ray Scattering

scholarly journals Structural Study of the Photo-Mediated Growth of Silver Nanoprisms

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5413
Author(s):  
Matti Knaapila ◽  
Ulla Vainio ◽  
Sophie E. Canton ◽  
Gunnel Karlsson
Keyword(s):  
Particle Size ◽  
Small Angle ◽  
Volume Ratio ◽  
Direct Methods ◽  
Saxs Data ◽  
Aqueous Dispersions ◽  
X Ray ◽  
Silver Nanoprisms ◽  
X Ray Scattering ◽  
Ag Particles

We present a small-angle X-ray scattering (SAXS) study of the anisotropic photoinduced growth of silver (Ag) nanoprisms in aqueous dispersions. The growth of nearly spherical (<10 nm) Ag particles into large (>40 nm) and thin (<10 nm) triangular nanoprisms induced by 550 nm laser is followed in terms of particle size using indirect and direct methods for irradiation times up to 150 min. During the process, the surface-to-volume ratio of the particles decreased. The SAXS data of the initial solution fit well to the model of polydisperse spheres with pronounced average diameters around 7.4 nm and 10 nm. The data after 45 min irradiation fit well to the model containing approximately the same amount of the initial particles and the end product, the nanoprisms.

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