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Dielectric materials are of great interest in a vast amount of applications ranging from cable insulation to advanced electronic devices. The emerging trend of device miniaturization is creating an increased demand for dielectric thin films that can be produced precisely on the nanometer scale. In addition, special mechanical properties are often required, for example in the field of flexible organic electronics. Polymers are first-choice materials for this purpose. However, it is extremely difficult to produce precise nanoscale thin films, which have a low defect density and are free of e.g. residual solvent, by wet chemistry approaches. Initiated chemical vapor deposition (iCVD) is a solvent-free polymer thin film deposition process which can be used to produce high quality dielectric thin films with nanoscale control and circumvents thus these problems. This work demonstrates the versatility of the iCVD process in the field of electrical applications by some new application examples of iCVD. By adding e.g. a hydrophobic organosiloxane thin film on columnar zinc oxide (ZnO:Fe) gas sensing structures there was a change in the selectivity from ethanol to hydrogen, as well as improved performance at high humidity level. The modified sensors can thus be used in humid ambient, especially for breathing tests, which can lead to the diagnosis of some diseases by cutting edge non-invasive approaches.

Mixed metal oxide (MMO) nanoparticles (NPs) are hybrids consisting of two or more nanoscale metal oxides. Advantages of MMO NPs over single metal oxides include improved catalytic activity, enhanced electrical and magnetic properties, and increased thermal stability due to the synergy of the different oxide components. This study presents a novel fabrication route for TiO2‐CeO2 NPs enriched with oxygen vacancies using a Haberland‐type gas aggregation cluster source. The NPs, deposited from different segmented Ti/Ce targets under varying O2 addition, were examined with respect to final composition, morphology, and Ti, Ce surface oxidation states. Particle formation mechanisms are proposed for the observed morphologies. Additionally, available O2 during deposition and its impact on the formation of defective sites were investigated. Defective sites in TiO2‐CeO2 NPs were analyzed using transfer to X‐ray photoelectron spectroscopy and transmission electron microscopy without contact to ambient oxygen. The incorporation of Ce to the target exhibits synergistic effects on the synthesis process. Segmented Ti/Ce targets enable the deposition of a broad range of mixed oxide NPs with diverse compositions and morphologies at considerably enhanced deposition rates, which is vital for practical applications. The presented fabrication approach is expected to be applicable for a broad variety of MMO NPs. [ABSTRACT FROM AUTHOR]

The new generation of laser-based solid-state lighting (SSL) white light sources requires new material systems capable of withstanding, diffusing, and converting high intensity laser light. State-of-the-art systems use a blue light emitting diode or laser diode in combination with color conversion materials, such as yellow emitting Ce-doped phosphors or red and green emitting quantum dots (QD), to produce white light. However, for laser-based high-brightness illumination thermal management and uniform light diffusion are still major challenges in the quest to convert a highly focused laser beam into an efficient lighting solution. Here, we present a material system consisting of a highly open porous (> 99%) framework structure of hollow SiO2 microtubes. This framework structure enables efficient and uniform light distribution as well as ensuring good thermal management even at high laser powers of up to 5 W, while drastically reducing the speckle contrast. By further functionalizing the microtubes with halide perovskite QDs (SiO2@CsPbBr3 as model system) color conversion from UV to visible light is achieved. By depositing an ultrathin (~ 5.5 nm) film of poly(ethylene glycol dimethyl acrylate) (pEGDMA) via initiated chemical vapor deposition (iCVD), the luminescent stability of the QDs against moisture is enhanced. The demonstrated hybrid material system paves the way for the design of advanced and functional laser light diffusers and converters that can meet the challenges associated with laser-based SSL applications. [ABSTRACT FROM AUTHOR]

In recent years, defective TiO2 has caught considerable research attention because of its potential to overcome the limits of low visible light absorption and fast charge recombination present in pristine TiO2 photocatalysts. Among the different synthesis conditions for defective TiO2, ambient pressure hydrogenation with the addition of Ar as inert gas for safety purposes has been established as an easy method to realize the process. Whether the Ar gas might still influence the resulting photocatalytic properties and defective surface layer remains an open question. Here, we reveal that the gas flow ratio between H2 and Ar has a crucial impact on the defective structure as well as the photocatalyic activity of TiO2. In particular, transmission electron microscopy (TEM) in combination with electron energy loss spectroscopy (EELS) revealed a larger width of the defective surface layer when using a H2/Ar (50 %–50 %) gas mixture over pure H2. A possible reason could be the increase in dynamic viscosity of the gas mixture when Ar is added. Additionally, photoinduced enhanced Raman spectroscopy (PIERS) is implemented as a complementary approach to investigate the dynamics of the defective structures under ambient conditions which cannot be effortlessly realized by vacuum techniques like TEM. [ABSTRACT FROM AUTHOR]

In the strive for energy efficient computing, many different neuromorphic computing and engineering schemes have been introduced. Nanoparticle networks (NPNs) at the percolation threshold have been established as one of the promising candidates, e.g., for reservoir computing because among other useful properties they show self‐organization and brain‐like avalanche dynamics. The dynamic resistance changes trace back to spatio‐temporal reconfigurations in the connectivity upon resistive switching in distributed memristive nano‐junctions and nano‐gaps between neighboring nanoparticles. Until now, however, there has not yet been any direct imaging or monitoring of current paths in NPN. In this study, an NPN comprising of Ag/CxOyHz core/shell and Ag nanoparticles at the percolation threshold is reported. It is shown that this NPN is within a critical regime, exhibiting avalanche dynamics. To monitor in situ the evolving current paths in this NPN, active voltage contrast and resistive contrast imaging are used complementarily. Including simulations, the results provide experimental insight toward understanding the complex current response of the memristive NPN. As such, this study paves the way toward an experimental characterization of dynamic reorganizations in current paths inside NPN, which is highly relevant for validating and improving simulations and finally establishing a deeper understanding of switching dynamics in NPNs. [ABSTRACT FROM AUTHOR]

Certain biomarkers in exhaled breath are indicators of diseases in the human body. The non-invasive detection of such biomarkers in human breath increases the demand for simple and cost-effective gas sensors to replace state-of-the-art gas chromatography (GC) machines. The use of metal oxide (MOX) gas sensors based on thin-film structures solves the current limitations of breath detectors. However, the response at high humidity levels, i.e., in the case of exhaled human breath, significantly decreases the sensitivity of MOX sensors, making it difficult to detect small traces of biomarkers. We have introduced, in previous work, the concept of a hybrid gas sensor, in which thin-film-based MOX gas sensors are combined with an ultra-thin (20–30 nm) polymer top layer deposited by solvent-free initiated chemical vapor deposition (iCVD). The hydrophobic top layer enables sensor measurement in high-humidity conditions as well as the precise tuning of selectivity and sensitivity. In this paper, we present a way to increase the hydrogen (H2) sensitivity of hybrid sensors through chemical modification of the polymer top layer. A poly(1,3,5,7-tetramethyl-tetravinylcyclotetrasiloxane) (PV4D4) thin film, already applied in one of our previous studies, is transformed into a silsesquioxane-containing top layer by a simple heating step. The transformation results in a significant increase in the gas response for H2 ~709% at an operating temperature of 350 °C, which we investigate based on the underlying sensing mechanism. These results reveal new pathways in the biomedical application field for the analysis of exhaled breath, where H2 indicates gastrointestinal diseases. [ABSTRACT FROM AUTHOR]