Synthesis and studying properties of the GNPs@FexOy structure

An article presents a study of the regularities of the formation of gold up to 8 nm thick, deposited by vacuum thermal deposition on silicon wafers with a natural oxide, its annealing and subsequent deposition of iron oxide by chemical vapor deposition. The stages were accompanied by SEM analysis of the sample surface, as well as fixation of the optical and FTIR spectra, I–V characteristics of the obtained structures.

Reverse Engineering of Thin Films to Nanoparticles by Thermal Deposition for Large-Scale Production of Nanometals

A simple method to synthesize metal nanoparticles (Nps) has been proposed using high vacuum thermal deposition (HVTD) by reverse engineering of thin films to Nps. Metal Nps synthesized by this technique corresponds to the top-down approach of nanomaterial synthesis from bulk metals of silver and copper wires to metal Nps. A high-vacuum thermal deposition is a commonly used technique for thin-film deposition in many applications. Synthesis of metal Nps by HVTD is simple, efficient, and can provide particle of about few tens of nanometers is effortless. A precoated thin layer of polyethylene glycol (PEG) on a glass substrate (Petri dish), is allowed deposit with a metallic thin film by thermionically evaporating bulk metal wires in high vacuum. The deposited metal thin film is removed along with the PEG coating into a liquid medium and subjected to sonication, stirring, and deoxidation. Obtaining the particle size in tens of nanometer range in one step is one projecting factor by HVTD technique. Also, providing the feasibility of reusing large particles as precursors after synthesis is a unique vantage point. The Nps were analyzed by various characterizations tools to evaluate the underlying properties.

Bilayer Thin Films That Combine Luminescent and Spin Crossover Properties for an Efficient and Reversible Fluorescence Switching

We report on the vacuum thermal deposition of bilayer thin films of the luminescent complex Ir(ppy)3, tris[2-phenylpyridinato-C2,N]iridium(III), and the spin crossover complex [Fe(HB(tz)3)2], bis[hydrotris(1,2,4-triazol-1-yl)borate]iron(II). Switching the spin state of iron ions from the low spin to the high spin state around 337 K leads to a reversible jump of the luminescence intensity, while the spectrum shape and the luminescence lifetime remain unchanged. The luminescence modulation occurs due to the different UV light absorption properties of the iron complex in the two spin states and its magnitude can therefore be precisely adjusted by varying the film thickness. These multilayer luminescence switches hold potential for micro- and nanoscale thermal sensing and imaging applications.