arXiv subjects

K. -J. Chuang

Publications and source records attributed to K. -J. Chuang.

At least 19 recordsLinked to original sources

arXiv2026

In situ characterization of volatile and refractory hydrocarbons produced by UV photolysis of interstellar C$_2$H$_2$ ice

Acetylene (C$_2$H$_2$) is commonly observed in star-forming regions, young stellar objects, and the Solar System. Laboratory and theoretical studies have linked this simplest alkyne to volatile hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) through UV- or cosmic-ray-driven chemistry, but it remains unclear whether refractory material can efficiently form through solid-state reactions of C$_2$H$_2$ on dust grains. We experimentally investigate the chemical complexity induced by UV irradiation of pure C$_2$H$_2$ ice and characterize both volatile and nonvolatile photoproducts. Experiments were performed with MATRI$^2$CES under ultra-high-vacuum conditions at 15 K using 7.2--10.2 eV photons. UV-processed ices were monitored in situ by laser desorption post-ionization reflection time-of-flight mass spectrometry (LDPI ReTOF-MS) combined with pulsed ion deflection (PID). Volatile and refractory products were measured in situ at 15 and 300 K, respectively. After a fluence of $3 \times 10^{17}$ photons cm$^{-2}$, corresponding to about $10^6$ years in dense clouds, large saturated and unsaturated hydrocarbons containing up to 13 carbon atoms are formed. After sublimation of the volatile products, the 300 K residue shows a rich and distinct mass spectrum consistent with refractory material containing conjugated triple (-C$\equiv$C-) and double (-C=C-) bonds. These results demonstrate that UV processing of pure C$_2$H$_2$ ice can produce substantial molecular complexity and refractory hydrocarbons under astronomically relevant conditions, with possible implications for unidentified infrared emission bands.

astro-ph.GA↗

arXiv2026

Quantifying the temperature-dependent yields of N$_2$ and N$_2$H$_4$ formation in vacuum-ultraviolet-irradiated NH$_3$ ice

Gas--grain astrochemical models predict that a substantial fraction of elemental nitrogen in dense cores and protoplanetary disks is locked in molecular nitrogen (N$_2$), in the gas or ice phase, although interstellar N$_2$ ice has not been directly identified. Rosetta measurements at comet 67P/Churyumov--Gerasimenko showed strong N$_2$ depletion relative to CO, while NH$_3$ was the dominant detected nitrogen-bearing ice. We experimentally quantify the conversion of NH$_3$ ice into N$_2$ and N$_2$H$_4$ under astronomically relevant conditions by studying its temperature- and fluence-dependent VUV photochemistry. Experiments were performed under ultra-high vacuum using 40-monolayer NH$_3$ ice at 15, 25, and 70 K irradiated at 115--170 nm to a total fluence of $3.8\times10^{18}$ photons cm$^{-2}$. Laser desorption with post-ionization reflection time-of-flight mass spectrometry (ReTOF-MS) was used to monitor N$_2$ and N$_2$H$_4$ simultaneously. VUV photolysis efficiently forms both products, with formation kinetics and product ratios depending on temperature and photon fluence. Initial-growth fits gave the highest apparent ice-retained N$_2$ formation yield at 15 K, approximately an order of magnitude above those at 25 and 70 K. The N$_2$/NH$_3$ column-density ratio was determined as a function of fluence and compared with astronomical constraints. These results suggest that NH$_3$ ice photochemistry may provide an additional pathway to N$_2$ ice in cold outer planetary environments.

astro-ph.IM↗

arXiv2026

Pulsed ion deflection to overcome detector saturation in cryogenic ice sampling

In 2014, we introduced a new experimental approach to study the UV photo-processing of cryogenic ices of astrophysical interest using laser ablation in combination with ionization and time-of-flight mass spectrometry (ToF-MS). The setup, MATRI$^2$CES (Mass Analytical Tool to Research Interstellar ICES), allowed us to detect newly formed species at low abundances. However, we found that with increasing molecular complexity, the detection of larger photoproducts was hindered by the dynamic range of the detector. Here, we introduce a method to overcome this issue that we expect to be useful for similar applications in other research fields. The concept is based on a precisely controlled high-energy pulser that regulates the voltage across the deflection plates of the ToF-MS to deflect the most abundant species and prevent them from reaching the detector. In this way, the detector sensitivity can be increased from an operating voltage of 2500~V up to 3000~V. The applicability is first illustrated using an argon matrix, in which $^{40}$Ar$^+$ ions are deflected to increase the detection sensitivity for $^{40}$Ar$^{2+}$ at $m/z=20$ and $^{40}$Ar$_2^+$ at $m/z=80$ by a factor of 30. Similarly, we show that substantially larger complex organic molecules can be measured in UV-irradiated methanol ice.

astro-ph.IM↗

arXiv2025

UV irradiation of ethanol-containing interstellar ice analogs: Photostability in CH3CH2OH:CO mixtures

Ethanol (CH3CH2OH) has been detected in interstellar ices within regions associated with the early stages of star and planet formation. Its solid-phase pathways can lead to diverse conditions that can significantly influence its photostability and -chemistry. Laboratory studies have explored the effects of energetic processing on pure ethanol ices, there is a gap in understanding how ethanol behaves in astrophysically relevant mixed ices. This proof-of-principle study aims to quantify how the ice composition influences the photostability of ethanol mixed with CO, from both physical and chemical perspectives. It also seeks to highlight the importance of balancing constructive and destructive processes. Mixtures with ethanol to CO ratios ranging from 1:0 to 1:11 are exposed to UV irradiation from a microwave discharge H lamp under UHV conditions, at 16 K. The evolution of the solid phase is tracked using reflection-absorption infrared spectroscopy, and changes in the gas phase are monitored with a quadrupole mass spectrometer. Temperature-programmed desorption experiments aid in the identification of infrared spectral features. A radiative-transfer model has been developed to account for the influence of ice composition on the effective photon flux. The model reveals that, during later stages of irradiation, photoproducts play a significant role in the absorbing of incident photons, highlighting the complex cascade of processes initiated by single-photon absorption in ethanol-containing ices. By evaluating photodestruction cross sections as a function of the initial ice composition, we found that CO exerts a stabilizing effect on ethanol. For highly dilute ethanol:CO mixtures, representative of astronomical ices, the photodestruction cross section of ethanol is estimated to ~1.6E-17 cm2/photon after correcting for the effective absorbed UV fluence of the studied interstellar ice analogs.

astro-ph.GA↗

arXiv2025

Production of linear alkanes via the solid-state hydrogenation of interstellar polyynes

Highly unsaturated carbon chains, including polyynes, have been detected in many astronomical regions and planetary systems. With the success of the QUIJOTE survey of the TMC-1, the community has seen a "boom" in the number of detected carbon chains. On the other hand, the Rosetta mission revealed the release of fully saturated hydrocarbons, C$_3$H$_8$, C$_4$H$_{10}$, C$_5$H$_{12}$, and (under specific conditions) C$_6$H$_{14}$ with C$_7$H$_{16}$, from the comet 67P/Churyumov-Gerasimenko. The detection of the latter two is attributed to dust-rich events. Similarly, the analysis of samples returned from asteroid Ryugu by Hayabusa2 mission indicates the presence of long saturated aliphatic chains in Ryugu's organic matter. The surface chemistry of unsaturated carbon chains under conditions resembling those of molecular clouds can provide a possible link among these independent observations. However, laboratory-based investigations to validate such a chemistry is still lacking. In the present study, we aim to experimentally verify the formation of fully saturated hydrocarbons by the surface hydrogenation of C$_{2n}$H$_2$ ($n>1$) polyynes under ultra-high vacuum conditions at 10 K. We undertook a two-step experimental technique. First, a thin layer of C$_2$H$_2$ ice was irradiated by UV-photons ($\geq$ 121 nm) to achieve a partial conversion of C$_2$H$_2$ into larger polyynes: C$_4$H$_2$ and C$_6$H$_2$. Afterwards, the obtained photoprocessed ice was exposed to H atoms to verify the formation of various saturated hydrocarbons. In addition to C$_2$H$_6$, which was investigated previously, the formation of larger alkanes, including C$_4$H$_{10}$ and (tentatively) C$_6$H$_{14}$, is confirmed by our study. A qualitative analysis of the obtained kinetic data indicates that hydrogenation of HCCH and HCCCCH triple bonds proceeds at comparable rates, given a surface temperature of 10 K.}

astro-ph.EP↗

arXiv2024

Formation of N-bearing complex organic molecules in molecular clouds: Ketenimine, acetonitrile, acetaldimine, and vinylamine via the UV photolysis of C$_2$H$_2$ ice

The solid-state C$_2$H$_2$ chemistry in interstellar H$_2$O-rich ice has been proposed to explain astronomically observed complex organic molecules (COMs), including ketene (CH$_2$CO), acetaldehyde (CH$_3$CHO), and ethanol (CH$_3$CH$_2$OH), toward early star-forming regions. This formation mechanism is supported by recent laboratory studies and theoretical calculations for the reactions of C$_2$H$_2$+OH/H. However, the analog reaction of C$_2$H$_2$+NH$_2$ forming N-bearing species has been suggested to have a relatively low rate constant that is orders of magnitude lower than the value of C$_2$H$_2$+OH. This work extends our previous laboratory studies on O-bearing COM formation to investigate the interactions between C$_2$H$_2$ and NH$_3$ ice triggered by cosmic ray-induced secondary UV photons under molecular cloud conditions. Experiments were performed in an ultra-high vacuum chamber to investigate the UV photolysis of the C$_2$H$_2$:NH$_3$ ice mixture at 10 K. The studied ice chemistry of C$_2$H$_2$ with NH$_2$ radicals and H atoms resulting from the UV photodissociation of NH$_3$ leads to the formation of several N-bearing COMs, including vinylamine (CH$_2$CHNH$_2$), acetaldimine (CH$_3$CHNH), acetonitrile (CH$_3$CN), ketenimine (CH$_2$CNH), and tentatively ethylamine (CH$_3$CH$_2$NH$_2$). The experimental results show an immediate and abundant CH$_2$CHNH$_2$ yield as the first-generation product, which is further converted into other chemical derivatives. The effective destruction and formation cross-section values of parent species and COMs were derived, and we discuss the chemical links among these molecules and their astronomical relevance.

astro-ph.GA↗

arXiv2024

A deep search for large complex organic species toward IRAS16293-2422 B at 3 mm with ALMA

Complex organic molecules (COMs) have been detected ubiquitously in protostellar systems. However, at shorter wavelengths (~0.8mm) it is more difficult to detect larger molecules than at longer wavelengths (~3mm) because of the increase of millimeter dust opacity, line confusion, and unfavorable partition function. We aim to search for large molecules (>8 atoms) in the ALMA Band 3 spectrum of IRAS 16293-2422 B. We search for more than 70 molecules and identify as many lines as possible in the spectrum. The spectral settings were set to specifically target three-carbon species such as propanol and glycerol. We identify lines of 31 molecules including many oxygen-bearing COMs such as CH3OH and c-C2H4O and a few nitrogen- and sulfur-bearing ones such as HOCH2CN and CH3SH. The largest detected molecules are gGg-(CH2OH)2 and CH3COCH3. We do not detect glycerol or propanol but provide upper limits for them which are in line with previous laboratory and observational studies. The line density in Band 3 is only ~2.5 times lower in frequency space than in Band 7. From the detected lines in Band 3 at a $\gtrsim 6σ$ level, ~25-30% of them could not be identified indicating the need for more laboratory data of rotational spectra. We find similar column densities and column density ratios of COMs (within a factor ~2) between Band 3 and Band 7. The effect of dust optical depth for IRAS 16293-2422 B at an off-source location on column densities and column density ratios is minimal. Moreover, for warm protostars, long wavelength spectra are not only crowded, but also take longer integration times to reach the same sensitivity limit. The 3mm search has not yet resulted in detection of larger and more complex molecules in warm sources. A full deep ALMA Band 2-3 (i.e., 3-4 mm) survey is needed to assess whether low frequency data have the potential to reveal more complex molecules in warm sources.

astro-ph.GA↗

arXiv2023

Interstellar carbonaceous dust erosion induced by X-ray irradiation of water ice in star-forming regions

The chemical inventory of protoplanetary midplanes is the basis for forming planetesimals. Among them, solid-state reactions based on CO/CO$_2$ toward molecular complexity on interstellar dust grains have been studied in theoretical and laboratory work. In this work, the erosion of C dust grains induced by X-ray irradiation of H$_2$O ice was systematically investigated for the first time. The work aims to provide a better understanding of the reaction mechanism using selectively isotope-labeled oxygen/carbon species in kinetic analysis. Ultrahigh vacuum experiments were performed to study the interstellar ice analog on sub-$μ$m thick C dust at $\sim$13~K. H$_2$O or O$_2$ ice was deposited on the pre-synthesized amorphous C dust and exposed to soft X-ray photons (250--1250~eV). Fourier-transform infrared spectroscopy was used to monitor in situ the newly formed species as a function of the incident photon fluence. Field emission scanning electron microscopy was used to monitor the morphological changes of (non-)eroded carbon samples. The X-ray processing of the ice/dust interface leads to the formation of CO$_2$, which further dissociates and forms CO. Carbonyl groups are formed by oxygen addition to grain surfaces and are confirmed as intermediate species in the formation process. The yields of CO and CO$_2$ were found to be dependent on the thickness of the carbon layer. The astronomical relevance of the experimental findings is discussed.

astro-ph.SR↗

arXiv2023

CoCCoA: Complex Chemistry in hot Cores with ALMA. Selected oxygen-bearing species

Complex organic molecules (COMs) have been observed to be abundant in the gas phase toward protostars. Deep line surveys have been carried out only for a limited number of well-known high-mass star forming regions using the Atacama Large Millimeter/submillimeter Array (ALMA), which has unprecedented resolution and sensitivity. Statistical studies on oxygen-bearing COMs (O-COMs) in high-mass protostars using ALMA are still lacking. With the recent CoCCoA survey, we are able to determine the column density ratios of six O-COMs with respect to methanol (CH$_3$OH) in a sample of 14 high-mass protostellar sources to investigate their origin through ice and/or gas-phase chemistry. The selected species are: acetaldehyde (CH$_3$CHO), ethanol (C$_2$H$_5$OH), dimethyl ether (DME, CH$_3$OCH$_3$), methyl formate (MF, CH$_3$OCHO), glycolaldehyde (GA, CH$_2$OHCHO), and ethylene glycol (EG, (CH$_2$OH)$_2$). DME and MF have the highest and most constant ratios within one order of magnitude, while the other four species have lower ratios and exhibit larger scatter by 1-2 orders of magnitude. We compare the O-COM ratios of high-mass CoCCoA sources with those of 5 low-mass protostars available from the literature, along with the results from experiments and simulations. We find that the O-COM ratios with respect to methanol are on the same level in both the high- and low-mass samples, which suggests that these species are mainly formed in similar environments during star formation, probably in ice mantles on dust grains during early pre-stellar stages. Current simulations and experiments can reproduce most observational trends with a few exceptions, and hypotheses exist to explain the differences between observations and simulations/experiments, such as the involvement of gas-phase chemistry and different emitting areas of molecules.

astro-ph.GA↗

arXiv2023

Resonant infrared irradiation of CO and CH3OH interstellar ices

Solid-phase photo-processes involving icy dust grains greatly affect the chemical evolution of the interstellar medium by leading to the formation of complex organic molecules and by inducing photodesorption. So far, the focus of laboratory studies has been mainly on the impact of energetic ultraviolet (UV) photons on ices, but direct vibrational excitation by infrared (IR) photons is expected to influence the morphology and content of interstellar ices as well. However, little is still known about the mechanisms through which this excess vibrational energy is dissipated, and its implications on the structure and ice photochemistry. In this work, we present a systematic investigation of the behavior of interstellar relevant CO and CH3OH ice analogues upon resonant excitation of vibrational modes using tunable infrared radiation, leading to both the quantification of infrared-induced photodesorption and insights in the impact of vibrational energy dissipation on ice morphology. We utilize an ultrahigh vacuum setup at cryogenic temperatures to grow pure CO and CH3OH ices, as well as mixtures of the two. We expose the ices to intense, near-monochromatic mid-infrared free-electron-laser radiation to selectively excite the species. The dissipation of vibrational energy is observed to be highly dependent on the excited mode and the chemical environment of the ice. All amorphous ices undergo some degree of restructuring towards a more organized configuration upon on-resonance irradiation. Moreover, IR-induced photodesorption is observed to occur for both pure CO and CH3OH ices, with interstellar photodesorption efficiencies of the order of 10 molecules cm-2 s-1 (i.e., comparable to or higher than UV-induced counterparts). Indirect photodesorption of CO upon vibrational excitation of CH3OH in ice mixtures is also observed to occur, particularly in environments rich in methanol.

astro-ph.GA↗

arXiv2022

Formation of the simplest amide in molecular clouds: formamide (NH$_{2}$CHO) and its derivatives in H$_2$O-rich and CO-rich interstellar ice analogs upon VUV irradiation

The astronomical detection of formamide (NH$_2$CHO) toward various star-forming regions and in cometary material implies that the simplest amide might have an early origin in dark molecular clouds at low temperatures. Laboratory studies have proven the efficient NH$_2$CHO formation in interstellar CO:NH$_3$ ice analogs upon energetic processing. However, it is still under debate, whether the proposed radical-radical recombination reactions forming complex organic molecules remain valid in an abundant H$_2$O environment. The aim of this work was to investigate the formation of NH$_2$CHO in H$_2$O- and CO-rich ices under conditions prevailing in molecular clouds. Therefore, different ice mixtures composed of H$_2$O:CO:NH$_3$ (10:5:1), CO:NH$_3$ (4:1), and CO:NH$_3$ (0.6:1) were exposed to vacuum ultraviolet photons in an ultra-high vacuum chamber at 10 K. Fourier-transform infrared spectroscopy was utilized to monitor in situ the initial and newly formed species as a function of photon fluence. The infrared spectral identifications are complementarily secured by a temperature-programmed desorption experiment combined with a quadrupole mass spectrometer. The energetic processing of CO:NH$_3$ ice mixtures mainly leads to the NH$_2$CHO formation, along with its chemical derivatives such as isocyanic acid (HNCO) and cyanate ion (OCN$^-$). The formation kinetics of NH$_2$CHO shows an explicit dependency on ice ratios and compositions; the highest yield is found in H$_2$O-rich ice. The astronomical relevance of the resulting reaction network is discussed.

astro-ph.GA↗

arXiv2022

A pathway to peptides in space through the condensation of atomic carbon

Organic molecules are widely present in the dense interstellar medium, and many have been synthesized in the laboratory on Earth under the conditions typical for an interstellar environment. Until now, however, only relatively small molecules of biological interest have been demonstrated to form experimentally under typical space conditions. Here we prove experimentally that the condensation of carbon atoms on the surface of cold solid particles (cosmic dust) leads to the formation of isomeric polyglycine monomers (aminoketene molecules). Following encounters between aminoketene molecules, they polymerize to produce peptides of different lengths. The chemistry involves three of the most abundant species (CO, C and NH$_3$) present in star-forming molecular clouds, and proceeds via a novel pathway that skips the stage of amino acid formation in protein synthesis. The process is efficient, even at low temperatures, without irradiation or the presence of water. The delivery of biopolymers formed by this chemistry to rocky planets in the habitable zone might be an important element in the origins of life.

physics.bio-ph↗

arXiv2021

Formation of complex organic molecules in molecular clouds: acetaldehyde, vinyl alcohol, ketene, and ethanol via the "energetic" processing of C$_2$H$_2$ ice

The simultaneous detection of organic molecules of the form C$_2$H$_{\text{n}}$O, such as ketene (CH$_2$CO), acetaldehyde (CH$_3$CHO), and ethanol (CH$_3$CH$_2$OH), toward early star-forming regions offers hints of shared chemical history. Several reaction routes have been proposed and experimentally verified under various interstellar conditions to explain the formation pathways involved. Most noticeably, the non-energetic processing of C$_2$H$_2$ ice with OH-radicals and H-atoms was shown to provide formation routes to ketene, acetaldehyde, ethanol, and vinyl alcohol (CH$_2$CHOH) along the H$_2$O formation sequence on grain surfaces. In this work, the non-energetic formation scheme is extended with laboratory measurements focusing on the energetic counterpart, induced by cosmic rays penetrating the H$_2$O-rich ice mantle. The focus here is on the H$^+$ radiolysis of interstellar C$_2$H$_2$:H$_2$O ice analogs at 17 K. Ultra-high vacuum experiments were performed to investigate the 200 keV H$^+$ radiolysis chemistry of predeposited C$_2$H$_2$:H$_2$O ices, both as mixed and layered geometries. Fourier-transform infrared spectroscopy was used to monitor in situ newly formed species as a function of the accumulated energy dose (or H$^+$ fluence). The infrared (IR) spectral assignments are further confirmed in isotope labeling experiments using H$_2$$^{18}$O. The energetic processing of C$_2$H$_2$:H$_2$O ice not only results in the formation of (semi-) saturated hydrocarbons (C$_2$H$_4$ and C$_2$H$_6$) and polyynes as well as cumulenes (C$_4$H$_2$ and C$_4$H$_4$), but it also efficiently forms O-bearing COMs, including vinyl alcohol, ketene, acetaldehyde, and ethanol, for which the reaction cross-section and product composition are derived. A clear composition transition of the product, from H-poor to H-rich species, is observed as a function of the accumulated energy dose.

astro-ph.GA↗

arXiv2020

A non-energetic mechanism for glycine formation in the interstellar medium

The detection of the amino acid glycine and its amine precursor methylamine on the comet 67P/Churyumov-Gerasimenko by the Rosetta mission provides strong evidence for a cosmic origin of prebiotics on Earth. How and when such complex organic molecules form along the process of star- and planet-formation remains debated. We report the first laboratory detection of glycine formed in the solid phase through atom and radical-radical addition surface reactions under cold dense interstellar cloud conditions. Our experiments, supported by astrochemical models, suggest that glycine forms without the need for energetic irradiation, such as UV photons and cosmic rays, in interstellar water-rich ices, where it remains preserved, in a much earlier star-formation stage than previously assumed. We also confirm that solid methylamine is an important side-reaction product. A prestellar formation of glycine on ice grains provides the basis for a complex and ubiquitous prebiotic chemistry in space enriching the chemical content of planet-forming material.

astro-ph.IM↗

arXiv2020

A cryogenic ice setup to simulate carbon atom reactions in interstellar ices

The design, implementation, and performance of a customized carbon atom beam source for the purpose of investigating solid-state reaction routes in interstellar ices in molecular clouds are discussed. The source is integrated into an existing ultrahigh vacuum setup, SURFace REaction SImulation DEvice (SURFRESIDE$^{2}$), which extends this double atom (H/D, O, and N) beamline apparatus with a third atom (C) beamline to a unique system that is fully suited to explore complex organic molecule solid-state formation under representative interstellar cloud conditions. The parameter space for this system is discussed, which includes the flux of the carbon atoms hitting the ice sample, their temperature, and the potential impact of temperature on ice reactions. Much effort has been put into constraining the beam size to within the limits of the sample size with the aim to reduce carbon pollution inside the setup. How the C-atom beam performs is quantitatively studied through the example experiment, C + $^{18}$O$_2$, and supported by computationally-derived activation barriers. The potential for this source to study the solid-state formation of interstellar complex organic molecules through C-atom reactions is discussed.

astro-ph.SR↗

arXiv2020

An experimental study of the surface formation of methane in interstellar molecular clouds

Methane is one of the simplest stable molecules that is both abundant and widely distributed across space. It is thought to have partial origin from interstellar molecular clouds, which are near the beginning of the star formation cycle. Observational surveys of CH$_4$ ice towards low- and high-mass young stellar objects showed that much of the CH$_4$ is expected to be formed by the hydrogenation of C on dust grains, and that CH$_4$ ice is strongly correlated with solid H$_2$O. Yet, this has not been investigated under controlled laboratory conditions, as carbon-atom chemistry of interstellar ice analogues has not been experimentally realized. In this study, we successfully demonstrate with a C-atom beam implemented in an ultrahigh vacuum apparatus the formation of CH$_4$ ice in two separate co-deposition experiments: C + H on a 10 K surface to mimic CH$_4$ formation right before H$_2$O ice is formed on the dust grain, and C + H + H$_2$O on a 10 K surface to mimic CH$_4$ formed simultaneously with H$_2$O ice. We confirm that CH$_4$ can be formed by the reaction of atomic C and H, and that the CH$_4$ formation rate is 2 times greater when CH$_4$ is formed within a H$_2$O-rich ice. This is in agreement with the observational finding that interstellar CH$_4$ and H$_2$O form together in the polar ice phase, i.e., when C- and H-atoms simultaneously accrete with O-atoms on dust grains. For the first time, the conditions that lead to interstellar CH$_4$ (and CD$_4$) ice formation are reported, and can be incorporated into astrochemical models to further constrain CH$_4$ chemistry in the interstellar medium and in other regions where CH$_4$ is inherited.

astro-ph.SR↗

arXiv2020

Formation of complex molecules in translucent clouds: Acetaldehyde, vinyl alcohol, ketene, and ethanol via nonenergetic processing of C2H2 ice

Complex organic molecules (COMs) have been identified toward high- and low-mass protostars as well as molecular clouds, suggesting that these interstellar species originate from the early stage(s) of starformation. The reaction pathways resulting in COMs described by the formula C$_2$H$_\text{n}$O are still under debate. In this work, we investigate the laboratory possible solid-state reactions that involve simple hydrocarbons and OH-radicals along with H$_2$O ice under translucent cloud conditions (1$\leq$A$_V$$\leq$5 and \textit{n}$_\text{H}$$\sim$10$^3$ cm$^{-3}$). We focus on the interactions of C$_2$H$_2$ with H-atoms and OH-radicals, which are produced along the H$_2$O formation sequence on grain surfaces at 10 K. Ultra-high vacuum (UHV) experiments were performed to study the surface chemistry observed during C$_2$H$_2$ + O$_2$ + H codeposition, where O$_2$ was used for the in-situ generation of OH-radicals. Reflection absorption infrared spectroscopy (RAIRS) was applied to in situ monitor the initial and newly formed species. After that, a temperature-programmed desorption experiment combined with a Quadrupole mass spectrometer (TPD-QMS) was used as a complementary analytical tool. The investigated 10 K surface chemistry of C$_2$H$_2$ with H-atoms and OH-radicals not only results in semi and fully saturated hydrocarbons, such as ethylene (C$_2$H$_4$) and ethane (C$_2$H$_6$), but it also leads to the formation of COMs, such as vinyl alcohol, acetaldehyde, ketene, ethanol, and possibly acetic acid. It is concluded that OH-radical addition reactions to C$_2$H$_2$, acting as a molecular backbone, followed by isomerization (i.e., keto-enol tautomerization) via an intermolecular pathway and successive hydrogenation provides a so far experimentally unreported solid-state route for the formation of these species without the need of energetic input.

astro-ph.SR↗

arXiv2019

Synthesis of solid-state Complex Organic Molecules through accretion of simple species at low temperatures

Complex organic molecules (COMs) have been detected in the gas-phase in cold and lightless molecular cores. Recent solid-state laboratory experiments have provided strong evidence that COMs can be formed on icy grains through 'non-energetic' processes. In this contribution, we show that propanal and 1-propanol can be formed in this way at the low temperature of 10 K. Propanal has already been detected in space. 1-propanol is an astrobiologically relevant molecule, as it is a primary alcohol, and has not been astronomically detected. Propanal is the major product formed in the C2H2 + CO + H experiment, and 1-propanol is detected in the subsequent propanal + H experiment. The results are published in Qasim et al. (2019c). ALMA observations towards IRAS 16293-2422B are discussed and provide a 1-propanol:propanal upper limit of < 0.35 - 0.55, which are complemented by computationally-derived activation barriers in addition to the performed laboratory experiments.

astro-ph.SR↗