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Reaction Behavior of the Li-N-H Hydrogen Storage System with Boron Nitride as an Additive

机译:Li-N-H储氢体系与氮化硼作为添加剂的反应行为

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摘要

This work begins with a discussion of the desorption, reaction rate-limiting step of a LiNH2-LiH hydrogen storage system. Using microstructural and thermodynamic studies, it explains the working mechanism of BN as an additive in Li-N-H hydrogen storage materials. High-energy wet ball milling with THF was applied to the LiNH2 + 1.2LiH mixture. The results obtained in this work show that the rate-limiting step of the desorption reaction depends on the degree of oxidation and amount of LiH in the system. The activation energy of the desorption reaction of both ball-milled LiNH2 and LiNH2 + 1.2LiH samples was reduced with BN as an additive. BN had no clear impact on the crystallite sizes of LiNH2 + 1.2LiH as-milled samples. However, it was found that BN stabilizes the crystallite sizes of LiNH2 + 1.2LiH samples during the high-temperature desorption and absorption processes.
机译:这项工作首先讨论LiNH2-LiH储氢系统的解吸,反应速率限制步骤。通过微观结构和热力学研究,它解释了BN作为Li-N-H储氢材料中添加剂的工作机理。将具有THF的高能湿式球磨应用于LiNH2 + 1.2LiH混合物。这项工作获得的结果表明,解吸反应的限速步骤取决于系统中氧化程度和LiH量。使用BN作为添加剂可以降低球磨LiNH2和LiNH2 + 1.2LiH样品的解吸反应的活化能。 BN对研磨后的LiNH2 + 1.2LiH的微晶尺寸没有明显影响。然而,发现在高温解吸和吸收过程中,BN使LiNH2 + 1.2LiH样品的微晶尺寸稳定。

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