Abstract
Molecular hydrogen has two nuclear-spin modifications called ortho and para. Because of the symmetry restriction with respect to permutation of the two protons, the ortho and para isomers take only odd and even values of the rotational quantum number, respectively. The ortho-to-para conversion is promoted in condensed systems, to which the excess rotational energy and spin angular momentum are transferred. We review recent studies on fast ortho-to-para conversion of hydrogen in molecular chemisorption and matrix isolation systems, discussing the conversion mechanism as well as rotational-relaxation pathways.
1 Introduction
Molecular hydrogen has a remarkable feature of nuclear-spin isomers. According to the quantum number I of the total nuclear spin, a hydrogen molecule has two modifications called ortho (I = 1) and para (I = 0) species. Because of the symmetry restriction, ortho (para) H2 takes only odd (even) values of the rotational quantum number J. Whereas the transition between ortho and para species is strictly forbidden in the isolated state, it is significantly promoted upon interaction with other substances. Because the nuclear-spin isomers are identified by I and J, the ortho-to-para (o-p) conversion of H2 involves two aspects of the nuclear-spin flip and the rotational-energy transfer to a surface or a surrounding material.
The gas-surface energy transfer has been one of the main topics in surface physics and chemistry; a typical example is the adsorption event, where the translational and adsorption energy of a molecule is transferred to a surface. In addition to the translational energy, internal degrees of freedom such as molecular vibration and rotation are also of considerable importance. Owing to the advance in laser techniques, the relaxation processes of vibrationally-excited molecules have been well studied to date (; ; ; ; ; ). Compared to the vibration, on the other hand, the energy transfer from the molecular rotation to surface degrees of freedom has been poorly understood. One promising approach for the elucidation of the rotational-energy transfer is to investigate the o-p conversion of H2 on surfaces and in matrices. After adsorption on a cold surface or trapping in a matrix, ortho (para) H2 predominantly occupies its lowest rotational level with J = 1 (J = 0). Upon o-p conversion of H2, the rotational-energy needs to be dissipated into surface or matrix degrees of freedom.
The o-p conversion of H2 has been observed on various systems (). The o-p conversion is closely related to the quest for efficient ways of the H2 storage (), and therefore is being investigated not only on surfaces but also inside solids (; ; ) and nano-cages (; ; ). Stimulated by the development of the experimental investigations, several conversion mechanisms have been also proposed depending on the interacting materials (): the Wigner model (), where the proton spin interacts with the inhomogeneous magnetic field generated by localized paramagnetic ions; the electron-spin-induced conversion models categorized into the second- () and third-order () perturbation theories, where the virtual electron exchange or transfer between H2 and a surface is involved along with the Fermi contact interaction between an electron and a proton in H2; the electric-field-induced conversion model (), where the Stark, spin-orbit, and Fermi-contact couplings mix the ortho and para states.
In spite of the extensive studies on the H2o-p conversion in the last decades, there still remain controversial issues; one is fast conversion and the other is the rotational-energy dissipation. In contrast to the o-p conversion time of ~ 103 s or longer observed on various surfaces and in solids, H2o-p conversion with a time constant shorter than ~ 102 s was recently observed on Pd(210) and inside a molecular solid of CO2. On the Pd(210) surface, furthermore, rotational-energy transfer was investigated in detail taking account of electrons and phonons of surfaces. In this review paper, we expound the studies of the fast o-p conversion in a CO2 matrix (Section 2) and on Pd(210) (Section 3), discussing the spin and rotational-energy transfer.
2 Matrix isolation system
The techniques of nuclear magnetic resonance (NMR), neutron scattering, Raman spectroscopy, and infrared absorption spectroscopy have been applied to in situ observation of the H2 conversion in fullerene (C60) (; ; ), metal-organic frameworks (MOFs) (), porous coordination polymers (), semiconductors (; ; ), and viscous organic solutions (), as was reviewed recently (). Whereas NMR directly probes the nuclear spin, the other methods enable one to resolve the rotational states of ortho- and para-H2. In the nuclear-spin conversion study of polyatomic molecules such as H2O (; ; ), NH3 (; ; ), and CH4 (; ; ), the most popular technique has been rovibrational spectroscopy combined with the matrix-isolation method, where target molecules are isolated in molecular solids, e.g., rare-gas ones. Indeed, the temperature dependence of the conversion rate has been intensively studied in this way to reveal the pathways for the rotational relaxation (; ; ).
Since H2 is the lightest molecule and has a relatively small interaction with matrix molecules, rather low temperatures (typically T < 15 K) are required to suppress its diffusion and formation of aggregates. In previous studies, the ortho and para isomers of H2 have been separately detected in various matrices of Ar, Kr, Xe, N2, and CO by using Raman spectroscopy (; ; ). In particular, Alikhani et al. kept Ar-isolated H2 at 9 K for 24 h and observed no change of the intensity ratio of the ortho and para signals, which means the o-p conversion was suppressed significantly in solid Ar. In contrast, comparing the ratio with a calculated value, the o-p conversion was found to partially proceed just during the sample deposition; they pointed out the possibility that this conversion was catalyzed by O2 impurities. Although H2 has no permanent electric dipole moment, one is able to detect matrix-isolated H2 also by infrared absorption spectroscopy because of its weak polarization. Warren et al. measured infrared spectra of H2 trapped inside Ar, Kr, N2, and CO matrices in the wavenumber regions of pure rotational and vibrational transitions; except for the rotational spectrum of Kr-isolated H2, the ortho and para signals were resolved (). They also found the ortho-to-para ratio of H2 trapped in solid Ar to be decreased by ∼25% after 2–3 days and attributed this o-p conversion to the accidental contamination of magnetic impurities, though the accurate conversion rate was not determined. In a recent study (), H2 was trapped and polarized in solid CO2, so that the conversion rate of H2 was derived from the time evolution of its infrared absorption band, as is expounded below.
The room-temperature gaseous mixture of CO2 and H2 at a molar ratio of CO2/H2 = 100 was condensed onto a gold substrate at 5.4 K for 10 min, and infrared spectra were measured in the reflection configuration. From the film interference pattern appearing in the baseline of the spectrum, the thickness of the CO2 matrix was determined to be 4.5 . Just after the condensation, the spectrum showed not only intense absorption bands of CO2 but also a weak band of H2. At a trapping site of H2, the electric fields generated by surrounding CO2 molecules did not cancel each other out, resulting in slight electric-polarization of H2. The time evolution of the H2 band after the sample deposition is displayed in Figure 1A. The absorption band was well-reproduced by the combination of three gaussian curves: G1 at 4,149 cm−1, G2 at 4,147 cm−1, and G3 at 4,138 cm−1. Whereas G1 grew with increasing time, G3 decayed and finally disappeared. This time development was attributed to the conversion of H2 from ortho to para; in other words, G1 and G3 were assigned to the Q1 (0) and Q1 (1) transitions of para- and ortho-H2, respectively. In the gas phase, the transition energy of Q1 (0), 4,161.1 cm-1, is also higher than that of Q1 (1), 4,155.3 cm−1 (), owing to the rovibrational coupling in H2. As shown in Figure 1B, the integrated intensities of Gm (m = 1, 3) were analyzed as a function of time, and were found to follow the monoexponential function:where and denotes the initial and equilibrium intensities, respectively. The conversion rate derived from G1, , coincided within error with that from G3, .
FIGURE 1
To reveal the origin of G2, Yamakawa et al. also investigated the time evolution of the infrared spectrum just after the sample deposition, as shown in Figure 1C; in the time range of , an additional component, G4, was detected at 4,141 cm−1, and the decay of G4 was observed simultaneously with the growth of G2. Thus, it was likely that there were two kinds of trapping sites for H2 inside solid CO2; while G1 and G3 were attributed to H2 at site A, G2 (G4) was to para (ortho) H2 at site B. The frequency difference between the para and ortho species at site B was about a half of that at site A. This suggests the approach of the lowest rotational levels of ortho- and para-H2 and relatively high anisotropy of the confining potential at site B. Note that the estimated o-p conversion rate at site B was as high as . In a previous study with use of electron-energy-loss spectroscopy, the conversion rate of H2 adsorbed on the stepped surface of Cu(510), where the adsorption potential is strongly anisotropic, was evaluated to be on the order of 1 s (). These results suggest fast conversion of rotationally hindered H2, which is also shown in Section 3.
In most of the condensed systems, the vibrational-frequency shift of H2 with respect to the gas phase, , was negative: () cm-1 at site A (B) of solid CO2 (), cm-1 in solid N2 and CO (), cm-1 on amorphous D2O ice (). Despite the relatively small red-shift, the conversion rate of H2 in solid CO2 at 5.4 K was even higher than that on amorphous H2O ice at 9.2 K, , measured by , who also reported the monotonical increase of the rate with temperature below 14 K. This result is not explained by the electric-field-induced conversion mechanism (); instead, probable is the three-step conversion model (; ), which consists of electron exchange between H2 and a solvent, hyperfine contact interaction in H2, and spin-orbit interaction inside the solvent.
Interestingly enough, the conversion time-constants (the inverse of the conversion rate) of H2 in non-magnetic systems accompanied by energy gaps are distributed quite widely: a few or tens of minutes in MOFs () and solid CO2 (), and tens or hundreds of hours in crystalline Si (; ; ) and the cage of C60 (). Note that the CO2 film deposited below ∼9 K has a porous structure with the enhanced surface area and exhibits a unique feature of “thermal spikes”, which are abrupt temperature rises due to the structural rearrangement during the film deposition (). The enhanced o-p conversion of H2 is possibly related to the characteristically unstable and porous structure of the CO2 film. In order to further investigate the origin of the large difference in the conversion time, the electronic structure of the H2-solvent system, including the anisotropy of a confining potential, should be also studied. The temperature dependence of the conversion rate of H2 trapped in matrices is under investigation and will bring about information on the channels of the rotational relaxation, just like the surface system described in the following section.
3 Molecular chemisorption system
As typical adsorption schemes of H2, dissociative chemisorption and molecular physisorption are recognized. In most of past studies on o-p conversion at surfaces, H2 in the physisorption state via the van der Waals interaction was focused, in which the molecule is in a nearly-free rotational state (; ). On the other hand, some stepped surfaces exhibit a peculiar adsorption of molecular chemisorption (; ; ; ; ; ; ), in which the adsorption potential is anisotropic with respect to the molecular-axis angle and the rotational motion is strongly hindered. Although the rotational state is modified under the anisotropic potential, the rotational state of H2 chemisorbed on surfaces is correlated with the nuclear-spin state, either ortho or para. In the past, while the occurrence of fast o-p conversion under an anisotropic potential was indicated for the systems of Cu(510) and Pd(210), direct evidence was lacking due to the limited time resolution of the experimental technique used in previous studies (; ). In this section, fast o-p conversion and associated rotational-energy transfer are discussed for H2 molecularly chemisorbed on Pd(210).
The Pd(210) surface has (100) terraces with steps running along the [001] direction forming open (110)-like microfacets. H2 chemisorbs on the step-edge of Pd atoms, so that H2 binds strongly to the surface compared with the physisorption systems (). The adsorption state of H2 has been studied experimentally and theoretically (; ; ). The H2 adsorption potential is highly anisotropic, which induces lifting of the rotational state degeneracy of the triply degenerate J = 1 state in gas-phase into doubly degenerate state (m = ±1, m: z component of J) and a non-degenerate state (m = 0) in the adsorption state. Hence the lowest o-H2 (m = ±1) behaves like a two-dimensional rotor ().
To track the fast o-p conversion directly, a new experimental method was developed by combining a pulsed molecular beam (MB), photo-stimulated desorption (PSD), and resonance-enhanced multiphoton ionization (REMPI). Figure 2A shows a schematic diagram of the experimental setup and a timing chart of the MB-PSD–REMPI measurement for probing the time evolution of the rotational states of H2 on surfaces (). Probing the change in the rotational state distribution allows us to track o-p conversion owing to the fact that the rotational states of H2 couple with nuclear spins. With n-H2 molecular beam deposition, the o-p ratio at a surface temporarily becomes out-of-thermal-equilibrium, and then relaxes to the thermal equilibrium. From the change in the two nuclear-spin-state populations as a function of the adsorption time, the conversion rate can be determined, similar to that shown in Figure 1B. The conversion rate has been successfully determined on Pd(210) as a function of the surface temperature (TS) in the range of 41–60 K as shown in Figure 2B. It is found the conversion rate increases with increasing temperature. Note that the values of the conversion time (inverse of conversion rate) are on the order of 1–10 s, demonstrating the occurrence of fast conversion on Pd(210).
FIGURE 2
Since the o-p conversion is accompanied by the rotational transition as well as the nuclear spin flip, the surface temperature dependence of o-p conversion allows us to investigate the rotational-energy (Erot) transfer process in o-p conversion. The rotational-energy dissipation process has been discussed in previous studies on the o-p conversion of physisorbed H2 on amorphous solid water, silicate and carbon materials (; ; ). These studies suggested that substrate phonons play an important role in the rotational-energy transfer in the conversion. Depending on the substrate, two kinds of phonon dissipation process have been considered in those studies; one-phonon and two-phonon processes. Whereas in the former process the rotational energy is dissipated into the surface by excitation of a phonon, the latter process proceeds via the simultaneous absorption of a phonon from the initial up to an intermediate state, and the emission of another from the intermediate to the final states (). Since those materials are all non-metallic, the influence of surface electrons in the rotational-energy transfer process can be neglected.
On the other hand, Pd is a non-magnetic metal, where substrate electrons are expected to play an important role in analogy with the vibrational-energy relaxation. A widely accepted conversion model on a non-magnetic metal surface is the electron-exchange-hyperfine-contact (XY) model proposed by Ilisca () (Figure 2C-(a)). In this model, an electron in the σg orbital of H2 is excited to the surface and an electron in the surface is excited to the σu orbital of H2 with the Coulomb interaction, followed by nuclear-spin flip with the Fermi contact hyperfine interaction between the electron in the σu orbital and the hydrogen nuclei leading to the o-p conversion. Consequently, a surface electron is excited to the level above the Fermi level (EF) by the amount of Erot, and thus Erot is dissipated into metal electron-hole pairs. Assuming that the electron transfer probability is independent of its energy, the o-p transition probability in this model is proportional to the numbers of electron and hole states available. The calculated transition probabilities are plotted in Figure 2B, showing that the transition probability does not change significantly with TS, which is inconsistent with the experimental data. Therefore, two combination models based on the XY model, namely, Erot transfer is shared by both electronic transition and phonon excitation through either one-phonon or two-phonon processes, are proposed (Figure 2C-(b)(c)). It should be mentioned that the electron transition process is essential for nuclear-spin flip via the Fermi contact hyperfine interaction. The results of both combination models in Figure 2B show that the transition probability varies substantially with TS in contrast with the result based on the XY model. Particularly, the tendency of the combination model of electronic transition and two-phonon process is in good agreement with that of the experimentally determined o-p conversion rate. This indicates that the rotational energy of H2 transfers into not only electrons but also phonons of surfaces ().
Recalling the fact that the vibrational energy is transferred to electrons at metal surfaces, this rotational-energy transfer process might be counterintuitive, because Erot is transferred into phonons as well as electrons of surfaces despite a metallic surface. The difference between vibrational- and rotational-energy transfer paths could be ascribed to the energy scale of both degrees of freedom. While the magnitude of the rotational energy of H2 ( ~ 10 meV) is much smaller than the vibrational energy such as the CO stretch mode (∼0.26 eV), that is comparable with the magnitude of the substrate phonon energy. The energy transfer path might be determined by the energy-scale matching between the molecular degree of freedom and surfaces as a receiver.
4 Concluding remarks
We have expounded a recent advance in the o-p conversion study of H2, dealing with the fast conversion in the two novel systems characterized by the matrix isolation and molecular chemisorption. It is notable that the conversion time-scale was ~ 102 s or shorter in spite of the non-magnetic properties of these systems. While a variety of metal oxides have been investigated as the magnetic catalysts of the H2o-p conversion for many decades, expanding needs for the efficient H2 storage and high-performance electrodes for the water electrolysis promotes the studies of H2 interacting with non-magnetic substances such as MOFs and carbon nanomaterials. Since the o-p conversion involving both the spin- and energy-transfers influences the storage and chemical reaction of H2, further studies of the conversion mechanism in the non-magnetic systems are required to reveal the determinant of the conversion time-scale. The anisotropy of a confining potential should be one of the key factors, and the temperature dependence of the conversion rate will provide essential information on the rotational-relaxation pathways also in other systems.
Statements
Author contributions
HU: Writing–original draft, Writing–review and editing. KF: Writing–review and editing. KY: Writing–original draft, Writing–review and editing.
Funding
The authors declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Japan Society for the Promotion of Science (KAKENHI; Grant JP18H05518, JP20K05424, JP20K05337, JP21H04650, JP23H01856, and JP23K04593) and Grant for Basic Science Research Projects from the Sumitomo Foundation. HU was partially supported by MEXT Japan, Leading Initiative for Excellent Young Researchers.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
1
Abouaf-MarguinL.VasserotA. M.PardanaudC.MichautX. (2007). Nuclear spin conversion of water diluted in solid argon at 4.2K: Environment and atmospheric impurities effects. Chem. Phys. Lett.447 (4–6), 232–235. 10.1016/j.cplett.2007.09.014
2
AlikhaniM. E.SilviB.PerchardJ. P.ChandrasekharanV. (1989). Reinvestigation of the Raman spectra of dihydrogen trapped in rare gas solids. I. H2, HD, and D2 monomeric species. J. Chem. Phys.90 (10), 5221–5231. 10.1063/1.456475
3
ArakawaI.KobayashiM.TuziY. (1979). Effects of thermal spikes on the characteristics of cryosorption pumps with condensed carbon dioxide layers. J. Vac. Sci. Technol.16 (2), 738–740. 10.1116/1.570072
4
ArguellesE. F.KasaiH. (2018a). Bound nuclear spin states of H2 in an anisotropic potential induced by a stepped metal surface. J. Vac. Sci. Technol. A Vac. Surfaces, Films36 (3), 030601. 10.1116/1.5023158
5
ArguellesE. F.KasaiH. (2018b). Hindered rotation and nuclear spin isomers separation of molecularly chemisorbed H2 on Pd(210). J. Appl. Phys.123 (11), 115301. 10.1063/1.5021994
6
AroulandaC.StarovoytovaL.CanetD. (2007). Longitudinal nuclear spin relaxation of ortho- and para-hydrogen dissolved in organic solvents. J. Phys. Chem. A111 (42), 10615–10624. 10.1021/jp073162r
7
BeckerleJ. D.CasassaM. P.CavanaghR. R.HeilweilE. J.StephensonJ. C. (1990). Ultrafast infrared response of adsorbates on metal surfaces: Vibrational lifetime of CO/Pt(111). Phys. Rev. Lett.64 (17), 2090–2093. 10.1103/PhysRevLett.64.2090
8
BoisselP.Gauthier‐RoyB.Abouaf‐MarguinL. (1993). Dipolar interactions between NH3 molecules trapped in solid argon. II. Line narrowing during nuclear spin species conversion. J. Chem. Phys.98 (9), 6835–6842. 10.1063/1.464775
9
CarravettaM.DanquignyA.MamoneS.CudaF.JohannessenO. G.HeinmaaI.et al (2007). Solid-state NMR of endohedral hydrogen–fullerene complexes. Phys. Chem. Chem. Phys.9 (35), 4879–4894. 10.1039/B707075F
10
CarravettaM.JohannessenO. G.LevittM. H.HeinmaaI.SternR.SamosonA.et al (2006). Cryogenic NMR spectroscopy of endohedral hydrogen-fullerene complexes. J. Chem. Phys.124 (10), 104507. 10.1063/1.2174012
11
CarravettaM.MurataY.MurataM.HeinmaaI.SternR.TontchevaA.et al (2004). Solid-state NMR spectroscopy of molecular hydrogen trapped inside an open-cage fullerene. J. Am. Chem. Soc.126 (13), 4092–4093. 10.1021/ja031536y
12
ChangH.-C.EwingG. E. (1990). Infrared fluorescence from a monolayer of CO on NaCl(100). Phys. Rev. Lett.65 (17), 2125–2128. 10.1103/PhysRevLett.65.2125
13
ChenJ. Y.-C.LiY.FrunziM.LeiX.MurataY.LawlerR. G.et al (2013). ‘Nuclear spin isomers of guest molecules in H2@C60, H2O@C60 and other endofullerenes’, Philosophical Trans. R. Soc. A Math. Phys. Eng. Sci., 371, p. 20110628. 10.1098/rsta.2011.0628
14
ChenL.LauJ. A.SchwarzerD.MeyerJ.VermaV. B.WodtkeA. M. (2019). The Sommerfeld ground-wave limit for a molecule adsorbed at a surface. Science363 (6423), 158–161. 10.1126/science.aav4278
15
ChristmannK. (2009). Interaction of hydrogen with (210)-oriented metal surfaces: Molecular precursors, chemisorbed atoms and subsurface states. Surf. Sci.603 (10–12), 1405–1414. 10.1016/J.SUSC.2008.09.066
16
DabrowskiI. (1984). The lyman and werner bands of H2. Can. J. Phys.62 (12), 1639–1664. 10.1139/p84-210
17
FajardoM. E.TamS.DeRoseM. E. (2004) ‘Matrix isolation spectroscopy of H2O, D2O, and HDO in solid parahydrogen’, J. Mol. Struct., 695–696, pp. 111–127. 10.1016/j.molstruc.2003.11.043
18
FillionJ.-H.et al (2012). Understanding the relationship between gas and ice: Experimental investigations on ortho-para ratios. EAS Publ. Ser.58, 307–314. 10.1051/eas/1258051
19
FitzGeraldS. A.HopkinsJ.BurkholderB.FriedmanM.RowsellJ. L. C. (2010). Quantum dynamics of adsorbed normal- and para-H2, HD, and D2 in the microporous framework MOF-74 analyzed using infrared spectroscopy. Phys. Rev. B81 (10), 104305. 10.1103/PhysRevB.81.104305
20
FukutaniK.SugimotoT. (2013). Physisorption and ortho–para conversion of molecular hydrogen on solid surfaces. Prog. Surf. Sci.88 (4), 279–348. 10.1016/j.progsurf.2013.09.001
21
Gauthier-RoyB.Abouaf-MarguinL.BoisselP. (1993). Dipolar interactions between NH3 molecules trapped in solid argon. I. Kinetics of the nuclear spin species conversion. J. Chem. Phys.98 (9), 6827–6834. 10.1063/1.464774
22
HillerM.LavrovE. V.WeberJ. (2007). Ortho-para conversion of interstitial H2 in Si. Phys. Rev. Lett.98 (5), 055504. 10.1103/PhysRevLett.98.055504
23
HixsonH. G.WojcikM. J.DevlinM. S.DevlinJ. P.BuchV. (1992). Experimental and simulated vibrational spectra of H2 absorbed in amorphous ice: Surface structures, energetics, and relaxations. J. Chem. Phys.97 (2), 753–767. 10.1063/1.463240
24
IliscaE. (1991). Ortho-para H2 conversion on a cold Ag(111) metal surface. Phys. Rev. Lett.66 (5), 667–670. 10.1103/PhysRevLett.66.667
25
IliscaE.GhiglienoF. (2016). Nuclear conversion theory: Molecular hydrogen in non-magnetic insulators. R. Soc. Open Sci.3 (9), 160042. 10.1098/rsos.160042
26
IliscaE. (2018) ‘Electromagnetic nuclear spin conversion: Hydrogen on amorphous solid water’, Chem. Phys. Lett., 713, pp. 289–292. 10.1016/j.cplett.2018.10.053
27
IliscaE. (2021). Hydrogen conversion in nanocages. Hydrogen2 (2), 160–206. 10.3390/hydrogen2020010
28
KornathA.ZoermerA.KöperI. (1999) ‘Raman spectroscopic studies on matrix-isolated hydrogen and deuterium. 3. Molecular dynamics in matrices’, Spectrochimica Acta Part A Mol. Biomol. Spectrosc., 55(13), pp. 2593–2599. 10.1016/S1386-1425(99)00054-2
29
KosoneT.HoriA.NishiboriE.KubotaY.MishimaA.OhbaM.et al (2015). Coordination nano-space as stage of hydrogen ortho–para conversion. R. Soc. Open Sci.2 (7), 150006. 10.1098/rsos.150006
30
KumarS.JiangH.SchwarzerM.KandratsenkaA.SchwarzerD.WodtkeA. (2019). Vibrational relaxation lifetime of a physisorbed molecule at a metal surface. Phys. Rev. Lett.123 (15), 156101. 10.1103/PhysRevLett.123.156101
31
LavrovE. V.WeberJ. (2002). Ortho and para interstitial H2 in silicon. Phys. Rev. Lett.89 (21), 215501. 10.1103/PhysRevLett.89.215501
32
LaßK.HanX.HasselbrinkE. (2005). The surprisingly short vibrational lifetime of the internal stretch of CO adsorbed on Si(100). J. Chem. Phys.123 (5), 051102. 10.1063/1.1993550
33
LischkaM.GroßA. (2002). Hydrogen adsorption on an open metal surface: H2/Pd(210). Phys. Rev. B65 (7), 75420. 10.1103/PhysRevB.65.075420
34
MårtenssonA.-S.NybergC.AnderssonS. (1986). Observation of molecular H2 chemisorption on a nickel surface. Phys. Rev. Lett.57 (16), 2045–2048. 10.1103/PhysRevLett.57.2045
35
MiyamotoY.FushitaniM.AndoD.MomoseT. (2008) ‘Nuclear spin conversion of methane in solid parahydrogen’, J. Chem. Phys., 128(11), p. 114502. 10.1063/1.2889002
36
MorinM.LevinosN. J.HarrisA. L. (1992). Vibrational energy transfer of CO/Cu(100): Nonadiabatic vibration/electron coupling. J. Chem. Phys.96 (5), 3950–3956. 10.1063/1.461897
37
OhnoS.IvanovD.OguraS.WildeM.ArguellesE. F.DiñoW. A.et al (2018). Rotational state modification and fast ortho-para conversion of H2 trapped within the highly anisotropic potential of Pd(210). Phys. Rev. B97 (8), 085436. 10.1103/PhysRevB.97.085436
38
PengC.StavolaM.FowlerW. B.LockwoodM. (2009). Ortho-para transition of interstitial H2 and D2 in Si. Phys. Rev. B80 (12), 125207. 10.1103/PhysRevB.80.125207
39
ProchaskaF. T.AndrewsL. (1977). Vibration–rotational and pure rotational laser–Raman spectra of H2, D2, and HD in matrices at 12 K. J. Chem. Phys.67 (3), 1139–1143. 10.1063/1.434965
40
RuziM.AndersonT. D. (2013). Matrix isolation spectroscopy and nuclear spin conversion of NH3 and ND3 in solid parahydrogen. J. Phys. Chem. A117 (39), 9712–9724. 10.1021/jp3123727
41
SchmidtP. K.ChristmannK.KresseG.HafnerJ.LischkaM.GroßA. (2001). Coexistence of atomic and molecular chemisorption states: H2/Pd(210). Phys. Rev. Lett.87 (9), 096103. 10.1103/PhysRevLett.87.096103
42
ScottP. L.JeffriesC. D. (1962). Spin-lattice relaxation in some rare-earth salts at helium temperatures; observation of the phonon bottleneck. Phys. Rev.127 (1), 32–51. 10.1103/PhysRev.127.32
43
ShanJ.KleynA. W.JuurlinkL. B. F. (2009). Adsorption of molecular hydrogen on an ultrathin layer of Ni(111) hydride. Chem. Phys. Lett.474 (1–3), 107–111. 10.1016/J.CPLETT.2009.04.051
44
StulenR. H. (1988). Summary Abstract: Observation of molecular H2 and D2 on Pd and Ag using thermal desorption between 5 and 20 K. J. Vac. Sci. Technol. A6 (3), 776–778. 10.1116/1.575111
45
SugimotoT.FukutaniK. (2014). Effects of rotational-symmetry breaking on physisorption of ortho- and para-H2 on Ag(111). Phys. Rev. Lett.112 (14), 146101. 10.1103/PhysRevLett.112.146101
46
SugimotoT.FukutaniK. (2011). Electric-field-induced nuclear-spin flips mediated by enhanced spin-orbit coupling. Nat. Phys.7 (4), 307–310. 10.1038/nphys1883
47
SugimotoT.YamakawaK.ArakawaI. (2015). Infrared spectroscopic investigation of nuclear spin conversion in solid CH4. J. Chem. Phys.143 (22), 224305. 10.1063/1.4936655
48
SugimotoT.YamakawaK. (2021). Nuclear-spin conversion analysis of ν2 + ν4 combination band of crystalline methane in phase II. J. Chem. Phys.154 (2), 026101. 10.1063/5.0031272
49
SunQ.ReuterK.SchefflerM. (2004). Hydrogen adsorption on RuO2(110): Density-functional calculations. Phys. Rev. B70 (23), 235402. 10.1103/PhysRevB.70.235402
50
SvenssonK.AnderssonS. (2007). Fast ortho-para conversion of H2 adsorbed at copper surface step atoms. Phys. Rev. Lett.98 (9), 096105. 10.1103/PhysRevLett.98.096105
51
SvenssonK.BengtssonL.BellmanJ.HasselM.PerssonM.AnderssonS. (1999). Two-dimensional quantum rotation of adsorbed H2. Phys. Rev. Lett.83 (1), 124–127. 10.1103/PhysRevLett.83.124
52
TsugeM.KouchiA.WatanabeN. (2021). Measurements of ortho-to-para nuclear spin conversion of H2 on low-temperature carbonaceous grain analogs: Diamond-like carbon and graphite. Astrophysical J.923 (1), 71. 10.3847/1538-4357/ac2a33
53
TsugeM.NamiyoshiT.FuruyaK.YamazakiT.KouchiA.WatanabeN. (2021). Rapid ortho-to-para nuclear spin conversion of H2 on a silicate dust surface. Astrophysical J.908 (2), 234. 10.3847/1538-4357/abd9c0
54
TurgeonP.-A.VermetteJ.AlexandrowiczG.PeperstraeteY.PhilippeL.BertinM.et al (2017). Confinement effects on the nuclear spin isomer conversion of H2O. J. Phys. Chem. A121 (8), 1571–1576. 10.1021/acs.jpca.7b00893
55
UetaH.FukutaniK. (2023). Rotational-energy transfer in H2 ortho-paraconversion on a metal surface: Interplay between electron and phonon systems. J. Phys. Chem. Lett. 14, 7591–7596. 10.1021/acs.jpclett.3c01209
56
UetaH.SasakawaY.IvanovD.OhnoS.OguraS.FukutaniK. (2020). Direct measurement of fast ortho-para conversion of molecularly chemisorbed H2 on Pd(210). Phys. Rev. B102 (12), 121407. 10.1103/PhysRevB.102.121407
57
UetaH.WatanabeN.HamaT.KouchiA. (2016). Surface temperature dependence of hydrogen ortho-para conversion on amorphous solid water. Phys. Rev. Lett.116 (25), 253201. 10.1103/PhysRevLett.116.253201
58
WarrenJ. A.SmithG. R.GuilloryW. A. (1980). The infrared spectrum of matrix isolated hydrogen and deuterium. J. Chem. Phys.72 (9), 4901–4908. 10.1063/1.439774
59
WignerE. P. (1933). Uber die paramagnetische U mwandlung on Para-Orthowasserstoff. III. Z. Phys. Chem. B23, 28.
60
YamakawaK.AzamiS.ArakawaI. (2017). Phonon-mediated nuclear spin relaxation in H2O. Eur. Phys. J. D71 (3), 70. 10.1140/epjd/e2017-70642-8
61
YamakawaK.FukutaniK. (2020). Nuclear spin conversion of H2, H2O, and CH4 interacting with diamagnetic insulators. J. Phys. Soc. Jpn.89 (5), 051016. 10.7566/JPSJ.89.051016
62
YamakawaK.IshibashiA.NamiyoshiT.AzumaY.ArakawaI. (2020). Fast nuclear-spin conversion of H2 trapped and polarized in a CO2 matrix. Phys. Rev. B102 (4), 041401. 10.1103/PhysRevB.102.041401
Summary
Keywords
hydrogen, nuclear spin, rotational energy, adsorption, surface, matrix isolation
Citation
Ueta H, Fukutani K and Yamakawa K (2023) Fast ortho-to-para conversion of molecular hydrogen in chemisorption and matrix-isolation systems. Front. Chem. 11:1258035. doi: 10.3389/fchem.2023.1258035
Received
13 July 2023
Accepted
27 July 2023
Published
29 August 2023
Volume
11 - 2023
Edited by
Marco Sacchi, University of Surrey, United Kingdom
Reviewed by
Tomás González-Lezana, Spanish National Research Council (CSIC), Spain
Masashi Tsuge, Hokkaido University, Japan
Updates
Copyright
© 2023 Ueta, Fukutani and Yamakawa.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Koichiro Yamakawa, yamakawa.koichiro@jaea.go.jp; Hirokazu Ueta, ueta.hirokazu@jaea.go.jp
Disclaimer
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