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Hydrogen encapsulation in a silicon clathrate type I structure:: Na5.5(H2)2.15Si46:: Synthesis and characterization

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 129, 期 45, 页码 13857-13862

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AMER CHEMICAL SOC
DOI: 10.1021/ja0724700

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A hydrogen-encapsulated inorganic clathrate, which is stable at ambient temperature and pressure, has been prepared in high yield. Na-5.5(H-2)(2.15)Si-46 is a sodium-deficient, hydrogen-encapsulated, type I silicon clathrate. It was prepared by the reaction between NaSi and NH4Br under dynamic vacuum at 300 degrees C. The Rietveld refinement of the powder X-ray diffraction data is consistent with the clathrate type I structure. The type I clathrate structure has two types of cages where the guest species, in this case Na and H-2, can reside: a large cage composed of 24 Si, in which the guest resides in the 6d crystallographic position, and a smaller one composed of 20 Si, in which the guest occupies the 2a position. Solid-state Na-23, H-1, and Si-29 MAS NMR confirmed the presence of both sodium and hydrogen in the clathrate cages. Na-23 NMR shows that sodium completely fills the small cage and is deficient in the larger cage. The H-1 NMR spectrum shows a pattern consistent with mobile hydrogen in the large cage. Si-29 NMR spectrum is consistent with phase pure type I clathrate framework. Elemental analysis is consistent with the stoichiometry Na-5.5(H-2.15)(2)Si-46. The sodium occupancy was also examined using spherical aberration (Cs) corrected scanning transmission electron microscopy (STEM). The high-angle annular dark-field (HAADF) STEM experimental and simulated images indicated that the Na occupancy of the large cage, 6d sites, is less than 2/3, consistent with the NMR and elemental analysis.

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