Recently, the kinetic improvement of the nitrogenation reaction of lithium hydride (LiH) to form lithium imide (Li
2NH) by adding a scaffold was reported. The scaffold prevents agglomeration of Li
2NH and maintains the activity of LiH, achieving a reduction in
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Recently, the kinetic improvement of the nitrogenation reaction of lithium hydride (LiH) to form lithium imide (Li
2NH) by adding a scaffold was reported. The scaffold prevents agglomeration of Li
2NH and maintains the activity of LiH, achieving a reduction in reaction temperature and an increase in reaction rate. In this work, a Li–Si alloy, Li
22Si
5, was used as a starting material to form nano-sized LiH dispersed in a Li alloy matrix. Lithium nitride (Li
3N) is generated by the reaction between Li
22Si
5 and N
2 to form Li
7Si
3, and then Li
3N is converted to LiH with ammonia (NH
3) generation during heat treatment under H
2 flow conditions. Since Li
3N is formed at the nano-scale on the surface of alloy particles, LiH generated from the above nano-Li
3N is also nano-scale. The differential scanning calorimetry results indicate that direct nitrogenation of LiH in the alloy matrix occurred from around 280 °C, which is much lower than that of the LiH powder itself. Such a highly active state might be achieved due to the nano-crystalline LiH confined by the Li alloy as a self-transformed scaffold. From the above experimental results, the nano-confined LiH in the alloy matrix was recognized as a potential NH
3 synthesis technique based on the LiH-Li
2NH type chemical looping process.
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