In alloyed nanoparticles, synergistic electronic and/or geometric effects may enhance the catalytic properties compared to their monometallic counterparts. Herein, we address synthesis of bimetallic Au/Cu nanoparticles with different compositions by wet chemical reduction in ionic liquids. The were successively supported on carbon. liquid could be recycled after synthesis. Annealing carbon-supp...

An embedded-domain phase-field formalism is used for studying phase transformation pathways in bimetallic nanoparticles (BNPs). Competition of bulk and surface-directed spinodal decomposition processes their interplay with capillarity are identified as the main determinants BNP morphology. The former characterized by an effective driving force $\Delta\tilde{f}$ which increases decreasing temper...

Colloidal or heterogeneous nanocatalysts can improve the range and diversity of Cu(I)-catalysed click reactions and facilitate catalyst separation and reuse. Catalysis by metal nanoparticles raises the question as to whether heterogeneous catalysts may cause homogeneous catalysis through metal ion leaching, since the catalytic process could be mediated by the particle, or by metal ions released...

The composite framework of graphitic carbon nitride (gCN) supported copper nanoparticle can act as a high-performance photoreactor for the synthesis of 1,2,3-triazole derivatives under light irradiation in the absence of alkaline condition. The photoactivity of gCN originates from an electron transition from the valence band to the conduction band, in the presence of photon energy, and the hot ...

A peptide sequence N(3)-GVGV-OMe (G: glycine; V: valine) was attached to a benzene 1,3,5-tricarboxamide (BTA) derivative via"click chemistry" to afford a C(3)-symmetric artificial oligopeptide. The key feature of this oligopeptide is that the binding sites (triazole groups formed by click reaction) are located at the center, while the three oligopeptide arms with a strong tendency to assemble a...

We report for the first time the synthesis of unimolecular polystyrene-based nanoparticles (PS-NPs) under normal air atmosphere by direct carbon-carbon “click” chemistry (i.e., “self-click” chemistry). First, statistical poly(styrene-co-4-vinylbenzyl chloride) copolymers synthesized by RAFT polymerization were decorated in a facile manner with alkyne groups by reaction with potassium propiolate...

The boundary layer flow of Cu-water based nanofluid with heat transfer over a stretching sheet is numerically studied. Second order velocity slip flow model is considered instead of no-slip at the boundary. The governing partial differential equations are transformed into ordinary one using similarity transformation, before being solved numerically. Numerical solutions of these equations are ob...

Due to their excess surface free energy and structural instabilities, nanoparticles exhibit interesting physical and chemical properties. There has been an ever-growing interest in investigating these properties, driven by the desire to further miniaturize electronic devices, develop new functional materials and catalysts. Here, the intriguing question of how diffusion evolves in a single nanop...

We demonstrate the use of "click" chemistry to form electrochemically and photoelectrochemically active molecular interfaces to SnO(2) nanoparticle thin films. By using photochemical grafting to link a short-chain alcohol to the surface followed by conversion to a surface azide group, we enable use of the Cu(I)-catalyzed azide-alkyne [3 + 2] cycloaddition (CuAAC) reaction, a form of "click" che...

We report that a histidine based cationic lipid forms multi-bilayer nanotubes and the addition of metal ions such as Cu(2+) and Au(3+) induces transformation into single-bilayer nanotubes owing to coordination of the metal ions on the nanotube surface. The morphological transition was detected with X-ray scattering and electron microscopy. IR showed that the metal coordination is presumably the...