arXiv subjects

G. Mulas

Publications and source records attributed to G. Mulas.

At least 19 recordsLinked to original sources

arXiv2026

Nano-particle Transition Matrix code implementation

Electromagnetic scattering and absorption by material particles is a fundamental physical problem with a broad range of applications, going from laboratory experiments, biology and material sciences, all the way up to environmental studies and astrophysical investigations. In spite of its primary importance, an exact theoretical treatment is only possible for a limited range of ideal cases, while realistic situations require the development of numerical solutions. In the course of the years, several techniques were developed to model the effects of scattering and absorption in more general cases, using approaches such as the Discrete Dipole Approximation (DDA), the Finite Difference Time Domain (FDTD) method, the Transition Matrix formalism (T-matrix) or the Mean Field Theory (MFT). Among these possibilities, the T-matrix approach grants the highest degree of flexibility in modeling aggregates of spherically symmetric particles with arbitrary overall morphology and composition, but its application has been limited by the challenging computational requirements of the method in realistic cases. This paper describes the Nano-Particle Transition Matrix Code project (NP_TMcode), a new implementation of the T-matrix formalism that, taking advantage of high performance parallel hardware architectures, allows the solution of increasingly complex models, while substantially reducing the computing time. The paper describes the code structure, with a particular focus on the algorithm optimization, and it presents the results of the performance analysis for a set of development applications.

astro-ph.IM↗

arXiv2025

Interstellar dust as a dynamic environment

In spite of accounting for only a small fraction of the mass of the Interstellar Medium (ISM), dust plays a primary role in many physical and chemical processes in the Universe. It is the main driver of extinction of radiation in the UV/optical wavelength range and a primary source of thermal IR emission. Dust grains contain most of the refractory elements of the ISM and they host chemical processes that involve complex molecular compounds. However, observational evidence suggests that grain structure is highly non-trivial and that dust particles are characterized by granularity, asymmetry and stratification, which significantly affect their interaction with radiation fields. Accurate modeling of such interaction is fundamental to properly explain observational results, but it is a computationally demanding task. Here we present the possibility to investigate the effects of radiation/particle interactions in non-spherically symmetric conditions using a novel implementation of the Transition Matrix formalism, designed to run on scalable parallel hardware facilities.

astro-ph.GA↗

arXiv2017

Detection of Buckminsterfullerene emission in the diffuse interstellar medium

Emission of fullerenes in their infrared vibrational bands has been detected in space near hot stars. The proposed attribution of the diffuse interstellar bands at 9577 and 9632 \AA\ to electronic transitions of the buckminsterfullerene cation (i.e. C$_{60}^+$ ) was recently supported by new laboratory data, confirming the presence of this species in the diffuse interstellar medium (ISM). In this letter, we present the detection, also in the diffuse ISM, of the 17.4 and 18.9 $\mu$m emission bands commonly attributed to vibrational bands of neutral C$_{60}$. According to classical models that compute the charge state of large molecules in space, C$_{60}$ is expected to be mostly neutral in the diffuse ISM. This is in agreement with the abundances of diffuse C$_{60}$ we derive here from observations.

astro-ph.GA↗

arXiv2015

30 years of cosmic fullerenes

In 1985, "During experiments aimed at understanding the mechanisms by which long-chain carbon molecules are formed in interstellar space and circumstellar shells", Harry Kroto and his collaborators serendipitously discovered a new form of carbon: fullerenes. The most emblematic fullerene (i.e. C$_{60}$ "buckminsterfullerene"), contains exactly 60 carbon atoms organized in a cage-like structure similar to a soccer ball. Since their discovery impacted the field of nanotechnologies, Kroto and colleagues received the Nobel prize in 1996. The cage-like structure, common to all fullerene molecules, gives them unique properties, in particular an extraordinary stability. For this reason and since they were discovered in experiments aimed to reproduce conditions in space, fullerenes were sought after by astronomers for over two decades, and it is only recently that they have been firmly identified by spectroscopy, in evolved stars and in the interstellar medium. This identification offers the opportunity to study the molecular physics of fullerenes in the unique physical conditions provided by space, and to make the link with other large carbonaceous molecules thought to be present in space : polycyclic aromatic hydrocarbons.

astro-ph.GA↗

arXiv2015

Redshifted Diffuse Interstellar Bands in Orion OB1 association

The wavelength displacement of the Diffuse Interstellar Bands at 4502, 5705, 5780, 6284, and 7224 \AA\ with respect to the well known, narrow atomic/molecular interstellar lines (of Ca{\sc ii} and Na{\sc i}) have been measured in the spectra of the 2 Orion Trapezium stars HD 37022 and HD 37020, using the HARPS\textendash N spectrograph, fed with the 3.5 m Telescopio Nazionale Galileo, and the BOES spectrograph, fed with the 1.8m Korean telescope. The red shift is $\sim$25 km/s for all these DIBs. We discuss the various possible origins of this very peculiar wavelength shift in the light of the particular physical conditions in the Orion Trapezium. The above mentioned shift is seemingly absent in the DIBs at 6196 and 6993 \AA.

astro-ph.GA↗

arXiv2011

Electronic and optical properties of families of polycyclic aromatic hydrocarbons: a systematic (time-dependent) density functional theory study

Homologous classes of Polycyclic Aromatic Hydrocarbons (PAHs) in their crystalline state are among the most promising materials for organic opto-electronics. Following previous works on oligoacenes we present a systematic comparative study of the electronic, optical, and transport properties of oligoacenes, phenacenes, circumacenes, and oligorylenes. Using density functional theory (DFT) and time-dependent DFT we computed: (i) electron affinities and first ionization energies; (ii) quasiparticle correction to the highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) gap; (iii) molecular reorganization energies; (iv) electronic absorption spectra of neutral and $\pm1$ charged systems. The excitonic effects are estimated by comparing the optical gap and the quasiparticle corrected HOMO-LUMO energy gap. For each molecular property computed, general trends as a function of molecular size and charge state are discussed. Overall, we find that circumacenes have the best transport properties, displaying a steeper decrease of the molecular reorganization energy at increasing sizes, while oligorylenes are much more efficient in absorbing low-energy photons in comparison to the other classes.

cond-mat.mtrl-sci↗

arXiv2010

Visible photodissociation spectroscopy of PAH cations and derivatives in the PIRENEA experiment

The electronic spectra of gas-phase cationic polycyclic aromatic hydrocarbons (PAHs), trapped in the Fourier Transform Ion Cyclotron Resonance cell of the PIRENEA experiment, have been measured by multiphoton dissociation spectroscopy in the 430-480 nm spectral range using the radiation of a mid-band optical parametric oscillator laser. We present here the spectra recorded for different species of increasing size, namely the pyrene cation (C16H10+), the 1-methylpyrene cation (CH3-C16H9+), the coronene cation (C24H12+), and its dehydrogenated derivative C24H10+. The experimental results are interpreted with the help of time-dependent density functional theory calculations and analysed using spectral information on the same species obtained from matrix isolation spectroscopy data. A kinetic Monte Carlo code has also been used, in the case of pyrene and coronene cations, to estimate the absorption cross-sections of the measured electronic transitions. Gas-phase spectra of highly reactive species such as dehydrogenated PAH cations are reported for the first time.

physics.chem-ph↗

arXiv2009

Polycyclic aromatic hydrocarbons with SPICA

Thanks to high sensitivity and angular resolution and broad spectral coverage, SPICA will offer a unique opportunity to better characterize the nature of polycyclic aromatic hydrocarbons (PAHs) and very small grains (VSGs), to better use them as probes of astrophysical environments. The angular resolution will enable to probe the chemical frontiers in the evolution process from VSGs to neutral PAHs, to ionized PAHs and to "Grand-PAHs" in photodissotiation regions and HII regions, as a function of G$_0$/n (UV radiation field / density). High sensitivity will favor the detection of the far-IR skeletal emission bands of PAHs, which provide specific fingerprints and could lead to the identification of individual PAHs. This overall characterization will allow to use PAH and VSG populations as tracers of physical conditions in spatially resolved protoplanetary disks and nearby galaxies (using mid-IR instruments), and in high redshift galaxies (using the far-IR instrument), thanks to the broad spectral coverage SPICA provides. Based on our previous experience with ISO and Spitzer we discuss how these goals can be reached.

astro-ph.GA↗

arXiv2009

Search for corannulene (C20H10) in the Red Rectangle

Polycyclic Aromatic Hydrocarbons (PAHs) are widely accepted as the carriers of the Aromatic Infrared Bands (AIBs), but an unambiguous identification of any specific interstellar PAH is still missing. For polar PAHs, pure rotational transitions can be used as fingerprints for identification. Combining dedicated experiments, detailed simulations and observations, we explored the mm domain to search for specific rotational transitions of corannulene (C20H10). We performed high-resolution spectroscopic measurements and a simulation of the emission spectrum of UV-excited C20H10 in the environment of the Red Rectangle, calculating its synthetic rotational spectrum. Based on these results, we conducted a first observational campaign at the IRAM 30m telescope towards this source to search for several high-J rotational transitions of (C20H10). The laboratory detection of the J = 112 <- 111 transition of corannulene showed that no centrifugal splitting is present up to this line. Observations with the IRAM 30m telescope towards the Red Rectangle do not show any corannulene emission at any of the observed frequencies, down to a rms noise level of Tmb = 8 mK for the J =135 -> 134 transition at 137.615 GHz. Comparing the noise level with the synthetic spectrum, we are able to estimate an upper limit to the fraction of carbon locked in corannulene of about 1.0x10(-5) relative to the total abundance of carbon in PAHs. The sensitivity achieved shows that radio spectroscopy can be a powerful tool to search for polar PAHs. We compare this upper limit with models for the PAH size distribution, emphasising that small PAHs are much less abundant than predicted. We show that this cannot be explained by destruction but is more likely related to the chemistry of their formation in the environment of the Red Rectangle.

astro-ph.GA↗

arXiv2009

Laboratory studies of polycyclic aromatic hydrocarbons: the search for interstellar candidates

Polycyclic Aromatic Hydrocarbons (PAHs) are considered as a major constituent of interstellar dust. They have been proposed as the carriers of the Aromatic Infrared Bands (AIBs) observed in emission in the mid-IR. They likely have a significant contribution to various features of the extinction curve such as the 220 nm bump,the far-UV rise and the diffuse interstellar bands. Emission bands are also expected in the far-IR, which are better fingerprints of molecular identity than the AIBs. They will be searched for with the Herschel Space Observatory. Rotational emission is also expected in the mm range for those molecules which carry significant dipole moments. Despite spectroscopic studies in the laboratory, no individual PAH species could be identified. This emphasises the need for an investigation on where interstellar PAHs come from and how they evolve due to environmental conditions: ionisation and dissociation upon UV irradiation, interactions with electrons, gas and dust. There is also evidence for PAH species to contribute to the depletion of heavy atoms from the gas phase, in particular Si and Fe. This paper illustrates how laboratory work can be inspired from observations. In particular there is a need for understanding the chemical properties of PAHs and PAH-related species, including very small grains, in physical conditions that mimic those found in interstellar space. This motivates a joint effort between astrophysicists, physicists and chemists. Such interdisciplinary studies are currently performed, taking advantage of the PIRENEA set-up, a cold ion trap dedicated to astrochemistry.

astro-ph.GA↗

arXiv2008

Dehydrogenated polycyclic aromatic hydrocarbons and UV bump

Recent calculations have shown that the UV bump at about 217.5 nm in the extinction curve can be explained by a complex mixture of PAHs in several charge states. Other studies proposed that the carriers are a restricted population made of neutral and singly-ionised dehydrogenated coronene molecules (C24Hn, n less than 3), in line with models of the hydrogenation state of interstellar PAHs predicting that medium-sized species are highly dehydrogenated. To assess the observational consequences of the latter hypothesis we have undertaken a systematic study of the electronic spectra of dehydrogenated PAHs. We use our first results to see whether such spectra show strong general trends upon dehydrogenation. We used state-of-the-art techniques in the framework of the density functional theory (DFT) to obtain the electronic ground-state geometries, and of the time- dependent DFT to evaluate the electronic excited-state properties. We computed the absorption cross-section of the species C24Hn (n=12,10,8,6,4,2,0) in their neutral and cationic charge-states. Similar calculations were performed for other PAHs and their fullydehydrogenated counterparts. pi electron energies are always found to be strongly affected by dehydrogenation. In all cases we examined, progressive dehydrogenation translates into a correspondingly progressive blue shift of the main electronic transitions. In particular, the pi-pi* collective resonance becomes broader and bluer with dehydrogenation. Its calculated energy position is therefore predicted to fall in the gap between the UV bump and the far-UV rise of the extinction curve. Since this effect appears to be systematic, it poses a tight observational limit on the column density of strongly dehydrogenated medium-sized PAHs.

astro-ph↗

arXiv2008

The role of the charge state of PAHs in ultraviolet extinction

Aims: We explore the relation between charge state of polycyclic aromatic hydrocarbons (PAHs) and extinction curve morphology. Methods: We fit extinction curves with a dust model including core-mantle spherical particles of mixed chemical composition (silicate core, $sp^2$ and $sp^3$ carbonaceous layers), and an additional molecular component. We use exact methods to calculate the extinction due to classical particles and accurate computed absorption spectra of PAHs in different charge states, for the contribution due to the molecular component, along a sample of five rather different lines of sight. Results: A combination of classical dust particles and mixtures of real PAHs satisfactorily matches the observed interstellar extinction curves. Variations of the spectral properties of PAHs in different charge states produce changes consistent with the varying relative strengths of the bump and non-linear far-UV rise.

astro-ph↗

arXiv2007

Field Camera Unit for WSO-UV: Phase A Study Report

World Space Observatory UltraViolet (WSO-UV) is a multipurpose space observatory, made by a 170 cm aperture telescope, capable of UV high-resolution spectroscopy, long slit low-resolution spectroscopy, and deep UV and optical imaging. With a nominal mission life time of 5 years, and a planned extension to 10 years, from a geosynchronous orbit with an inclination of 51.8 degrees, WSO-UV will provide observations of exceptional importance for the study of many unsolved astrophysical problems. WSO-UV is implemented in the framework of a collaboration between Russia (chair), China, Germany, Italy, Spain, and Ukraine. This book illustrates the results of the feasibility study for the Field Camera Unit (FCU), a multi-spectral radial instrument on the focal plane of WSO-UV. The book provides an overview of the key science topics that are drivers to the participation of the Italian astronomical community in the WSO-UV project. The science drivers here illustrated have been used to define the technical requirements for the conceptual and architectural design of the Field Camera Unit (FCU) focal plane instrument. In Chapter I we show that WSO-UV will give a significant contribution to solve the key astronomical problems individuated by the ASTRONET consortium, and which are driving the European Space Agency Cosmic Vision program. Chapter II elucidates the scientific requirements for WSO-UV FCU instrument, discussed in Chapter I, which are translated in a list of verifiable top level requirements usable to make the conceptual design of the FCU instrument. Chapter III is dedicated to the Field Camera Unit opto-mechanical design, its detectors and electronics subsystems. Finally, Chapter IV outlines the AIV and GSE plans and activities for the FCU instrument.

astro-ph↗

arXiv2007

Time-dependent density functional study of the electronic spectra of oligoacenes in the charge states -1, 0, +1, and +2

We present a systematic theoretical study of the five smallest oligoacenes (naphthalene, anthracene, tetracene, pentacene, and hexacene) in their anionic,neutral, cationic, and dicationic charge states. We used density functional theory (DFT) to obtain the ground-state optimised geometries, and time-dependent DFT (TD-DFT) to evaluate the electronic absorption spectra. Total-energy differences enabled us to evaluate the electron affinities and first and second ionisation energies, the quasiparticle correction to the HOMO-LUMO energy gap and an estimate of the excitonic effects in the neutral molecules. Electronic absorption spectra have been computed by combining two different implementations of TD-DFT: the frequency-space method to study general trends as a function of charge-state and molecular size for the lowest-lying in-plane long-polarised and short-polarised $π\toπ^\star$ electronic transitions, and the real-time propagation scheme to obtain the whole photo-absorption cross-section up to the far-UV. Doubly-ionised PAHs are found to display strong electronic transitions of $π\toπ^\star$ character in the near-IR, visible, and near-UV spectral ranges, like their singly-charged counterparts. While, as expected, the broad plasmon-like structure with its maximum at about 17-18 eV is relatively insensitive to the charge-state of the molecule, a systematic decrease with increasing positive charge of the absorption cross-section between about 6 and about 12 eV is observed for each member of the class.

physics.chem-ph↗

arXiv2007

On-line database of the spectral properties of polycyclic aromatic hydrocarbons

We present an on-line database of computed molecular properties for a large sample of polycyclic aromatic hydrocarbons (PAHs) in four charge states: -1, 0, +1, and +2. At present our database includes 40 molecules ranging in size from naphthalene and azulene (C10H8) up to circumovalene (C66H20). We performed our calculations in the framework of the density functional theory (DFT) and the time-dependent DFT to obtain the most relevant molecular parameters needed for astrophysical applications. For each molecule in the sample, our database presents in a uniform way the energetic, rotational, vibrational, and electronic properties. It is freely accessible on the web at http://astrochemistry.ca.astro.it/database/ and http://www.cesr.fr/~joblin/database/.

astro-ph↗

arXiv2006

Theoretical evaluation of PAH dications properties

Aims. We present a systematic theoretical study on 40 polycyclic aromatic hydrocarbons dications (PAHs++) containing up to 66 carbon atoms. Methods. We performed our calculations using well established quantum-chemical techniques in the framework of the density functional theory (DFT) to obtain the electronic ground-state properties, and of the time-dependent DFT (TD-DFT) to evaluate the excited\textendash state properties. Results. For each PAH++ considered we computed the absolute visible-UV photo-absorption cross-section up to about 30 eV. We also evaluated their vibrational properties and compared them to those of the corresponding neutral and singly-ionised species. We estimated the adiabatic and vertical second ionisation energy DeltaI through total energy differences. Conclusions. The DeltaI values obtained fall in the energy range 8-13 eV, confirming that PAHs could reach the doubly-ionised state in HI regions. The total integrated IR absorption cross-sections show a marked increase upon ionization, being on the average about two and five times larger for PAHs++ than for PAHs+ and PAHs, respectively. The visible-UV photo-absorption cross-sections for the 0, +1 and +2 charge-states show comparable features but PAHs++ are found to absorb slightly less than their parent neutrals and singly ionized species between ~7 and ~12 eV. Combining these pieces of information we found that PAHs++ should actually be more stable against photodissociation than PAHs and PAHs+,_if_ dissociation tresholds are nearly unchanged by ionization.

astro-ph↗

arXiv2006

A general model for the identification of specific PAHs in the far-IR

Context. In the framework of the interstellar PAH hypothesis, far-IR skeletal bands are expected to be a fingerprint of single species in this class. Aims. A detailed model of the photophysics of interstellar PAHs is required for such single-molecule identification of their far-IR features in the presently available Infrared Space Observatory data and in those of the forthcoming Herschel Space Observatory mission. Methods. We modelled the detailed photophysics of a vast sample of species in different radiation fields, using a compendium of Monte-Carlo techniques and quantum-chemical calculations. This enabled us to validate the use of purely theoretical data and assess the expected accuracy and reliability of the resulting synthetic far-IR emission spectra. Results. We produce positions and intensities of the expected far-IR features which ought to be emitted by each species in the sample in the considered radiation fields. A composite emission spectrum for our sample is computed for one of the most favourable sources for detection, namely the Red Rectangle nebula. The resulting spectrum is compared with the estimated dust emission in the same source, to assess the dependence of detectability on key molecular parameters. Conclusions. Identifying specific PAHs from their far-IR features is going to be a difficult feat in general, still it may well be possible under favourable conditions.

astro-ph↗

arXiv2006

Diagnostics for specific PAHs in the far-IR: searching neutral naphthalene and anthracene in the Red Rectangle

Context. In the framework of the interstellar polycyclic aromatic hydrocarbons (PAHs) hypothesis, far-IR skeletal bands are expected to be a fingerprint of single species in this class. Aims. We address the question of detectability of low energy PAH vibrational bands, with respect to spectral contrast and intensity ratio with ``classical'' Aromatic Infrared Bands (AIBs). Methods. We extend our extablished Monte-Carlo model of the photophysics of specific PAHs in astronomical environments, to include rotational and anharmonic band structure. The required molecular parameters were calculated in the framework of the Density Functional Theory. Results. We calculate the detailed spectral profiles of three low-energy vibrational bands of neutral naphthalene, and four low-energy vibrational bands of neutral anthracene. They are used to establish detectability constraints based on intensity ratios with ``classical'' AIBs. A general procedure is suggested to select promising diagnostics, and tested on available Infrared Space Observatory data for the Red Rectangle nebula. Conclusions. The search for single, specific PAHs in the far-IR is a challenging, but promising task, especially in view of the forthcoming launch of the Herschel Space Observatory.

astro-ph↗