ALD and CVD deposition of pure thin gold films from a stable dimethylgold(III) precursor.

The synthesis and thermal properties of a volatile dimethylgold(III) complex MeAuSSP(OPr) are reported. Unlike most other volatile Au(I) and Au(III) compounds, the complex is stable upon storage, does not require any special handling conditions, and exhibits both good volatility and thermal stability. The compound was tested as a CVD and ALD precursor, yielding good quality films in both processes.

Greatly increased electrical conductivity of PBTTT-C14 thin film via controllable single precursor vapor phase infiltration.

Doping is an important strategy for effectively regulating the charge carrier concentration of semiconducting materials. In this study, the electronic properties of organic-inorganic hybrid semiconducting polymers, synthesized viacontrolled vapor phase infiltration (VPI) of poly[2,5-bis(3-tetradecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT-C14) with the metal precursors molybdenum pentachloride (MoCl) and titanium tetrachloride (TiCl), were altered and characterized. The conductivities of the infiltration-doped PBTTT-C14 thin films were enhanced by up to 9 and 4 orders of magnitude, respectively.

Entropy-Driven Self-Healing of Metal Oxides Assisted by Polymer-Inorganic Hybrid Materials.

Enabling self-healing of materials is crucially important for saving resources and energy in numerous emerging applications. While strategies for the self-healing of polymers are advanced, mechanisms for semiconducting inorganic materials are scarce due to the lack of suitable healing agents. Here a concept for the self-healing of metal oxides is developed.

Facile Fabrication of Gold Nanorods@Polystyrenesulfonate Yolk-Shell Nanoparticles for Spaser Applications.

We present a method for producing gold nanorods surrounded by a hollow polymeric shell of polystyrenesulfonate and show that the cavities of such particles can be filled with various organic dyes. The approach consists of covering gold nanorods with silica, followed by its slow hydrolysis in an aqueous medium in the presence of the polymer thin layer permeable for dye molecules. The proposed method enables the yolk-shell nanoparticles to be obtained and loaded with organic dyes without a need to use thermal treatment and/or chemical etching, which makes it suitable for use in the creation of spasers.

Amorphous AlN films grown by ALD from trimethylaluminum and monomethylhydrazine.

The great interest in aluminium nitride thin films has been attributed to their excellent dielectric, thermal and mechanical properties. Here we present the results of amorphous AlN films obtained by atomic layer deposition. We used trimethylaluminum and monomethylhydrazine as the precursors at a deposition temperature of 375-475 °C.

ALD coating of centrifugally spun polymeric fibers and postannealing: case study for nanotubular TiO photocatalyst.

This work describes the synthesis of highly photocatalytically active TiO tubes (TiTBs) by combining centrifugal spinning and atomic layer deposition (ALD). Poly(vinyl pyrrolidone) (PVP) fibers were first produced by centrifugal spinning and subsequently coated with TiO with various film thicknesses in a fluidized bed ALD reactor. After annealing of the TiO ALD coated PVP fibers, TiO tubes (TiTBs) with excellent textural properties and diameters in the range from approx.

Lasing Spaser in Photonic Crystals.

Plasmonic nanolasers (spasers) are of intense interest, attributable to their ability to generate a high-intensity coherent radiation. We infiltrated a three-dimensional silica-based photonic crystal (PhC) film with spasers, composed of spherical gold cores, surrounded by silica shells with dye molecules. In spasers, the gold nanospheres supported the surface plasmons and the dye molecules transferred incoming optical energy to the surface plasmons.

Radical-triggered cross-linking for molecular layer deposition of SiAlCOH hybrid thin films.

Here, we report on a simultaneous growth and radical-initiated cross-linking of a hybrid thin film in a layer-by-layer manner via molecular layer deposition (MLD). The cross-linked film exhibited a self-limiting MLD growth behavior and improved properties like 12% higher film density and enhanced stability compared to the non-cross-linked film.

Omniphobic Etched Aluminum Surfaces with Anti-Icing Ability.

In this work, omniphobic surfaces are developed by combining chemical etching and surface modification of aluminum. In the first step, hierarchical micro/nanostructuring is carried out by chemical etching. Thereafter, a perfluoropolyether is grafted onto the corrugated aluminum substrate, decreasing its surface free energy and turning the system omniphobic.

Molecular layer deposition of hybrid siloxane thin films by ring opening of cyclic trisiloxane (VD) and azasilane.

In this work, we report the first ring opening vapor to solid polymerization of cyclotrisiloxane and N-methyl-aza-2,2,4-trimethylsilacyclopentane by molecular layer deposition (MLD). This process was studied in situ with a quartz crystal microbalance and the thin film was characterized by X-ray photoelectron spectroscopy, ATR-FTIR and high-resolution transmission electron microscopy.

SCIP: a new simultaneous vapor phase coating and infiltration process for tougher and UV-resistant polymer fibers.

The physical properties of polymers can be significantly altered by blending them with inorganic components. This can be done during the polymerization process, but also by post-processing of already shaped materials, for example through coating by atomic layer deposition (ALD) or hybridizing through vapor phase infiltration (VPI), both of which are beneficial in their own way. Here, a new processing strategy is presented, which allows distinct control of the coating and infiltration.

'Sandwich'-like hybrid ZnO thin films produced by a combination of atomic layer deposition and wet-chemistry using a mercapto silane as single organic precursor.

This study describes a straightforward preparation of hybrid organic-inorganic thin films containing a stable 'sandwich'-like structure of two atomic layer deposited (ALD) ZnO layers separated by a thin organosilane phase, which is built from a single organic component (3-mercaptopropyl)trimethoxysilane (MPTMS). Grafting of MPTMS on the first ALD ZnO layer was performed in solution and driven by the strong affinity of the terminal thiol functionality (-SH) towards ZnO. We demonstrate that under different reaction conditions, either MPTMS monolayers are prepared or a 5 nm thick cross-linked polymeric network is formed due to the self-condensation of silane, which covers the ALD ZnO surface.

Building organosilica hybrid nanohemispheres via thiol-ene click reaction on alumina thin films deposited by atomic layer deposition (ALD).

The present work shows a surface-induced preparation of sub-100 nm organosilica nanohemispheres on atomic layer deposited (ALD) AlO thin films, which was achieved by cooperative condensation/hydrolysis and thiol-ene click chemical reactions. The two-step synthetic approach consists of an initial silanization of the AlO film with vinyltrimethoxysilane (VTMS), followed by a photo-promoted growth of surface-bound nanoparticles in the presence of (3-mercaptopropyl)trimethoxysilane (MPTMS). Characterization by means of FE-SEM, XPS and EDS points towards the growth of the nanohemispherical structures being governed by an initial nucleation of thiolated organosilica seeds in solution as a result of self-condensation of MPTMS and oxidation of thiols to disulfides.

Ligand-induced reduction concerted with coating by atomic layer deposition on the example of TiO-coated magnetite nanoparticles.

Atomic layer deposition is a chemical deposition technology that provides ultimate control over the conformality of films and their thickness, even down to Ångström-scale precision. Based on the marked superficial character and gas phase process of the technique, metal sources and their ligands shall ideally be highly volatile. However, in numerous cases those ligands corrode the substrate or compete for adsorption sites, well-known as side reactions of these processes.

Introducing the concept of pulsed vapor phase copper-free surface click-chemistry using the ALD technique.

We report for the first time on a pulsed vapor phase copper-free azide-alkyne click reaction on ZnO by using the atomic layer deposition (ALD) process technology. This reproducible and fast method is based on an in situ two-step reaction consisting of sequential exposures of ZnO to propiolic acid and benzyl azide.

Laponite-Based Surfaces with Holistic Self-Cleaning Functionality by Combining Antistatics and Omniphobicity.

In the present work, perfluoroalkylated laponite nanoparticles with a high degree of functionalization (60 wt %) have been prepared and a methodology to prepare transparent, antistatic, and omniphobic laponite-based films with holistic self-cleaning properties against liquids, solids and liquid-solid mixtures has been developed. The intrinsic electrical and ionic conductivities observed in unmodified laponite coatings are combined with perfluoroalkyl-modified laponite clays. As a result, films with improved self-cleaning functionality based on dust-repellency and omniphobic liquid-repellence (sheet resistance in the range of 10 Ω/□ and contact angles of 106° (HO) and 93° (oil)) were obtained.

Conductive Polymer-Inorganic Hybrid Materials through Synergistic Mutual Doping of the Constituents.

Polymer-matrix-based inorganic-organic hybrid materials are at the cutting edge of current research for their great promise of merging properties of soft and hard solids in one material. Infiltration of polymers with vapors of reactive metal organics is a pathway for postsynthetic blending of the polymer with inorganic materials. Here, we show that this process is also an excellent method for fabricating conductive hybrid materials.

Ferritin-mediated siRNA delivery and gene silencing in human tumor and primary cells.

We demonstrate a straightforward method to encapsulate siRNA into naturally available and unmodified human apoferritin. The encapsulation into apoferritin is independent of the sequence of the siRNA and provides superior protection for those sensitive molecules. High efficiency in transfection can be achieved in human tumorigenic cells, human primary mesenchymal stem cells (hMSC) and peripheral blood mononuclear cells (PBMCs).

Comparison of two endogenous delivery agents in cancer therapy: Exosomes and ferritin.

Exosomes and ferritin: Two biomacromolecules from our human bodies both draw increasing interest for advanced drug delivery due to their endogenous origin and their morphology, the cage-like structures. They possess perfect naturally designed structures for loading and shielding of cargo. Their intrinsic biological functions enable a natural delivery of the load and specific targeting.

Functionalization of Defect Sites in Graphene with RuO2 for High Capacitive Performance.

Graphene is an attractive material for its physicochemical properties, but for many applications only chemically synthesized forms such as graphene oxide (GO) and reduced graphene oxide (rGO) can be produced in sufficient amounts. If considered as electrode material, the intrinsic defects of GO or rGO may have negative influence on the conductivity and electrochemical properties. Such defects are commonly oxidized sites that offer the possibility to be functionalized with other materials in order to improve performance.

Ultrasensitive and label-free molecular-level detection enabled by light phase control in magnetoplasmonic nanoantennas.

Systems allowing label-free molecular detection are expected to have enormous impact on biochemical sciences. Research focuses on materials and technologies based on exploiting localized surface plasmon resonances in metallic nanostructures. The reason for this focused attention is their suitability for single-molecule sensing, arising from intrinsically nanoscopic sensing volume and the high sensitivity to the local environment.

Ferritin light-chain subunits: key elements for the electron transfer across the protein cage.

The first specific functionality of the light-chain (L-chain) subunit of the universal iron storage protein ferritin was identified. The electrons released during iron-oxidation were transported across the ferritin cage specifically through the L-chains and the inverted electron transport through the L-chains also accelerated the demineralization of ferritin.