LiBH4in Carbon Aerogel Nanoscaffolds: An NMR Study of Atomic Motions

التفاصيل البيبلوغرافية
العنوان: LiBH4in Carbon Aerogel Nanoscaffolds: An NMR Study of Atomic Motions
المؤلفون: Shane, David T., Corey, Robert L., McIntosh, Charlie, Rayhel, Laura H., Bowman, Robert C., Vajo, John J., Gross, Adam F., Conradi, Mark S.
المصدر: The Journal of Physical Chemistry - Part C; March 2010, Vol. 114 Issue: 9 p4008-4014, 7p
مستخلص: Hydrogen NMR of LiBH4in the pores of carbon aerogel nanoscaffolds shows the coexistence of motionally narrowed and broad components. The fraction of mobile, diffusing hydrogen, already evident at room temperature, increases continuously with temperature. Thus, a broad distribution of environments is present, as in some ball-milled hydrides. With decreasing pore size from 25 to 13 nm, the narrowed fraction increases, suggesting that the narrow resonance is from the most defective regions, the grain boundaries. The broad component eventually exhibits narrowing in the same temperature window as for bulk material, confirming the bulk-like structure of those regions. Hole-burning measurements reveal magnetization exchange between the broad and narrow resonance lines, confirming the close spatial proximity of the atoms in each line. The solid−solid transition is clearly evident in 7Li line shapes, with a 10−15 °C depression from the bulk. More rapid decay of the quadrupolar satellite signals in spin echoes, compared to the central transition, is due to lithium atoms diffusing between differently oriented nanocrystallites. Our results suggest that crystallites in neighboring pores have similar orientations but are incoherent for diffraction. Remarkably, the T1data of hydrogen and 7Li are continuous in the vicinity of the transition, in contrast with the bulk T1data, suggesting that some rapid lithium motion remains below the transition.
قاعدة البيانات: Supplemental Index
الوصف
تدمد:19327447
19327455
DOI:10.1021/jp9107365