As mentioned previously, matter within most diffuse interstellar clouds is primarily composed of atomic and ionic material, with a significantly smaller number of molecules also being present due to the high rates of photon and cosmic ray induced dissociation and ionization processes. Consequentially, the chemistry within these clouds is dominated by gas-phase reactions including those involving or producing ions. At the edges of the diffuse cloud, where stellar UV radiation is more intense, photo-ionization of carbon atoms produces C⁺, while within the diffuse cloud interior cosmic ray driven chemistry is more dominant and allows for the ionization of H and H₂ (Smith 1992). The formation of H₂ ⁺ in particular is important, as this species is the direct precursor to H₃ ⁺: H 2   +  H 2 +   →  H  +  H 3 +

For a long time, the formation and presence of H₃ ⁺ within diffuse clouds were highly controversial due to its suspected high rate of dissociative recombination mediated by electrons emitted from the photo-ionization of carbon atoms (Larson et al., 2000; Larsson et al., 2008). However, its direct observation in diffuse clouds (McCall et al., 1998) combined with the discovery of a new method of recombination (Kokoouline and Greene 2003) confirmed its presence and role within interstellar chemistry: H₃ ⁺ efficiently donates a proton to other atoms and molecules due to the low proton affinity of H₂. The resultant protonated species is reactive, and is thus capable of triggering various chains of ion-molecule reactions. For instance, the reaction with CO produces HCO⁺, while the reaction with atomic oxygen produces OH⁺: H 3 + +  CO  →  H 2   +  HCO + H 3 +   +  O  →  H 2   +  OH +

OH⁺ may also be formed as a result of a two-step process starting with the charge-transfer reaction between atomic oxygen and H⁺ to yield O⁺, which subsequently reacts with H₂ to furnish OH⁺ (Yamamoto 2017). The formation of OH⁺ is the first step towards the formation of interstellar gas-phase H₂O. The reaction of OH⁺ with one moiety of H₂ yields H₂O⁺, and the reaction with a second moiety produces H₃O⁺ (Larsson et al., 2012). The H₃O⁺ molecular ion is isoelectronic with NH₃ and so is a stable species which resists further reactions with H₂ (Geppert and Larsson 2013). Instead, it undergoes dissociative recombination with electrons to yield either OH (∼60% of outcomes) or H₂O (∼25% of outcomes).

The detections of OH⁺, H₂O⁺, and H₃O⁺ within diffuse interstellar environments have been made using ground- and space-based telescopes working in the THz/F-IR range, such as the Atacama Pathfinder Experiment (APEX) and the HIFI instrument aboard the Herschel Space Observatory (for more detail, refer to Section 2), thus confirming their contribution to chemistry in such settings (Gerin et al., 2010a; Gupta et al., 2010; Wyrowski et al., 2010; Wiesemeyer et al., 2016). A reaction scheme analogous to the formation of H₂O from OH⁺ has also been invoked to explain the formation of HCl within diffuse clouds starting from Cl⁺. Such a reaction scheme has been validated by the detection of the relevant intermediate species HCl⁺ and H₂Cl⁺ by the HIFI instrument (Lis et al., 2010; De Luca et al., 2012).

Reactions leading to the formation of carbon-bearing molecules within diffuse interstellar media are more challenging to explain compared to the oxygen and chlorine chemistry outlined above. Indeed, the formation of CH⁺, one of the earliest known interstellar molecules (Douglas and Herzberg 1941), is still not completely understood and several simulations have underestimated its observed abundance within diffuse clouds (e.g., van Dishoeck and Black 1986; Pan et al., 2004; Godard et al., 2009). It is apparent that the formation of CH⁺ cannot rely on the reaction between H₂ and C⁺ due to the considerable endothermicity of this reaction (Myers et al., 2015; Valdivia et al., 2017; Mosely et al., 2021; Plašil et al., 2021). In light of this, alternative mechanisms have been suggested to account for its presence within the diffuse interstellar medium. For instance, it has been suggested that the radiative association of C⁺ and H₂ to yield CH₂ ⁺ with the concomitant emission of a photon is the first step towards interstellar CH⁺, as the photo-dissociation of the former may lead to the latter (Yamamoto 2017). However, the rate at which radiative association occurs is fairly low (Graff et al., 1983; Barinovs and van Hemert 2006) and indeed the primary reaction pathway of CH₂ ⁺ within diffuse interstellar media is the reaction with H₂ which furnishes CH₃ ⁺. As such, the potential contribution of this reaction network in accounting for interstellar CH⁺ abundances is probably low.

Another proposed formation route for CH⁺ is the direct reaction between C⁺ and H₂ if the endothermicity of the reaction is overcome by some mechanism which causes a localized warming effect which raises the temperature to a few thousand K. Initially, it was thought that this localized warming could be achieved in regions of the diffuse cloud processed by magneto-hydrodynamic shock waves (Elitzur and Watson 1980; Draine and Katz 1986). However, such processes are now thought to be an unlikely source of CH⁺ as the radial velocity for this molecule and for CH have been observed to be similar. Among other ideas, gas heating caused by turbulences within the cloud has also been found to be unsatisfactory in accounting for the observed abundances of CH⁺ (Godard and Cernicharo 2013), as have reactions between C²⁺ and H₂ in X-ray dominated regions of the diffuse cloud (Plašil et al., 2021). Alfvén waves have also been suggested as a potential source of CH⁺ (Federman et al., 1996), however, to the best of the authors’ knowledge, this has been neither corroborated nor firmly rejected. As such, the elusive source of CH⁺ within diffuse interstellar media remains an unanswered question. There thus exists a strong motivation to address this problem, as the formation of CH⁺ may be an important step in the synthesis of significantly more complex carbon-based molecules such as fullerenes and polycyclic aromatic hydrocarbons (PAHs), which are suspected of being the primary carriers of observed diffuse interstellar bands and which may bear relevance to the synthesis of prebiotic molecules (Taylor and Duley 1997).

With regards to molecular detections in diffuse interstellar clouds, a significant number have been made using methods and techniques which exploit the submillimeter, millimeter, and centimeter regions of the electromagnetic spectrum, including THz/F-IR spectroscopy (Snow and McCall 2006; Yamamoto 2017). Indeed, such techniques are the preferred method for detecting polyatomic molecules, as these molecules are difficult to identify using optical spectroscopy (as was done historically) due to the pre-dissociative nature of their excited states. The HIFI instrument aboard the Herschel Space Observatory in particular has proven to be invaluable to the detection and mapping of molecules in diffuse interstellar media, having provided much information on the chemistry of hydrogen-, carbon-, oxygen-, nitrogen-, sulfur-, fluorine-, and chlorine-bearing molecules within diffuse clouds (Gerin et al., 2010a, 2010b, 2012; Neufeld et al., 2010a, 2010b, 2012a; Langer et al., 2010; Persson et al., 2010; Sonnentrucker et al., 2010; Monje et al., 2011, 2013; De Luca et al., 2012; Esplugues et al., 2014; Schilke et al., 2014; Indriolo et al., 2015; Jacob et al., 2020).

Other instruments and telescopes have also aided greatly in the elucidation of the chemical complexity of the diffuse interstellar medium. For example, APEX, the Atacama Large Millimeter/Submillimeter Array (ALMA), and the GREAT instrument aboard the Stratospheric Observatory for Infrared Astronomy (SOFIA) have all been used in the detection of sulfur-bearing molecules, including isotopologues (Menten et al., 2011; Neufeld et al., 2012b, 2015; Muller et al., 2017). Perhaps the most exciting of all has been the series of recent ALMA observations of complex molecules. The work of Thiel et al. (2017), for instance, investigated the presence of prebiotic complex organic molecules within diffuse media and detected several species, including CH₃OH, CH₃CN, CH₃CHO, HC₃N, and CHONH₂. Such results are of immense consequence, as they imply that certain molecular precursors to life either form early on in the astrochemical cycle (Figure 1), or else survive a process of expansion from denser interstellar media.

Condensation of diffuse clouds results in the formation of dense (dark) clouds. During this process, the dominant material is converted from atomic and ionic species to molecular ones. For instance, H₂ becomes the dominant form of hydrogen, while the dominant form of carbon changes sequentially from C⁺, to C, and finally to CO (Snow and Bierbaum 2008; Larsson et al., 2012). As such, these structures have also been appropriately dubbed molecular clouds. In their review, Arumainayagam et al. (2019) highlighted the chemical productivity of dense clouds and identified three milieux for astrochemical reactions within them. The first of these is gas-phase chemistry, which includes radical-radical, radical-neutral, and ion-neutral reactions. The second is chemistry occurring on bare carbonaceous or silicate dust grain surfaces, while the third includes all chemical reactions occurring via energetic and non-energetic processing of icy grain mantles. In this sub-section, we will largely limit ourselves to a brief overview of ion-molecule reactions which occur in the gas-phase within dense interstellar clouds.

Gas-phase ion-neutral reactions within dense interstellar clouds are favorable, barrierless chemical processes. The source of the ionic species within the cloud is somewhat dependent upon the location of the reaction within the cloud structure. Within the densest regions (surrounding the cloud core), ionization of molecules is caused almost exclusively by penetrating galactic cosmic rays. However, within the less dense regions of the clumpy cloud structure, far- and vacuum-UV components of the interstellar radiation field are the primary cause of molecular ionization via photon-induced electron loss processes. Furthermore, in the presence of OB stars, irradiation of molecular material by X-rays may also contribute to the formation of ionic species.

Cosmic ray induced ionization of H₂ leads indirectly to the formation of H₃ ⁺ as was described for diffuse interstellar clouds. The low proton affinity of H₂ allows H₃ ⁺ to be an efficient proton donor to other species (Larsson et al., 2012). For example, the reaction with N₂ yields N₂H⁺, which is frequently used as a tracer for N₂ within interstellar space when observing with radio telescopes, since N₂ does not possess a permanent dipole moment. Ionized hydrogen, primarily in the form of H⁺, readily undergoes reactions with other atoms such as nitrogen atoms. The resultant product NH⁺ may undergo subsequent hydrogenation reactions with H₂ to sequentially form NH₂ ⁺, NH₃ ⁺, and NH₄ ⁺ (Geppert and Larsson 2013). Finally, dissociative recombination with an incident electron efficiently affords gas-phase NH₃ (Öjekull et al., 2004).

Interestingly, the analogous reaction pathway to the formation of gas-phase CH₄ is not thought to be significant within dense clouds. This is because once CH₅ ⁺ is formed, the dominant dissociative recombination mechanism involves the simultaneous loss of two hydrogen atoms, creating CH₃ rather than CH₄ (Semaniak et al., 1998; Viti et al., 2000). The formation of CH₄ and several other carbon-based molecules within the interstellar medium is instead likely to rely on other mechanisms, such as hydrogenation reactions at the surfaces of dust grains (Qasim et al., 2020).

A large number of carbon-based complex organic molecules are known to exist within dense clouds. Until recently, it was thought that these molecules formed within the solid phase in icy grain mantles and were released into the gas phase upon thermal or photo-desorption. However, a growing body of literature has documented the presence of such gas-phase complex organic molecules within starless and pre-stellar cores, where such desorption processes do not take place. Scibelli and Shirley (2020), for instance, have detected CH₃OH and CH₃CHO in several such environments and have suggested that the radicals and molecules responsible for the formation of these species may be formed in the ice phase. The release of energy upon their formation allows them to sublimate into the gas phase (a process termed reactive desorption) whereupon they react to form these product molecules.

Another region of dense clouds which may host a rich gas-phase chemistry leading to the formation of complex organic molecules is the edge of the cloud: the photo-dissociation region (PDR). In this region, the cloud interacts with the intense UV components of the interstellar radiation field resulting in the desorption of solid-phase molecules and an increase in the occurrence of gas-phase processes. Using the IRAM 30 m telescope, Cuadrado et al. (2017) were able to perform a millimeter line survey towards the edge of the Orion Bar PDR and successfully detected a plethora of complex molecules including carboxylic acids, aldehydes, alkenes, and sulfur-containing molecules. Soma et al. (2018) reported similar results. The production and survival of complex molecules in such an environment is significant from the perspective of astrobiology and, although their exact formation mechanisms are still not completely understood, it is likely that a non-negligible contribution comes from gas-phase reactions.

Of course, other processes leading to the formation of complex organic molecules within dense interstellar clouds are also known. Garrod et al. (2008), for instance, demonstrated that the warm up of icy grain mantles previously processed by galactic cosmic rays under cold conditions yielded various complex organic molecules in abundances which matched those documented observationally, while Balucani et al. (2015) invoked radiative association as a gas-phase process leading to their formation. An interesting mechanism which has been suggested to account for the formation of complex organic molecules is that of non-diffusive surface reactions, which have been experimentally shown to yield such species in reasonably high abundances (Fedoseev et al., 2015, 2017; Chuang et al., 2016; Ioppolo et al., 2021).

The presence and distribution of complex, potentially prebiotic molecules within the interstellar medium have been extensively probed using various ground- and space-based observatories. Perhaps the most productive of these studies, however, have been those which have made use of the ALMA for molecular detections (Belloche et al., 2016, 2019; Garrod et al., 2017; Jørgensen et al., 2018; Calcutt et al., 2019; Willis et al., 2020). The impact of ALMA observations on the detection of interstellar molecules has been massive: first detections of prebiotic molecules which were previously controversial or unconfirmed, such as urea (NH₂CONH₂), have been achieved (Belloche et al., 2019), and more information has been gleaned on interstellar chemical processes such as deuteration (Belloche et al., 2016).

To conclude this sub-section, we provide an overview of two especially fruitful ongoing observational projects which include THz/F-IR, millimeter, and centimeter frequencies in their operational ranges: the GOTHAM and ARKHAM projects. These projects are run using the Robert C. Byrd 100 m Green Bank Telescope in the United States and have provided significant data demonstrating the presence of complex organic molecules within interstellar space, with a particular focus on aromatic species. Although operating in a similar fashion, the projects themselves have somewhat different objectives.

The GOTHAM project is primarily concerned with establishing a chemical inventory of the Taurus Molecular Cloud, one of the nearest dense clouds, by performing high-sensitivity wide-band spectral line surveys. Such work is motivated by the fact that benzonitrile (c-C₆H₅CN) was recently discovered in this pre-stellar source (McGuire et al., 2018a), contrasting with a working hypothesis which postulates that larger interstellar aromatic molecules are produced in the circumstellar regions of post-AGB stars and subsequently break down into smaller sub-units such as benzene (c-C₆H₆) under energetic processing (Tielens 2008): so-called “top-down” chemistry. However, these results suggest that reactions between smaller precursor molecules may also contribute to the formation of larger aromatics within pre-stellar regions through a “bottom-up” chemistry approach.

GOTHAM observations of the Taurus Molecular Cloud, combined with laboratory-generated spectra and computational models, have successfully identified many molecules, some of which had not yet been described in the interstellar medium. The unsaturated molecules detected within this dense cloud may play a pivotal role in the formation of larger aromatic molecules, as well as other species relevant to the origins of life. Early work from GOTHAM identified propargyl cyanide (HCCCH₂CN) and the cyanopolyyne HC₁₁N in the Taurus Molecular Cloud (McGuire et al., 2020; Loomis et al., 2021). Cyclic molecules have also been discovered, including 1-cyanocyclopentadiene and 2-cyanocyclopentadiene (Burkhardt et al., 2021a; McCarthy et al., 2021; Lee et al., 2021a). Other cyano and isocyano species have also been detected (Xue et al., 2020; Lee et al., 2021b).

The ARKHAM project is focused on investigating whether the chemistry observed in the Taurus Molecular Cloud is also found in other pre-stellar and proto-stellar sources so as to assess whether or not the resultant molecules survive the birth and evolution of a proto-star. Results from the project have shown that benzonitrile has been detected in four additional sources: Serpens 1A, Serpens 1B, Serpens 2, and MC27/L1521F (Burkhardt et al., 2021b). Such detections illustrate that aromatic chemistry is favorable and extensive throughout the very earliest stages of star formation. Interestingly, the observed abundances of benzonitrile exceeded those predicted by models, despite these models being well-suited to other large carbon-based molecules such as cyanopolyynes. It is therefore probable that the formation mechanisms of other aromatic species in pre-stellar sources differ from those of linear molecules and are not yet well understood.

Joint observational and laboratory investigations are key to deciphering the exact mechanisms of formation of the various complex organic molecules observed within interstellar and circumstellar media. To date, these studies have largely relied on a “bottom-up” chemical perspective in which large complex molecules are produced from simpler starting molecules undergoing some form of processing (such as photolysis or radiolysis). However, as has been demonstrated by the GOTHAM and ARKHAM projects, the formation of certain molecules (such as aromatic species) is likely to be dependent on some combination of “bottom-up” and “top-down” chemistry (McGuire et al., 2020): that is to say that they are formed both from the joining together of smaller molecules, ions, and radicals, as well as the break-up of larger structures (Figure 3).

PAHs are perhaps the best class of interstellar molecules to exemplify the contributions of “top-down” and “bottom-up” astrochemistry due to the fact that they are thought to be relatively ubiquitous in interstellar media, and also because they are able to undergo many chemical transformations yielding a plethora of molecular structures with various sizes, complexities, and arrangements of the aromatic rings, as well as different chemical characteristics such as the inclusion of heteroatoms and the addition of functional groups (such as amino or carboxylic moieties). Indeed, such chemical transformations are thought to be key to the formation of very small grains and fullerenes which result from the respective agglomeration and destruction of PAHs, as well as serving as a carbon feedstock for the production of molecules relevant to biology (Tielens 2008; Groen et al., 2012).

For instance, when mixed with H₂O and subjected to energetic processing (a scenario which is plausible within icy grain mantles in the dense interstellar medium), PAHs have been shown to incorporate oxygen into their molecular structure and display new functional groups such as alcohols, ethers, and ketones (Cook et al., 2015). The addition of a ketone moiety to the PAH is biologically significant, as this provides the base structure for the vitamin K chemical family. Incorporation of heteroatoms (such as oxygen and nitrogen) into the ring structure of the PAH as a result of the energetic processing of mixed icy grain mantles is also possible (Materese et al., 2015), and the resultant heterocyclic molecules are also of great biological significance with nitrogen-containing heterocycles such as pyrimidine and purine being the building blocks for nucleobases.

Pyrimidine has yet to be formally detected within the interstellar medium, however it possesses many similar physico-chemical characteristics to PAHs and so is expected to exist to some extent within icy grain mantles. The UV irradiation of frozen pyrimidine in the presence of H₂O, CH₃OH, NH₃, and CH₄ has been shown to yield the nucleobases uracil, cytosine, and thymine (Nuevo et al., 2009, 2012, 2014; Bera et al., 2016). Similarly, the irradiation of purine in ices containing NH₃ and H₂O leads to the formation of the nucleobases guanine and adenine (Bera et al., 2017; Materese et al., 2017, 2018). Although the idea of an extended lifetime for these nucleobases within interstellar and near-Earth environments has been called into question (Peeters et al., 2003), if there exists some plausible mechanism by which they survive the stellar evolution phases of the astrochemical cycle depicted in Figure 1, then it is possible that they may have been delivered to the early Earth via meteoritic or cometary impacts, thus providing the starting material for the so-called “RNA World Hypothesis”.

The RNA World Hypothesis (Orgel 2004; Bernhardt 2012; Neveu et al., 2013; Higgs and Lehman 2015) hypothesizes that RNA or RNA-like molecules mediated the necessary information processing and metabolic transformations required for life to emerge from the early Earth’s prebiotic environment. Systems based on RNA could act as a precursor to the significantly more complex system of RNA, DNA, and proteins on which current life is based, and it has been recognized that the ribonucleotide co-enzymes now used by many proteins may in fact be molecular fossils from an RNA-based metabolism (White 1976; Raffaelli 2011). The existence of naturally occurring ribozyme catalysts, such as self-splicing introns and the ribonuclease P catalyst (Kruger et al., 1982; Doudna and Cech 2002), along with the fact that ribosomal RNA actually catalyzes the formation of peptide bonds in the ribosome (Lang et al., 2008), has lent some weight to this hypothesis. However, much is still unknown as to the exact mechanisms by which life could arise in the RNA World, and so the hypothesis remains one among many seeking to explain the origins of biology from chemistry.

The “top-down” aspect of PAH astrochemistry has also been considered by previous studies (Merino et al., 2014; Dartois et al., 2020). For instance, Merino et al. (2014) demonstrated experimentally that hydrogen atom interaction with graphene on top of SiC at elevated temperatures triggers an erosion process which results in the ejection of PAH-like flakes. Such results offer an alternative and efficient synthetic pathway for the formation of gas-phase PAHs in the interstellar medium. In the envelopes of evolved stars, SiC condenses to form grains whereupon thermal annealing by the proximal star results in an elemental segregation and the synthesis of a carbon-rich surface (Frenklach et al., 1989; Merino et al., 2014). Exposure of this surface to hydrogen atoms is likely in this environment, and the elevated temperatures (>1000 K) permit a thermally assisted etching effect to take place, thus resulting in the desorption of PAHs.

The dissociation of PAHs themselves into smaller molecules is also a possible process, and has been invoked to explain the interstellar presence of fullerenes, particularly C₆₀. Experimental and modelling studies have shown that PAHs containing 60-66 carbon atoms may be completely dehydrogenated by UV photons to a graphene-like structure, after which the structure folds into a cage. Photon-induced shrinking of the structure then proceeds via the rate-limiting loss of C₂ units until the C₆₀ fullerene structure is attained (Berné and Tielens 2012; Zhen et al., 2014; Berné et al., 2015). The need to further characterize this “top-down” chemistry, particularly as it relates to other smaller carbon-based molecular species which may be relevant to prebiotic chemistry, was highlighted by van Dishoeck (2017).

THz/F-IR laboratory spectroscopy measurements may be acquired using several different methods: Fourier-transform IR spectroscopy (Griffiths and de Haseth 1986), spectroscopy based on photo-mixing (Preu et al., 2011) or parametric conversion (Kawase et al., 1996; Kiessling et al., 2013), backward-wave oscillator spectroscopy (Medvedev et al., 2010), chirped-pulse Fourier-transform spectroscopy (Park and Field 2016), time-domain spectroscopy (Auston, 1975; van Exter et al., 1989; Mittleman et al., 1998), and cascaded frequency multiplication (Drouin et al., 2005; Li and Yao 2010). These methods are all based on the detection of a continuous wave, broadband source, or pulsed THz/F-IR radiation illuminating gaseous or solid (i.e., ice) molecular samples of a species, and having varying frequency spectral ranges, sensitivities, and performances. For example, chirped-pulse spectrometers have a frequency bandwidth of up to 100 GHz (Park and Field 2016), while backward oscillation and time-domain spectrometers have frequency ranges of up to 2.1 THz and 7.5 THz, respectively (Komandin et al., 2013; Allodi et al., 2014).

THz/F-IR time-domain spectroscopy can combine the generation of a THz/F-IR pulse in a zinc telluride crystal via opto-electronic rectification or from plasma filamentation in air using (in both cases) a femtosecond laser with a delay line and opto-electronic detection method in order to record the time domain trace (Allodi et al., 2013). This kind of spectroscopy has been widely used for gas-phase spectral line characterization in vacuum chambers (Kilcullen et al., 2015), in the study of refractive indices (Giuliano et al., 2019), and in the study of intermolecular transitions in astrophysical ice analogues, where the THz/F-IR signal is reflected by or transmitted through the gas or ice. Although it is able to provide critical information regarding the frequency of the spectral transition and the absorption coefficient, it does have a few disadvantages including slow acquisition times and a fine-tuning requirement (Trofimov and Varentsova 2016). As such, these instruments are appropriate only for laboratory settings, and other detectors are usually found in observatories.

One form of THz/F-IR spectroscopy which has found widespread use within laboratory astrochemistry settings is that based on cascaded frequency multiplications (Drouin et al., 2005; Li and Yao 2010). This technology is based on using a sweep synthesizer as the source of radiation, which is used in a phase-locked continuous wave mode during measurements and which has a low phase-noise output. A filter (typically an yttrium iron garnet) is swept simultaneously to this synthesizer so as to suppress any frequency spurs. Frequency sextuplers allow for the production of millimeter radiation having a few milliwatts of power, which is then amplified via the use of microwave integrated circuit amplifiers to generate millimeter radiation with a few hundred milliwatts of power. Cascaded doublers or triplers then follow these amplifiers and generate the submillimeter (i.e., THz/F-IR) wavelength radiation.

Incoherent or direct detector arrays are commonly used in THz/F-IR observatories combined with multiplexer readout systems. They require a higher sensitivity than the photon background noise (such as the microwave background) and high pixel counts. The main technologies used are bolometers (exploiting the neutron transmutation doping process or implanted silicon), superconducting transition-edge-sensed bolometers (TESBs), and kinetic inductance detectors (KIDs) (Farrah et al., 2019). Prior to the development of TESBs and KIDs, bolometers operating at temperatures of 300 K or lower were used in observatories. Incoming radiation results in a change in the detector temperature which is read out as a change in its resistivity. Standard bolometers, however, are limited in their total pixel number which has led to the development and preferential use of other technologies, including TESBs and KIDs.

A TESB consists of a superconducting film operating near its superconducting transition temperature (Henderson et al., 2016; Thornton et al., 2016). The signal is seen as a current through a resistive film at a low temperature of around 100 mK (Suzuki et al., 2016). TESBs have high sensitivities which have allowed them to find use in many space-based instruments, as shown in Table 1. KIDs have a similar sensitivity to TESBs but operate below their superconducting transition temperature; below 300 mK (Griffin et al., 2016). The inductance of the detector material is increased due to broken Cooper pairs from incident photons on the superconducting film. In a resonant circuit, the shift in inductance causes a change in the resonant frequency which may be detected (Day et al., 2003).

Coherent systems used in astronomy are based on the heterodyne detection principle: the THz/F-IR high-frequency (RF) signals from molecules in space are down-converted to a lower frequency band typically of a few GHz known as the intermediate frequency (IF). The IF is easily measurable by sensitive back-ends operating at low frequency (such as power meters, spectrum analyzers, digital spectrometers, etc.). The device used for detection and down-conversion is a mixer which requires the input of a local oscillator (LO) signal at the same frequency as the studied RF signal. LO generators need to have narrow linewidths, low noise, high stability, and a broad tunability with sufficient output power to couple to the mixer. In the THz/F-IR domain, multiple chains based on Schottky diodes and quantum cascade lasers (>3 THz) are most commonly used (Valavanis et al., 2019).

There are three main types of mixers used in radio telescopes: superconductor-insulator-superconductor (SIS) diodes (Kojima et al., 2017), hot electron bolometers (HEBs) (Burke et al., 1999), and Schottky diodes (Maestrini et al., 2010). State of the art SIS diodes and HEBs offer the best system noise temperature performances at around 5–10 times the quantum noise limit. These mixers require only a few microwatts of LO power to operate and are very common for instruments with frequency ranges higher than 1 THz and between 1–6 THz for SIS diodes and HEBs, respectively. SIS diode mixers offer wider IF bandwidths and better sensitivities than do HEBs. However, SIS diodes require cooling to 4 K thus necessitating the use of a complex cryostat. On the other hand, Schottky mixers operate at temperatures above 70 K, a frequency range of up to 3 THz, and an IF bandwidth wider than 8 GHz. Their main disadvantages are their lower sensitivity which is between 30–50 times the quantum noise limit, and their milliwatt LO power requirement (Wilson et al., 2008).

The high-resolution spectroscopy possible when using a coherent detector in telescope facilities is achieved by using a digital technique with real-time fast Fourier-transform (FFT) so as to produce high-resolution spectral data. This idea was first proposed by Weinreb (1961) and has been improved upon over the past 60 years in terms of acquisition speed, frequency bandwidth, power efficiency, cost, and size. Nowadays, three main digital systems are used in astronomy to sample the signal waveform at set time intervals: opto-acoustic spectrometers, digital autocorrelation spectrometers (Emrich 1997), and FFT spectrometers (Klein et al., 2012; Price 2016).

Opto-acoustic spectrometers are based on the diffraction of the signal on a Bragg crystal illuminated by a laser beam and detected by charge-coupled devices. This technique was used in the HIFI instrument aboard the Herschel Space Observatory (Siebertz et al., 2007). The main drawback of this spectrometer is its size, which defines its precision and spectral resolution. Digital autocorrelation spectrometers are based on the multiplication of a signal by a delayed version of the same signal using a series of delays. Spectrum measurement is achieved after the application of a Fourier transformation. Such spectrometers can have a bandwidth of a few GHz with a spectral resolution on the scale of one-hundredth of a kHz. Lastly, FFT spectrometers are based on field-programmable gate array (FPGA) chips. The FPGAs are combined with analogue-to-digital converters having a high data sampling rate of a few GHz samples per second. Their numerous spectral channels decompose the incoming RF signal into small sections giving an instantaneous FFT of a few kHz, as seen on the APEX telescope (Klein et al., 2006).

Since the construction of the first radio telescope in 1937 (Kraus 1988), several telescopes operating in the THz/F-IR range have been successfully built and used by the astronomical community. A principal advantage of performing observations in the THz/F-IR range is the high sensitivity to low-abundance molecules within star-forming regions. Furthermore, observed emission and absorption features can be mapped for all areas within the stellar environment, such as snowlines where ice desorption processes begin to occur.

Progress in the sensitivity of detector technology over the past 50 years has permitted the investigation of interstellar molecular clouds at various wavelengths which has allowed us to improve our understanding of space chemistry. Powerful telescopes have been used with imaging and high spectral resolution instruments combined with large dish antennae. These telescopes have been instrumental in major scientific breakthroughs, such as the discovery of new molecules in the interstellar medium and elucidating the mechanisms for planetary system formation. A summary of the most important telescopes operating in the THz/F-IR range is given in Table 1.

In general, two varieties of observatory exist: ground-based (sometimes also referred to as atmosphere-based) and space-borne telescopes. Ground-based observatories are installed either on the ground at high altitudes or in airborne facilities. Atmospheric transmission has a direct impact on the sensitivity of these observatories at THz/F-IR frequencies since atmospheric molecules (especially H₂O) present strong absorption lines over these frequencies. As such, high atmospheric H₂O content limits atmospheric transmission, thus making observation heavily dependent upon weather conditions and altitude: drier sites to install ground-based telescopes are found at higher altitudes (Figure 5). Brief descriptions of the ground-based ALMA and space-borne Herschel Space Observatory now follow.

ALMA is a ground-based international astronomy facility built over an area of 6596 m² at an altitude of 5000 m located at Llano de Chajnanto in the Atacama Desert, Chile. The 66 high-precision antennae making up the facility are either 12 m (54 of them) or 7 m (12 of them) in diameter. These sizes, combined with the area of the array, give a spatial resolution of 0.2–0.004 arcseconds (1 arcsecond = 1/3,600 degrees). ALMA is composed of ten receivers using Schottky local oscillator sources and SIS diode mixers cooled to 4 K which give up to 16 GHz bandwidth with a spectral resolution of a few kHz. The covered frequency bands range from 31.3–950 GHz in ten windows (Figure 5) with a maximum 8 GHz IF. The lower frequency Bands 1 and 2 are not yet operational. The number of spectral channels available is 4096 per IF. For Bands 3–8, receivers operate in single sideband detection mode acquiring both H and V polarization while Bands 9 and 10 operate in double sideband mode.

Space-based telescopes are not limited by atmospheric attenuations in the way that ground-based observatories are, but do have limitations connected with the size of their antenna aperture. The Herschel Space Observatory was commissioned by the European Space Agency and launched in 2009. The telescope was composed of a 3.5 m diameter dish which was passively cooled by liquid helium at 4 K. Overt time, the liquid helium reserves necessary for detector cooling were gradually depleted, and the end of the telescope’s operations came about in April 2013.

Three scientific instruments were on board the Herschel Space Observatory: a high-spectral resolution heterodyne spectrometer called HIFI (Heterodyne Instrument for the Far-Infrared), an imaging photometer called PACS (Photodetector Camera Array), and a medium resolution grating spectrometer called SPIRE (Spectral and Photometric Imaging Receiver). THz/F-IR frequencies were covered by the HIFI instrument from 408-1908 GHz separated in 12 windows using HEB and SIS diode mixer technology. PACS was composed of a camera integral field spectrometer combined with an imaging photometer operating between 1.427-6 THz and bolometers at frequencies centered around 1.873 THz, 2.997 THz, and 4.282 THz (Rosenthal et al., 2002). Finally, the SPIRE instrument had three main photometers at 600 GHz, 856 GHz, and 119 GHz, as well as a two-band imaging Fourier-transform spectrometer with bolometers operating between 447–1550 GHz (Griffin et al., 2010).

Amongst the key scientific objectives of the Herschel Space Observatory was an investigation of the formation of stellar and planetary systems, and increasing our understanding of the physics and chemistry of the interstellar medium, our Solar System, and extra-galactic galaxies. The HIFI instrument detected more than 100,000 spectral features in a single spectrum (Bergin et al., 2010). Through the Water in Star-Forming Regions with Herschel (WISH) program, many molecules such as H₂O, CO, and O₂ were detected in various astrophysical environments (Goldsmith et al., 2011). Molecules and radicals including H₂O and OH^– were detected further our and deeper in proto-planetary disks than before from surveys of THz/F-IR spectral lines using PACS (Fedele et al., 2013). Cold water reservoirs were discovered in two extra-solar planet-forming disks (TW Hydrae) through the detection of H₂O gas produced by UV photo-desorption of the ice made by HIFI (Hogerheidje et al., 2011). H₂O vapor was also detected in a pre-stellar core at the early stage of stellar formation using HIFI observations combined with models of the UV photo-desorption processes (Casselli et al., 2012).

Ground-based and space-borne observatories operating in the THz/F-IR range, including those listed in Table 1, have aided astronomers in elucidating the chemistry of interstellar space by allowing them to obtain spectroscopic information of molecular species (colloquially termed “molecular fingerprints”). Indeed, the improvement of technology throughout these past decades has allowed for the definitive identification of many new molecular signatures, largely through observation of their rotational emission spectra. Figure 6 shows the comparison of spectra acquired by ALMA Band 10 and the HIFI instrument aboard the Herschel Space Observatory while observing the NGC 6334I region (McGuire et al., 2018b). As can be seen, the number of spectral lines attributed to CO and CH₃OH which are resolved by ALMA Band 10 is significantly higher than that detected by HIFI (Zernickel et al., 2012).

Computer modelling and laboratory measurements of molecular spectra are often needed to assign observed spectral lines to particular molecular species. This is especially true in the case of complex organic molecules such as isopropyl cyanide ((CH₃)₂CHCN), which was the first branched carbon-chain molecule to be detected and which was found in Sgr B2 using the ALMA Band 3 (Belloche et al., 2014). Later, CH₃OCH₂OH and CH₃Cl were observed for the first time by ALMA Bands 6 and 7 in NGC 6334I, and by ALMA Band 7 in IRAS 16293-2422, respectively (Fayolle et al., 2017; McGuire et al., 2017). However, many molecules and radical species may not be observed in the gaseous phase but may play a central role in the formation of observed gaseous species as a result of their presence and reactions in solid icy grain mantles. The use of laboratory THz/F-IR measurements in astrochemical research, particularly as it pertains to solid-phase chemistry, will be elaborated on in the next sub-section.

Over 200 molecules have been detected and spectroscopically resolved in interstellar regions within our galaxy, and more than 60 have been observed in extra-galactic molecular clouds (Müller et al., 2005), ranging in complexity from simple diatomics to the more structurally complex fullerenes and PAHs. An overarching aim of laboratory astrochemistry is to be able to understand the physico-chemical processes which occur in these astrophysical environments so as to better comprehend the chemical reactions which lead to the formation of such molecules. Such work is motivated by the knowledge that such reactions can result in the production of various molecules and minerals. For instance, interstellar biomolecules which may form in dense, quiescent molecular clouds may be subsequently incorporated into the stellar and planetary systems which evolve from these clouds and thus play a defining role in the emergence of life within these systems (Watanabe and Kouchi, 2002; Jones et al., 2011; Fedoseev et al., 2017; Chuang et al., 2020; Sandford et al., 2020; Ioppolo et al., 2021). The synthesis of smaller, volatile molecules in astrophysical environments is equally important, as such molecules may contribute to the development of planetary and lunar atmospheres or transient exospheres (Milillo et al., 2016; Teolis and Waite 2016). Additionally, condensation processes and grain alterations contribute to the formation of minerals which are significant to the geological and geochemical evolution of planets and moons, including graphite, corundum, moissanite, and forsterite (Frenklach et al., 1989; Hazen et al., 2008; Hazen and Ferry 2010).

The unambiguous identification of such molecules by infrared and radio telescopes (including those which operate in the THz/F-IR range) relies on the availability and completeness of gas- and solid-phase spectroscopic databases at the corresponding frequencies for a great variety of molecules. Such information is obtained by performing classical laboratory measurements (Wlodarczak 1995; Smith 2011; Cataldo et al., 2013a; Allodi et al., 2013; Widicus-Weaver 2019; Mifsud et al., 2021). Presently, the two most commonly referenced catalogues are the Cologne Database for Molecular Spectroscopy (Müller et al., 2001; Endres et al., 2016) and the Jet Propulsion Laboratory (Pickett et al., 1998) catalogues, which give the frequency and amplitude of several molecular transitions. Two accessible databases listing vibrational transitions at IR wavelengths are also available: the HITRAN database (Rothman et al., 2009) and the EXOMOL line list.

Broadly speaking, laboratory astrochemistry studies are largely concerned with investigating reactions which occur in either the gas phase or the condensed (ice) phase. Experiments are typically performed using high or ultra-high vacuum chambers. For instance, a novel method of performing gas-phase spectroscopy is to make use of a heterodyne radiometer so as to observe the absorption features of various gaseous species within the chamber, thus functioning in a similar fashion to several telescope facilities. Two laboratory broadband emission THz/F-IR radiometers based on heterodyne detection methods have been developed: the first is based on Schottky-barrier technology combined with a FFT digital spectrometer operating between 80 and 110 GHz (Wehres et al., 2017), while the second is based on cryo-cooled SIS diode mixer technology operating between 270 and 290 GHz (Wehres et al., 2018). By using such instruments, the spectroscopic features of pyridine and CH₃CN have been successfully measured and matched with analytical simulations. Similarly, a Schottky-based receiver has been used in combination with a FFT digital spectrometer and vacuum chamber to observe the emission line of N₂O at 355.6 GHz (Parkes et al., 2018).

Laboratory experiments concerned with the solid phase also require the use of high or ultra-high vacuum chambers, wherein interstellar ice analogues may be synthesized on cold substrates via the direct or background deposition of dosed gases or vapors, or the effusive evaporation of refractories. The deposited ices are then processed in such a way as to simulate astrophysical conditions: atom (or free radical) additions represent non-energetic pathways towards molecule formation (Linnartz et al., 2015; Chuang et al., 2016; Potapov et al., 2017; Ioppolo et al., 2021); bombardment with energetic charged particles (i.e., electrons and ions) simulates ice interactions with galactic cosmic rays, the solar wind, or planetary magnetospheric plasmas (Baragiola et al., 1999; Dalton et al., 2013; Ding et al., 2013; Boamah et al., 2014; Boduch et al., 2015; Fulvio et al., 2018; Ioppolo et al., 2020; Garozzo et al., 2010); irradiation with photons (both ionizing and non-ionizing) simulates extra-terrestrial photochemistry (Bernstein et al., 2002; Lo et al., 2014; Öberg 2016; Mullikin et al., 2018); energetic shocks simulate collisions between interstellar or Solar System bodies (Goldman et al., 2010; Martins et al., 2013), and thermal processing simulates the chemical and structural changes induced within interstellar icy grain mantles proximal to nascent stars, or in Solar System bodies as they approach perihelion (Ehrenfreund et al., 1999; Kaňuchová et al., 2017).

The changes in the physico-chemical properties of the ice analogues induced by such processing have been traditionally monitored using mid-IR or UV-VIS spectroscopy (Mason et al., 2006; Boersma et al., 2014). This has been advantageous in that such laboratory work is complementary to observational work using space-borne telescopes working within these ranges of the electromagnetic spectrum, such as the Spitzer Space Telescope and the Hubble Space Telescope. Although not yet widely used within laboratory settings, the utility and applicability of THz/F-IR spectroscopy is being increasingly recognized due to its ability to detect lower frequency molecular vibrations, as well as intermolecular interactions and translational vibrations within solid lattices (Bertie 1968; Bertie and Jacobs 1977; Kulesa 2011; McIntosh et al., 2012). The remainder of this sub-section will be devoted to a discussion on the application of THz/F-IR spectroscopy to laboratory studies of astrophysical ice analogues.

THz/F-IR spectra differ depending upon the structural morphology of the ice (e.g., amorphous or crystalline solid phases), as demonstrated by Moore and Hudson (1992, 1994, 1995). For instance, recent studies investigating CO₂ in H₂O and CH₃OH ice matrices at various temperatures have revealed that the measured THz/F-IR spectra are especially sensitive to the degree of segregation within the ice structure. Results have shown that CO₂ roaming during warming of the ice results in a localized accumulation, or segregation. When mixed with crystalline H₂O ice, this CO₂ segregation results in a disruption of the hydrogen bonding network between adjacent H₂O molecule layers, causing the H₂O spectral resonance features to be shifted, distorted, or attenuated (Allodi et al., 2014). On the other hand, CO₂ absorption bands were observed to become narrower and more defined when segregation from CH₃OH ice occurred as a result of warming (McGuire et al., 2016).

Such work clearly demonstrates the sensitivity of THz/F-IR spectroscopy not only to the nature of the chemical species present within the ice, but also to the physical structure of the ice. Given that the nature of the observed spectral absorption features is dependent upon the temperature, degree of crystallinity, segregation, and thermal history of the ice, THz/F-IR spectroscopy appears to be highly suitable for assessing not only the composition and temperature characteristics of astrophysical ices, but also their morphology (Ioppolo et al., 2014). To date, relatively few of the observed molecules have been investigated using THz/F-IR spectroscopy. Amorphous solid H₂O, for instance, presents a spectral line at 1 THz. CH₃OH, CH₃CHO, and (CH₃)₂CO have been found to have a broad feature at around 4 THz, while in HCOOH and CH₃COOH this broad absorption feature is centered at about 7 THz (Ioppolo et al., 2014).

Laboratory THz/F-IR spectroscopy has also been used in the analysis of more complex molecular structures such as PAHs. Although these molecules are believed to be ubiquitous in interstellar and circumstellar media (Tielens 2008; Kwok and Zhang 2011), few single structures have been positively identified (McGuire et al. 2021). Systematic analysis of a series of PAHs, as well as their hydrogenated and alkylated derivatives, has revealed that the THz/F-IR spectra of these molecules display so-called “Jumping Jack” modes which correspond to the in-plane vibrations around the central molecular core (Cataldo et al., 2013b). As such, these spectra provide crucial information related to the number of fused aromatic rings present within the molecule, and are thus valuable in identifying the individual molecular carriers of PAH diffuse interstellar absorption bands. Other complex molecules, including those which may be of relevance to prebiotic chemistry, have also been studied using THz/F-IR spectroscopy (Widicus-Weaver et al., 2005; Carroll et al., 2010).

Recently, a new laboratory-based method for observing desorption mechanisms occurring within the interstellar medium and star-forming regions has been developed. Studying such desorption has been traditionally performed using mid-IR spectrophotometers and quadrupole mass spectrometers, however this has the drawback of not being able to detect ions and radicals and is difficult to relate to observations made using radio telescopes (Fraser et al., 2002; Collings et al., 2003; Fuchs et al., 2009; Muñoz-Caro et al., 2010). In principle, it is possible to desorb (either via thermal or non-thermal mechanisms) ices formed of pure or layered molecules and observe the resultant gas phase in the THz/F-IR frequency range. One way to do this is to passively observe the emission of those molecules during desorption in an astrochemical chamber equipped with a heterodyne radiometer (Auriacombe et al., 2015, 2016); another is by performing microwave absorption spectroscopy. The region in which desorbing molecules are observed may be directly above the ice, and the relevant spectral transitions may be detected with a HEB (see Figure 2 in Yocum et al., 2019). Alternatively, a chirped-pulse Fourier-transform spectrometer can be used to observe the desorption occurring inside a waveguide (Theulé et al., 2020). These emerging techniques are capable of bringing new insights and possibilities to our understanding of the desorption processes in star-forming regions.

Although the use of THz/F-IR spectroscopy is growing within laboratory-based astrochemical research (driven by developments in the relevant technologies and an increase in the commercial availability of the necessary spectrometers), much of the current work takes place at large-scale facilities. A complete and thorough description of the research conducted using THz/F-IR radiation at such facilities would go beyond the scope of this review, and we instead direct the interested reader to other works (e.g., Neil 2014). However, it is worthwhile to take some time to briefly describe the Free Electron Lasers for Infrared Experiments (FELIX) facility located in Nijmegen, the Netherlands, where an ultrahigh-vacuum chamber has been installed as the Laboratory Ice Surface Astrophysics (LISA) end-station thus permitting the characterization of astrophysical ice analogues which have been processed as a result of THz/F-IR irradiation.

The FELIX facility is home to four free electron lasers which provide short-pulsed coherent light covering the microwave to mid-IR regions of the electromagnetic spectrum. The FELIX-1 and FELIX-2 free electron laser beamlines respectively operate over the ∼65–330 cm⁻¹ and ∼225–3300 cm⁻¹ ranges and are capable of providing bursts of micro-pulses with selective and tunable wavelengths whose duration may be readily controlled. These beamlines are therefore highly suited to providing THz/F-IR (as well as mid-IR) radiation for use in laboratory studies of astrophysical ice analogues, which are prepared in the LISA end-station.

The LISA is an ultrahigh-vacuum chamber with nominal base pressure in the region of a few 10⁻¹⁰ mbar containing an elongated rectangular gold-coated deposition substrate which may be cooled down to 15 K using a closed-cycle helium cryostat head with a cooled compressor. The gold-coated substrate is manipulated by means of a xyz-linear translator allowing for the irradiation of different spots of the ice during a single experiment, as well as a rotary stage mostly employed for alignment purposes. Pure gases and gas mixtures are pre-prepared in a dosing line prior to being injected into the main chamber via an all-metal leak valve, wherein background deposition of the gases occurs to form the astrophysical ice analogues. Such background deposition of gases onto the deposition substrate allows for a more uniform ice deposition, and the resultant ice analogue may be used in systematic studies. Ices processed by mid-IR or THz/F-IR irradiation delivered by the FELIX beamlines may be monitored in two ways: mid-IR reflection-absorption spectroscopy may be used to monitor any physico-chemical effects induced as a result of the ice stimulation, and quadrupole mass spectrometry may be used to monitor species which desorb thermally from the bulk parent ice.

The FELIX-LISA facility has found regular use in effectively characterizing the physico-chemical changes induced in astrophysical ice analogues as a result of stimulation by incident irradiation. For instance, Noble et al. (2020) investigated the effect of resonant irradiation of amorphous solid H₂O using mid-IR radiation supplied by the FELIX-2 beamline. Their results indicated that irradiation with wavelengths corresponding to the mid-IR stretching, bending, and libration modes of amorphous H₂O resulted in a wide-ranging structural rearrangement of the ice into a crystalline-like form due to vibrational relaxation of the intermolecular hydrogen bonding network. Results such as these, combined with the experimental capabilities of large-scale facilities such as FELIX, make future dedicated studies looking into the irradiation of lower frequency THz/F-IR modes of astrophysical ice analogues especially attractive.

As has been demonstrated, the application of THz/F-IR spectroscopy to observational and laboratory astrochemistry has the potential to unravel much information related to the structure and reactivity of molecules in space. To date, however, THz/F-IR experiments at large-scale facilities such as FELIX tasked with investigating the chemistry of interstellar and Solar System ice analogues have not been explored to their fullest potential due to the fact that the dedicated pump-probe experiments required to study such chemistry are not available at the time of writing. The present LISA end-station configuration comprises an FTIR spectrophotometer with an extended spectral range to the far-IR. Such a system may be used to time-resolve transient events within the ice structure (such as diffusion of molecules through different ice layers and segregation events in mixed ices) at millisecond timescales.

To fully benefit from the unique capabilities of a free electron laser (i.e., a wide-range tunability, high peak power, and a controllable repetition rate), THz/F-IR time-domain spectroscopy with single-shot detection techniques should be employed to extend time resolutions to a few tens of picoseconds (Redlich et al., 2003; Perakis et al., 2013; Shalit et al., 2013; Mead et al., 2019). With such a configuration, free electron laser THz/F-IR radiation could be used to “pump” (i.e., inject energy into) inter- and intramolecular vibrations of solid species that, having been excited by the sudden excess of energy, will subsequently rearrange selectively or diffuse within the ice and possibly react with other species. Diffusion and reaction of molecules could be triggered and controlled by operating a free electron laser across its spectral range and could then be monitored by means of a THz/F-IR single-shot spectrometer in the solid phase, while desorbed species could be monitored by implementing a broadband emission THz/F-IR radiometer as described previously. The combination of a free electron laser and new advanced techniques in laboratory astrochemistry thus has the potential to reveal unprecedented details on fundamental phenomena which could play important roles in the formation of complex prebiotic molecules in space, and would thus expand our understanding of the relevant extra-terrestrial physics and chemistry.

Experimental work such as that proposed to be performed at the FELIX-LISA facility on broadband emission THz/F-IR radiometry would also contribute much to our interpretation of observational data. The importance of commissioning new space-borne observational facilities operating in the THz/F-IR was highlighted in the recently published Pathways to Discovery in Astronomy and Astrophysics for the 2020s roadmap (National Academies of Sciences, Engineering, and Medicine, 2021), particularly in light of the fact that the Space Infrared Telescope for Cosmology and Astrophysics (SPICA) is no longer being considered for launch. Interestingly, the far-IR is one of the spectral ranges where astronomical data with sub-arcsecond resolution is not currently available: a fact which is somewhat at odds with the potential usefulness of spectroscopic measurements in this range (Linz et al., 2021). A number of space-based observatories, such as the Far-Infrared Spectroscopic Surveyor (FIRSS) and the Terahertz Exploration and Zooming-In for Astrophysics (THEZA) telescopes have also been proposed to fill in this gap (Gurvits et al., 2021; Rigopoulou et al., 2021), and the acquisition of laboratory reference data will doubtlessly aid in further characterizing the molecular composition of the cosmos.