scholarly journals Electroless deposition of RuO2-based nanoparticles for energy conversion applications

RSC Advances ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 4239-4245 ◽  
Author(s):  
Jing-Mei Li ◽  
Chi-Chang Hu ◽  
Tzu-Ho Wu ◽  
Yung-Jung Hsu

The core/shell VOx·mH2O/RuO2·nH2O, synthesized by simply immersing VOx·mH2O into RuCl3 solution, shows a better catalytic activity of ORR than RuO2·nH2O.

2001 ◽  
Vol 704 ◽  
Author(s):  
M. Toprak ◽  
D. K. Kim ◽  
M. Mikhailova ◽  
Y. Zhang ◽  
Y. K. Jeong ◽  
...  

AbstractNovel metallic capsules containing magnetite with given size in the sub-micron range have been produced. These nanocapsules are prepared in several steps through a colloidal templating approach. The first step is the synthesis of size-selected SiO2 nanospheres. The second step is coating the SiO2nanospheres by electroless deposition with gold, in order to form a porous gold shell around the silica. Electroless deposition is controlled by the concentration of gold in the coating solution. Subsequently, the core (SiO2) was removed to obtain gold capsules. The final step is the inclusion of magnetite nanoparticles inside these nanocapsules and recoating the capsules with gold in order to have continuous encapsulation. The nanocapsule and core-shell structure have been characterized by TEM and DSC


2018 ◽  
Vol 148 (8) ◽  
pp. 2315-2324
Author(s):  
Michelle Lukosi ◽  
Chengcheng Tian ◽  
Xinyi Li ◽  
Shannon M. Mahurin ◽  
Harry M. Meyer ◽  
...  

Soft Matter ◽  
2020 ◽  
Vol 16 (23) ◽  
pp. 5422-5430 ◽  
Author(s):  
Viktor Sabadasch ◽  
Lars Wiehemeier ◽  
Tilman Kottke ◽  
Thomas Hellweg

Responsive non-N-isopropyl acrylamide (non-NIPMA) based core–shell microgels are promising carriers for Pd nanoparticles. The core contains COOH groups to achieve better nanoparticle stabilization. The shell provides control of the catalytic activity.


Nanoscale ◽  
2016 ◽  
Vol 8 (5) ◽  
pp. 2626-2631 ◽  
Author(s):  
Xiaolian Sun ◽  
Dongguo Li ◽  
Shaojun Guo ◽  
Wenlei Zhu ◽  
Shouheng Sun

We optimized the catalytic activity of core/shell Au/FePt nanoparticles (NPs) by finely tuning Au sizes of 4, 7, and 9 nm and FePt shells with similar FePt compositions but 0.5, 1, and 2 nm thickness.


2020 ◽  
Vol 65 (10) ◽  
pp. 904
Author(s):  
V. O. Zamorskyi ◽  
Ya. M. Lytvynenko ◽  
A. M. Pogorily ◽  
A. I. Tovstolytkin ◽  
S. O. Solopan ◽  
...  

Magnetic properties of the sets of Fe3O4(core)/CoFe2O4(shell) composite nanoparticles with a core diameter of about 6.3 nm and various shell thicknesses (0, 1.0, and 2.5 nm), as well as the mixtures of Fe3O4 and CoFe2O4 nanoparticles taken in the ratios corresponding to the core/shell material contents in the former case, have been studied. The results of magnetic research showed that the coating of magnetic nanoparticles with a shell gives rise to the appearance of two simultaneous effects: the modification of the core/shell interface parameters and the parameter change in both the nanoparticle’s core and shell themselves. As a result, the core/shell particles acquire new characteristics that are inherent neither to Fe3O4 nor to CoFe2O4. The obtained results open the way to the optimization and adaptation of the parameters of the core/shell spinel-ferrite-based nanoparticles for their application in various technological and biomedical domains.


Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 72
Author(s):  
Christian Zambrzycki ◽  
Runbang Shao ◽  
Archismita Misra ◽  
Carsten Streb ◽  
Ulrich Herr ◽  
...  

Core-shell materials are promising functional materials for fundamental research and industrial application, as their properties can be adapted for specific applications. In particular, particles featuring iron or iron oxide as core material are relevant since they combine magnetic and catalytic properties. The addition of an SiO2 shell around the core particles introduces additional design aspects, such as a pore structure and surface functionalization. Herein, we describe the synthesis and application of iron-based core-shell nanoparticles for two different fields of research that is heterogeneous catalysis and water purification. The iron-based core shell materials were characterized by transmission electron microscopy, as well as N2-physisorption, X-ray diffraction, and vibrating-sample magnetometer measurements in order to correlate their properties with the performance in the target applications. Investigations of these materials in CO2 hydrogenation and water purification show their versatility and applicability in different fields of research and application, after suitable individual functionalization of the core-shell precursor. For design and application of magnetically separable particles, the SiO2 shell is surface-functionalized with an ionic liquid in order to bind water pollutants selectively. The core requires no functionalization, as it provides suitable magnetic properties in the as-made state. For catalytic application in synthesis gas reactions, the SiO2-stabilized core nanoparticles are reductively functionalized to provide the catalytically active metallic iron sites. Therefore, Fe@SiO2 core-shell nanostructures are shown to provide platform materials for various fields of application, after a specific functionalization.


Micromachines ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 359
Author(s):  
Francesco Ruffino

Bimetallic nanoparticles show novel electronic, optical, catalytic or photocatalytic properties different from those of monometallic nanoparticles and arising from the combination of the properties related to the presence of two individual metals but also from the synergy between the two metals. In this regard, bimetallic nanoparticles find applications in several technological areas ranging from energy production and storage to sensing. Often, these applications are based on optical properties of the bimetallic nanoparticles, for example, in plasmonic solar cells or in surface-enhanced Raman spectroscopy-based sensors. Hence, in these applications, the specific interaction between the bimetallic nanoparticles and the electromagnetic radiation plays the dominant role: properties as localized surface plasmon resonances and light-scattering efficiency are determined by the structure and shape of the bimetallic nanoparticles. In particular, for example, concerning core-shell bimetallic nanoparticles, the optical properties are strongly affected by the core/shell sizes ratio. On the basis of these considerations, in the present work, the Mie theory is used to analyze the light-scattering properties of bimetallic core–shell spherical nanoparticles (Au/Ag, AuPd, AuPt, CuAg, PdPt). By changing the core and shell sizes, calculations of the intensity of scattered light from these nanoparticles are reported in polar diagrams, and a comparison between the resulting scattering efficiencies is carried out so as to set a general framework useful to design light-scattering-based devices for desired applications.


Author(s):  
Yi Guan ◽  
Nan Li ◽  
Jiao He ◽  
Yongliang Li ◽  
Lei Zhang ◽  
...  

Herein, we report a post-assembly strategy by growing the bimetallic Co/Zn zeolitic imidazolate frameworks (BIMZIF) on the surface of the customized Mo metal-organic frameworks (MOFs) (Mo-MOF) to prepare the core-shell...


Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 502
Author(s):  
Karel Šindelka ◽  
Zuzana Limpouchová ◽  
Karel Procházka

Using coarse-grained dissipative particle dynamics (DPD) with explicit electrostatics, we performed (i) an extensive series of simulations of the electrostatic co-assembly of asymmetric oppositely charged copolymers composed of one (either positively or negatively charged) polyelectrolyte (PE) block A and one water-soluble block B and (ii) studied the solubilization of positively charged porphyrin derivatives (P+) in the interpolyelectrolyte complex (IPEC) cores of co-assembled nanoparticles. We studied the stoichiometric mixtures of 137 A10+B25 and 137 A10−B25 chains with moderately hydrophobic A blocks (DPD interaction parameter aAS=35) and hydrophilic B blocks (aBS=25) with 10 to 120 P+ added (aPS=39). The P+ interactions with other components were set to match literature information on their limited solubility and aggregation behavior. The study shows that the moderately soluble P+ molecules easily solubilize in IPEC cores, where they partly replace PE+ and electrostatically crosslink PE− blocks. As the large P+ rings are apt to aggregate, P+ molecules aggregate in IPEC cores. The aggregation, which starts at very low loadings, is promoted by increasing the number of P+ in the mixture. The positively charged copolymers repelled from the central part of IPEC core partially concentrate at the core-shell interface and partially escape into bulk solvent depending on the amount of P+ in the mixture and on their association number, AS. If AS is lower than the ensemble average ⟨AS⟩n, the copolymer chains released from IPEC preferentially concentrate at the core-shell interface, thus increasing AS, which approaches ⟨AS⟩n. If AS>⟨AS⟩n, they escape into the bulk solvent.


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