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Comprehensive Study of Melt Infiltration for the Synthesis of NaAlH4/C Nanocomposites

机译:熔体渗透在NaAlH4/C纳米复合材料合成中的综合研究

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摘要

In the search for suitable solid state hydrogen storage systems, NaAlH4 (7.4 wt H2) holds great promise due to its suitable thermodynamical properties. However, hydrogen release and uptake are hampered by high activation energies, most likely due to solid state mass transfer limitations. A recent strategy to improve the hydrogen de- and rehydrogenation properties of NaAlH4 is to reduce the particle size to the nanometer scale. We prepared high loadings of nanosized NaAlH4 confined in the pores of a carbon support by melt infiltration. XRD, nitrogen physisorption, high pressure DSC and solid-state NMR are used to evidence that the molten NaAlH4 infiltrates the carbon support, and forms a nanosized NaAlH4 phase lacking long-range order. The confined NaAlH4 shows enhanced hydrogen dehydrogenation properties and rehydrogenation under mild conditions that is attributed to the nanosize and close contact to the carbon matrix.
机译:在寻找合适的固态储氢系统时,NaAlH4 (7.4 wt % H2) 因其合适的热力学特性而具有广阔的前景。然而,氢的释放和吸收受到高活化能的阻碍,这很可能是由于固态传质限制。最近改善 NaAlH4 的氢脱氢和再氢性能的策略是将粒径减小到纳米尺度。我们制备了高负载的纳米NaAlH4,通过熔体渗透限制在碳载体的孔隙中。采用XRD、氮气物理吸附、高压DSC和固体核磁共振等手段证明了熔融的NaAlH4渗入碳载体,并形成纳米级NaAlH4相,缺乏长程有序性。受限的NaAlH4在温和条件下表现出增强的氢脱氢性能和再氢化,这归因于纳米尺寸和与碳基体的紧密接触。

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