Evolved stars are a foundry of chemical complexity, gas and dust that provides the building blocks of planets and life, and dust nucleation first occurs in their photosphere. Despite their importance, the circumstellar regions enveloping these stars remain hidden to many observations, thus dust formation processes are still poorly understood. Laboratory astrophysics provides complementary routes to unveil these chemical processes, but most experiments rely on combustion or plasma Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:

The ionic polymerization of acetylene in cold plasmas of C 2 H 2 /He and C 2 H 2 /Ar has been experimentally studied and modeled in radio frequency (rf) discharges with conditions selected to avoid particle formation. Steady-state distributions of positive and negative ions were measured with mass spectrometry. All the measured distributions are dominated by ions with an even number of carbon atoms, reflecting the characteristic polyyne structures typical for the polymerization of acetylene. The distributions show a monotonic decrease in intensity from ions with two carbon atoms until the highest number of atoms detected. For cations, the distributions extend until 12 carbon atoms. The anion distributions extend further, and negative ions with 20 C atoms are observed in the C 2 H 2 /Ar plasma. From the measured mass spectra it is not possible to decide on the possible presence of aromatic species in ions with more than six carbon atoms. A simple model assuming a homogeneous discharge was used to describe the plasma kinetics and could account for the measured ion distributions with reasonable values of charge density and electron temperature. The results of this work stress the important role of the vinylidene anion and indicate that Ar and He do not have much influence on the carbon chemistry.

The increasing demand for nanostructured materials is mainly motivated by their key role in a wide variety of technologically relevant fields such as biomedicine, green sustainable energy or catalysis. We have succeeded to scale-up a type of gas aggregation source, called a multiple ion cluster source, for the generation of complex, ultra-pure nanoparticles made of different materials. The high production rates achieved (tens of g/day) for this kind of gas aggregation sources, and the inherent ability to control the structure of the nanoparticles in a controlled environment, make this equipment appealing for industrial purposes, a highly coveted aspect since the introduction of this type of sources. Furthermore, our innovative UHV experimental station also includes in-flight manipulation and processing capabilities by annealing, acceleration, or interaction with background gases along with in-situ characterization of the clusters and nanoparticles fabricated. As an example to demonstrate some of the capabilities of this new equipment, herein we present the fabrication of copper nanoparticles and their processing, including the controlled oxidation (from Cu0 to CuO through Cu2O, and their mixtures) at different stages in the machine.

Interstellar carbonaceous dust is mainly formed in the innermost regions of circumstellar envelopes around carbonrich asymptotic giant branch stars (AGBs). In these highly chemically stratified regions, atomic and diatomic carbon, along with acetylene, are the most abundant species after H 2 and CO. In a previous study, we addressed the chemistry of carbon (C and C 2 ) with H 2 showing that acetylene and aliphatic species form efficiently in the dust formation region of carbon-rich AGBs whereas aromatics do not. Still, acetylene is known to be a key ingredient in the formation of linear polyacetylenic chains, benzene, and polycyclic aromatic hydrocarbons (PAHs), as shown by previous experiments. However, these experiments have not considered the chemistry of carbon (C and C 2 ) with C 2 H 2 . In this work, by employing a sufficient amount of acetylene, we investigate its gas-phase interaction with atomic and diatomic carbon. We show that the chemistry involved produces linear polyacetylenic chains, benzene, and other PAHs, which are observed with high abundances in the early evolutionary phase of planetary nebulae. More importantly, we have found a nonnegligible amount of pure and hydrogenated carbon clusters as well as aromatics with aliphatic substitutions, both being a direct consequence of the addition of atomic carbon. The incorporation of alkyl substituents into aromatics can be rationalized by a mechanism involving hydrogen abstraction followed by methyl addition. All the species detected in the gas phase are incorporated into nanometricsized dust analogs, which consist of a complex mixture of sp, sp 2 , and sp 3 hydrocarbons with amorphous morphology.

Integrating an absorbing thin film into a resonant cavity is the most practical way to achieve perfect absorption of light at a selected wavelength in the mid-to-far infrared, as required to target blackbody radiation or molecular fingerprints. The cavity is designed to resonate and enable perfect absorption in the film at the chosen wavelength . However, in current state-ofthe-art designs, a still large absorbing film thickness ( /50) is needed and tuning the perfect absorption wavelength over a broad range requires changing the cavity materials. Here, we introduce a new resonant cavity concept to achieve perfect absorption of infrared light in much thinner and thus really nanoscale films, with a broad wavelength tunability using a single set of cavity materials. It requires a nanofilm with giant refractive index and small extinction coefficient (found in emerging semi-metals, semi-conductors and topological insulators) backed by a transparent spacer and a metal mirror. The nanofilm acts both as absorber and multiple reflector for the internal cavity waves, which after escaping follow a fractal phasor trajectory. This enables a totally destructive optical interference for a nanofilm thickness more than 2 orders of magnitude smaller than . With this remarkable effect, we demonstrate angle-insensitive perfect absorption in sub -/100 bismuth nanofilms, at a wavelength tunable from 3 to 20 m.