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Revisiting the Hydrogen Storage Behavior of the Na-O-H System

机译:回顾Na-O-H系统的储氢行为

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摘要

Solid-state reactions between sodium hydride and sodium hydroxide are unusual among hydride-hydroxide systems since hydrogen can be stored reversibly. In order to understand the relationship between hydrogen uptake/release properties and phase/structure evolution, the dehydrogenation and hydrogenation behavior of the Na-O-H system has been investigated in detail both ex- and in-situ. Simultaneous thermogravimetric-differential thermal analysis coupled to mass spectrometry (TG-DTA-MS) experiments of NaH-NaOH composites reveal two principal features: Firstly, an H2 desorption event occurring between 240 and 380 °C and secondly an additional endothermic process at around 170 °C with no associated weight change. In-situ high-resolution synchrotron powder X-ray diffraction showed that NaOH appears to form a solid solution with NaH yielding a new cubic complex hydride phase below 200 °C. The Na-H-OH phase persists up to the maximum temperature of the in-situ diffraction experiment shortly before dehydrogenation occurs. The present work suggests that not only is the inter-phase synergic interaction of protic hydrogen (in NaOH) and hydridic hydrogen (in NaH) important in the dehydrogenation mechanism, but that also an intra-phase Hδ+… Hδ– interaction may be a crucial step in the desorption process.
机译:在氢化物-氢氧化物体系中,氢化钠与氢氧化钠之间的固态反应不常见,因为氢可以可逆地存储。为了理解氢吸收/释放性质与相/结构演变之间的关系,已对Na-O-H系统的脱氢和氢化行为进行了详细的现场和非现场研究。 NaH-NaOH复合材料的同时热重差热分析与质谱(TG-DTA-MS)实验相结合揭示了两个主要特征:首先,H2解吸事件发生在240至380°C之间,其次是在170左右的吸热过程°C,无相关重量变化。原位高分辨率同步加速器粉末X射线衍射显示,NaOH似乎与NaH形成固溶体,在200°C以下产生新的立方配合物氢化物相。在发生脱氢之前不久,Na-H-OH相一直保持到原位衍射实验的最高温度。目前的研究表明,不仅质子氢(NaOH)和氢化氢(NaH)的相间协同作用在脱氢机理中很重要,而且相内H δ+ …H δ– 相互作用可能是解吸过程中的关键步骤。

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