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Controlling the Dehydrogenation Reaction toward Reversibility of the LiBH4-Ca(BH4)2 Eutectic System

机译:LiBH4-Ca(BH4)2共晶体系的可逆脱氢反应控制

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Controlling the dehydrogenation process in a suitable reaction route by choosing the appropriate reaction conditions is crucial for a hydrogen storage system. The dehydrogenation process of the eutectic 0.68LiBH4—0.32Ca-(BH4)2 mixture was investigated by dynamic pressure-composition isotherms, X-ray diffraction, and solid-state nuclear magnetic resonance in order to determine the optimal reaction route for the dehydrogenation and to improve the hydrogen absorption reaction. In a temperature range from 330 to 450 °C, the LiBH4—Ca(BH4)2 mixture decomposes in two major steps. First, Ca(BH4)2 decomposes into CaH2, CaB6, CaB_(12)H_(12) H2, and probably amorphous boron. Second, CaH2 reacts with LiBH4 to CaB6, LiH, and H2. Li2B_(12)H_(12) has been identified as a byproduct. It was observed that the lower dehydrogenation temperature, the more CaB6 and the less [B_(12)H_(12)]~(2-) containing phases are present in the final dehydrogenation products, resulting in improved absorption performance. The temperature dependence is discussed, providing instructions to improve reversibility for potential applications and new insights into the hydrogen sorption mechanism of metal borohydrides.
机译:通过选择合适的反应条件以合适的反应路线控制脱氢过程对于氢存储系统至关重要。通过动态压力-等温等温线,X射线衍射和固态核磁共振研究了共晶0.68LiBH4-0.32Ca-(BH4)2混合物的脱氢过程,以确定最佳的脱氢反应路线。改善氢吸收反应。在330至450°C的温度范围内,LiBH4-Ca(BH4)2混合物在两个主要步骤中分解。首先,Ca(BH4)2分解为CaH2,CaB6,CaB_(12)H_(12)H2,并可能分解为无定形硼。其次,CaH2与LiBH4反应生成CaB6,LiH和H2。 Li2B_(12)H_(12)已被鉴定为副产物。观察到,最终的脱氢产物中存在较低的脱氢温度,更多的CaB6和更少的[B_(12)H_(12)]〜(2-)相,从而提高了吸收性能。讨论了温度依赖性,为提高潜在应用的可逆性提供了指导,并为金属硼氢化物的氢吸附机理提供了新见解。

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