International Conference on Gas Hydrates (ICGH) (6th : 2008)

MIGRATION OF HYDROGEN GUEST MOLECULES THROUGH CLATHRATE CAGES. Alavi, Saman; Ripmeester, John A. Jul 31, 2008

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MIGRATION OF HYDROGEN GUEST MOLECULES THROUGH CLATHRATE CAGES  Saman Alavi∗ Department of Chemistry, University of Ottawa, Ottawa, ON, K1N 6N5, CANADA  John Ripmeester The Steacie Institute for Molecular Sciences, National Research Council of Canada 100 Sussex Drive, Rm 111, Ottawa, Ontario, K1A OR6, CANADA   ABSTRACT Electronic structure calculations are performed to determine the barriers to migration of molecular hydrogen in clathrate cages. The barriers are used in a chemical reaction rate expression to determine the rate of H2 migration and the diffusion coefficient for the hydrogen guest molecules. Calculations are performed for migration of hydrogen guests through pentagonal and hexagonal clathrate cage faces. Cage faces where the water molecules obey the water rules and cage faces with Bjerrum L and D defects are considered. The migration barriers were calculated to be ≈25 kcal/mol from the pentagonal faces and between 5 to 6 kcal/mol for the hexagonal faces, depending on the orientation of the hydrogen molecule.  Keywords: gas hydrates, hydrogen storage, hydrogen migration kinetics   ∗ Corresponding author: Phone: +1 613 265 5335 Fax +1 613 998 7833 E-mail: saman.alavi@nrc-cnrc.gc.ca NOMENCLATURE A(T) Arrhenius pre-exponential factor [s-1] E0 activation barrier to guest migration [kcal mol-1] Dself diffusion coefficient of guest molecule [m s-2] ktot total migration rate constant [s-1] kclass classical transition state theory migration rate constant [s-1] ℓ tunneling length V(x) potential energy profile for guests inside clathrate cages [kcal mol-1] κ tunneling correction to migration rate constant λ hop distance for diffusion [m] νs imaginary frequency corresponding to the tunneling barrier [s-1] τ  hopping time [s]  INTRODUCTION Pure hydrogen and deuterium structure II (sII) clathrates and mixed hydrogen / tetrahydrofuran (THF) sII clathrates have been suggested as materials for hydrogen storage. In addition to the capacity of these materials for hydrogen gas storage under different temperature and pressure conditions, the stability of the guest H2 molecules in the clathrate structure must be established. Experimentally, it is possible to determine the stability of the hydrogen clathrate by following the guest Raman and/or NMR peak intensities over long periods of time. Theoretically, the stability of H2 guests in the clathrate cages can be determined by a study of the migration rates of the guests between the clathrate cages. In this work, we use electronic structure calculations to estimate the energy barriers to the diffusion of hydrogen guest molecules through pentagonal and hexagonal clathrate cage faces. Specifically, we study the diffusion of the H2 through a pentagonal face of a dodecahedral 512 clathrate cage and a hexagonal face of a hexakaidecahedral 51264 clathrate cage. The barrier to diffusion through the faces will be determined for H2 guest orientations perpendicular and parallel to each face. The calculations are performed at the B3LYP levels with the large 6-311++G(d,p) basis set. The energy barriers and profiles are used to estimate escape rates from the cages using a simple Arrhenius expression. Quantum mechanical tunneling contributions to the escape rate are also considered. These studies indicate that hydrogen migration through clathrates can occur and kinetic considerations can be very important in determining the structure and hydrogen storage capacity of clathrates. Proceedings of the 6th International Conference on Gas Hydrates (ICGH 2008), Vancouver, British Columbia, CANADA, July 6-10, 2008. The pure sII hydrogen clathrate can be synthesized at  pressures between 180 to 600 MPa for temperatures near room temperature.[1,2] The hydrogen clathrate is kinetically stable at 1 bar for temperatures lower than 140 K.[3] The cubic sII Fd3m space group has a unit cell with 136 water molecules composed of a framework with sixteen dodecahedral cages with pentagonal faces (512) and a cavity radius of 3.91 Å. The unit cell has eight hexakaidecahedral cages, with twelve pentagonal and four hexagonal faces (51264) arranged in tetrahedral geometry about the cage centre.[4] The cavity radius of the large cages is 4.73 Å.[5] The experimental stoichiometric ratio of H2 to H2O in the clathrate is determined to be 0.35-0.48 which indicates multiple hydrogen guest occupancies of the cages. The occupancy of the large cages in the hydrogen and deuterium clathrates are considered to be four.[1],[6] Direct microscopic volumetric measurements and Raman vibron intensities indicate[1] the double occupancy of the small cages, however, separate models derived from neutron diffraction studies of the D2 sII clathrate[6] suggest that the small cages are only singly occupied. The occupancies of the cages are observed to decrease as the temperature of the clathrate is raised. The binary sII H2+THF clathrate can be synthesized at lower pressures (15 MPa) with the THF molecules occupying the large cages and the H2 molecules occupy the small sII clathrate cages.[7] The small cages in the binary clathrate have been assigned single occupancy (or lower) to hydrogen in the small cages,[7-9] but studies with non-stoichiometric THF sII clathrates shown evidence of double occupancy[10] of the small cages by H2. Experimental and computational[11,12] work performed to-date implicitly assume that the occupancies of the cages in H2 or H2+THF clathrates remain constant over time. There is experimental and computational[13] evidence that the occupancies of the small cages in sII H2+THF clathrates change over a time scale of hours to days, even at low temperatures. We calculate the barrier and rate of escape of hydrogen molecules from faces of the small and large clathrate cages. High migration and quantum mechanical tunnelling rates of the hydrogen guests would show the need to revisit the interpretations of previous experiments. In our calculations, experimental X-ray crystallography of the sII clathrate unit cell[4] is used to determine the positions of the water oxygen atoms. The disordered hydrogen atoms of the water molecules are attached to the oxygen atoms in a manner consistent with the ice rules. An isolated small and large cage were selected from this unit cell. The hydrogen guest molecules are placed at the center of small and large sII clathrate cages and moved towards the center of chosen pentagonal or hexagonal faces. Parallel and perpendicular orientations of the H2 guest axis are maintained as it is moved towards the face. The initial and final placements of the hydrogen molecule in the small and large cages are shown in Figure 1. The cages and hydrogen guest molecule were considered rigid in determining the energy of the configurations and ten placements between the center of the cage and the center of the face were considered to obtain a smooth energy profile for the guest in the cage.                Figure 1. The sII small and large cages with the H2 guest molecule in the center of the cage and in the center of a pentagonal or hexagonal faces. The energy of the hydrogen in the small cage was calculated for ten points between these two limits. The cage atoms and bond length of the H2 guest were considered fixed.  The energy as a function of the distance of the hydrogen guest centre of mass from the centre of the large sII clathrate cage is shown in Figure 2. The energy was determined from electronic structure calculations with Gaussian 98[14] at the B3LYP level with the 6-311++G(d,p) basis set. The energy profile for guest migration was determined after introducing L- and D-type Bjerrum defects in the faces. These profiles are also shown in Figure 2.  A similar profile for the H2 migration through a pentagonal face of a small sII cages is shown in Figure 3.                  Figure 2. The energy profile for hydrogen guest migration through a pentagonal face of a small cage for orientations shown in Fig. 1.                   Figure 3. The energy profile for hydrogen guest migration through a hexagonal face of a large cage for orientations shown in Fig. 1.  The energy required for the H2 guest to migrate through a hexagonal face of a large cage is between 5 to 6.5 kcal/mol. The energies of the perpendicular configuration (left panel of Fig.1) are smaller than the parallel configuration (right panel of Fig.1). The L-type Bjerrum defects in a face decrease the barrier heights considerably. The barrier to migration through the smaller pentagonal faces of the small cages are much larger and between 23 and 29 kcal/mol, depending on the orientation of the hydrogen molecule and the presence of defects. In reality, due to molecular rotation, the hydrogen guests are effectively spherical and the barriers to migration through the cages will lie in between values determined for the two limiting orientations. The total rate constant for the migration of hydrogen through these barriers, ktot(T), can be estimated by a classical transition state theory (TST) expression, kclass(T), and the quantum mechanical tunnelling correction, κ(T),[15] ktot(T) =  κ(T) kclass(T).  (1) The shape of the tunneling barrier is determined by the energy profile shown in Fig. 2. Since migration takes the H2 guest to a similar cage, the barrier is symmetric about the highest point and the energy profiles of Fig. 2 are fit to the one- dimensional Eckart sech2 model,[16] [ ]2 0 )/2exp(1 )/2exp(4 )( l l x xE xV π π +=   (2) where E0 is the migration barrier and ℓ is a characteristic length related to the magnitude of the imaginary frequency corresponding to the tunneling barrier, |νs|. Using the guest reduced mass, μ it can be shown that, μν 2 02 2l E s = .   (3) The calculated energy profile shows a good fit to the functional form of Eq. (2) and the corresponding Eckart potential parameters for the cases studied in this work are given in Table 1.  Cage (orientation) E0 / kcalmol-1 ℓ / Å  νs /  1012 s-1 Small cage, ⊥ (S) L-defect, ⊥ (S) D-defect, ⊥ Small cage, || (S) L-defect, || (S) D-defect, || Large cage, ⊥ (L) L-defect, ⊥ (L) D-defect, ⊥ Large cage, || (L) L-defect, || (L) D-defect, || 24.1 22.4 24.7 29.1 26.6 30.1 5.8 5.7 5.6 7.1 6.6 5.1 3.26 2.99 3.38 3.09 2.68 3.12 3.35 3.20 3.50 3.92 3.49 3.30 15.330 16.118 14.972 17.774 19.621 17.923 7.339 7.573 6.981 6.926 6.984 7.486 Table 1. The Eckart potential parameters for the tunneling barrier to hydrogen migration. The S or L signifies the small or large cage.  ⊥ L-Defect ⊥ ⊥ D-Defect || L-Defect || || D-Defect  || L-Defect || || D-Defect ⊥ L-Defect ⊥ ⊥ D-Defect  The tunneling correction at each temperature is determined from, .)( ⎟⎟⎠ ⎞ ⎜⎜⎝ ⎛ ++= 0 2 1 24 11 E kT kT hT sνκ   (4) The Eckart model parameters are used to calculate the tunneling corrections at different temperatures by using Eq. (4). The classical rate constant of hydrogen migration, kclass, is calculated with a simple transition state theory expression, kclass(T) = A(T)exp(−E0/RT),  (5) where A(T) is the Arrhenius pre-exponential factor (s-1) which is related to the rattling frequency of the hydrogen guests in the small and large cages, and E0 is the activation barrier to migration. The frequency of rattling motion of hydrogen in the small and large cages was determined by molecular dynamics calculations. The Fourier transforms of the normalized velocity autocorrelation function, 〈v(t)·v(0)〉/〈v(0)·v(0)〉, for the center of mass of the hydrogen molecules in the large and small cages were used to calculate the vibrational frequencies and periods. As expected, the hydrogen guests in the small cages have a higher rattling frequency (~3 THz) than those in the large cages (~1.5 THz). These frequencies are used as estimates for the pre- exponential factor, A, in the TST expression for the classical rate constant given in Eq. (5). The total rate constants for migration of H2 guests through in the hexagonal and pentagonal faces are shown in Figs. 4 and 5, respectively. Figure 4. The total rate constant for migration of molecular hydrogen through the hexagonal faces of sII large cages.  The rate constant for the migration of hydrogen from the large cages is roughly four orders of magnitude larger than the rate constants for migration from the small cages.  Figure 5. The total rate constant for migration of molecular hydrogen through the pentagonal faces of sII small cages.  In the jump-diffusion model,[16,17] the self- diffusion coefficient, Dself is determined from the shortest hop distance λ, and the time interval between two hops, τ, Dself = λ2 / 6τ.  (6) The hop distance in the clathrates is the distance of the centers of neighboring small or large cages and the hopping time is the inverse of the rate constant for the hydrogen migration, τ = 1/ ktot(T). The diffusion coefficients of the H2 guests in the large cages in this model are comparable smaller O(10-10 m2/s) than diffusion coefficients measured for H2 in zeolites which are O(10-8 m2/s).[17] The migration rates and diffusion coefficients calculated in this work are lower limits to the experimental migration rates. The cages and H2 molecules are considered to be rigid. Recent computational studies of the diffusion of H2 in the silica zeolite sodalite[18] show that cage flexibility allows the opening of the polyhedral faces through which the hydrogen guests diffuse and this leads to a substantial decrease in the energy barrier to migration. Presumably, allowing flexibility in the clathrate cages would also decrease the energy barrier to hydrogen migration, thus increasing the rate of migration and the diffusion coefficient of the hydrogen guests. To our knowledge experimental measurements of the migration of H2 in the sII clathrates have not been published. A direct molecular dynamics calculation of the migration rate would account for the flexibility of the cages, the effects of multiple occupancies of the cages on the rattling frequencies and barrier heights of the guests, the external pressure, and the possibility of Bjerrum defects modifying the tunnelling barriers. In ice lattices and clathrates, Bjerrum defects are formed in the same temperature region as guest migration and have an activation barrier of 6-15 kcal/mol.[18] In the clathrate hydrates, barriers to the formation of Bjerrum defects, as judged from the reorientational dynamics of water molecules are guest-dependent. As seen in Figures 4 and 5, these defects decrease the energy barrier to migration through the faces of the polyhedra. ⊥ ⊥⊥ ⊥ ⊥ ⊥ The quantum mechanical translation / rotation eigenvalues and eigenstates of H2 in the small sII clathrate cage show that at temperatures above 150 K, the translational motion of hydrogen inside the cage is predominantly classical.[19] The zero-point energies of each hydrogen molecule in the small cages are ≈2 kcal/mol. This zero-point energy decreases the effective energy required to pass over the diffusion barrier and will increase the rate of migration compared to the values calculated in this work.  Our calculations show that the rate of hydrogen migration, especially through large cages at temperatures above 150 K can be considerable. In the small cages, the rates of migration are much smaller. Hydrogen migration is also expected to occur from the large cages of sH and sI clathrates since the size of the hexagonal faces in these clathrates are comparable with the hexagonal faces of the sII large cages. The large cages of sI, sII and sH clathrates are also coupled to the small cages through pentagonal faces. The diffusion through these faces should be comparable to that of hydrogen migration through the small cages.  REFERENCES [1] Rehman S. Solar radiation over Saudi Arabia and comparisons with empirical models. Energy 1998;23(12):1077-1082. [2] Gumz W. Gas producers and blast furnaces. New York: John Wiley and Sons Inc., 1950. [3] Tribus M, Evans RB. A contribution to the theory of thermoeconomics, report no. 62-36. Los Angeles, CA: UCLA Engineering Department, 1962. [4] Sintak Y. Models and projections of energy use in the Soviet Union. In: Steiner T, editor. International Energy Economics. London: Chapman and Hall, 1970. p. 1-53.  [1] Mao WL, Mao HK, Goncharov AF, Struzhkin VV, Guo Q, Hu J, Shu J, Hemley RJ, Somayazulu M, Zhao Y. Hydrogen clusters in clathrate hydrate. Science, 2002, 297, 2247-2249. [2] Dyadin YA, Larianov EG, Manakov AY, Zhurkov FV, Aladko EY, Mikina TV, Komarov VY. Clathrate hydrates of hydrogen and neon. Mendeleev Commun. 1999, 9; 209-210. [3] Mao WL, Mao HK. Hydrogen storage in molecular compounds. Proc. Nat. Acad. Sci. 2004, 101, 708-710. [4] Mak TC, McMullan RK. Polyhedral clathrate hydrates. X. Structure of the double hydrate of tetrahydrofuran and hydrogen sulfide. J. Chem. Phys. 1965, 42; 2732-2737. [5] Sloan ED. Fundamental principles and applications of natural gas hydrates. Nature (London) 2003, 426; 353-359. [6] Lokshin KA, Zhao Y, He D, Mao WL, Mao HK, Hemley RJ, Lobanov MV, Greenblatt M. Structure and dynamics of hydrogen molecules in the novel clathrate hydrate by high pressure neutron diffraction. Phys. Rev. Lett. 2004, 93; 125503-1-125503-4. [7] a) L. J. Florusse, C. J. Peters, J. Schoonman, K. C. Hester, C. A. Koh, S. F. Dec, K. N. Marsh, E. D. Sloan. Stable low-pressure hydrogen clusters stored in binary clathrate hydrate. Science 2004, 306; 469-471; b) Hashimoto S, Murayama S, Sugahara T, Sato H, Ohgaki K. Thermodynamic and Raman spectroscopic studies on H2 + tetrahydrofuran + water and H2 + tetra-n-butyly ammonium bromide + water mixtures containing gas hydrates. Chem. Eng. Sci. 2006, 61; 7884- 7888. [8] Strobel TA, Taylor CJ, Hester KC, Dec SF, Koh CA, Miller KT, Sloan Jr. ED. Molecular hydrogen storage in binary THF-H2 clathrate hydrates. J. Phys. Chem. B  2006, 110; 17121- 17125. [9] Hester KC, Strobel TA, Sloan ED, Koh CA, Huq A, Schulz AJ. Molecular hydrogen occupancy in binary THF-H2 clathrate hydrates by high resolution neutron diffraction. J. Phys. Chem. B 2006, 110; 14024-14027. [10] Lee H, Lee JW, Kim DY, Park J, Seo YT, Zeng H, Moudrakovski IL, Ratcliffe CI, Ripmeester JA. Tuning clathrate hydrates for hydrogen storage. Nature 2005, 434; 743-746. [11] a) Sluiter MHF, Belosludov RV, Jain A, Belosludov VR, Adachi H, Kawazoe Y, Higuchi K, Otani T. Ab initio study of hydrogen clathrate hydrates for hydrogen storage within the ITBL environment. Lect. Notes Comput. Sci. 2003, 2858, 330-341; Sluiter MHF, Adachi H, Belosludov RV, Belosludov VR, Kawazoe Y. Ab initio study of hydrogen storage in hydrogen clathrate hydrates. Mater. Trans. 2004, 45; 1452- 1454; b) T. M. Inerbaev, V. R. Belosludov, R. V. Belosludov, M. H. F. Sluiter, Y. Kawazoe. Dynamics and equation of state of hydrogen clathrate hydrate as a function of cage occupation. Comput. Mater. Sci. 2006, 36; 229-233. [12] a) Alavi S, Ripmeester JA, Klug DD. Molecular dynamics study of structure II hydrogen clathrates. J. Chem. Phys. 2005, 123; 024507-1- 024507-7; b) Alavi S, Ripmeester JA, Klug DD. Molecular dynamics simulations of binary structure II hydrogen and tetrahydrofuran clathrates. J. Chem. Phys. 2006, 124; 014704-1- 014704-6; c) Alavi S, Ripmeester JA, Klug DD. Molecular dynamics simulations of binary structure H hydrogen and methyl-tert-butylether clathrate hydrates. J. Chem. Phys. 2006, 124; 204707-1-204707-8. [13] Frankcombe TJ, Kroes G-J. Molecular dynamics simulations of type-sII hydrogen clathrate hydrates close to equilibrium conditions. J. Phys. Chem. C 2007, 111, 13044-13052. [14] Gaussian 98, Revision A.11.3, Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Zakrzewski JA, Montgomery Jr. JA, Stratmann RE, Burant JC, Dapprich S, Millam JM, Daniels AD, Kudin KN, Strain MC, Farkas O, Tomasi J, Barone V, Cossi M, Cammi B, Mennucci B, Pomelli C, Adamo C, Clifford S, Ochterski JW,  Petersson GA, Ayala PY, Cui Q, Morokuma K, Rega N, Salvador P, Dannenberg JJ, Malick DK, Rabuck AD, Raghavachari K, Foresman JB, Cioslowski J, Ortiz JV, Baboul AG, Stefanov BB, Liu G, Liashenko A, Piskorz P, Komaromi I, Gomperts R, Martin RL, Fox DJ, Keith T, Al-Laham MA, Peng CY, Nanayakkara A, Challacombe M, Gill PMW, Johnson B, Chen W, Wong MW, Andres JL, Gonzalez C, Head- Gordon M, Replogle ES, Pople JA, Gaussian, Inc., Pittsburgh PA, 2002. [15] a) Steinfeld JI, Francisco JS, Hase HW. Chemical Kinetics and Dynamics. Englewood Cliffs, NJ:  Prentice-Hall, 1989. [16] a) Eckart C. The penetration of a potential barrier by electrons. Phys. Rev. 1930, 35; 1303- 1309; b) Johnston HS, Heicklen J. Tunnelling corrections for unsymmetrical Eckart potential energy barriers. J. Phys. Chem. 1962, 66; 532- 533. [17] Bär NK, Ernst H, Jobic H, Kärger J. Combined quasi-elastic neutron scattering and NMR study of hydrogen diffusion in zeolites. Magn. Res. Chem. 1999, 37; S79-S83. [18] a) van den Berg AWC, Bromley ST, Ramsahye N, Maschmeyer T. Diffusion of molecular hydrogen through porous materials: the importance of framework flexibility. J. Phys. Chem. B 2004, 108; 5088-5094; b) van den Berg AWC, Bromley ST, Flikkema E, Wojdel J, Maschmeyer T, Jansen JC. Molecular-dynamics analysis of the diffusion of molecular hydrogen in all-silica sodalite. J. Chem. Phys. 2004, 120; 10285-10289. [19] Xu M, Elmatad YS, Sebastianelli F, Moskowitz JW, Bačić Z. Hydrogen molecule in small dodecahedral cage of a clathrate hydrate: Quantum five-dimensional calculations of the coupled translation-rotation eigenstates. J. Phys. Chem. B 2006, 110; 24806-24811.  

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