Rare-Earth Metal Trigger Enhanced Generation Kinetics of Lithium Borohydride

动力学 稀土 锂(药物) 硼氢化 金属 化学 无机化学 土(古典元素) 金属锂 材料科学 矿物学 催化作用 物理化学 有机化学 电极 医学 物理 量子力学 电解质 数学物理 内分泌学
作者
Yongyang Zhu,Qing Zhou,Liming Zeng,Daifeng Wu,Renheng Tang,Shun Wang
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:12 (28): 10537-10543 被引量:5
标识
DOI:10.1021/acssuschemeng.4c02943
摘要

The lack of efficient and economic synthesis techniques for LiBH4 limits its popularization as a high-capacity hydrolysis material to supply hydrogen for fuel cells. Reversibly converting the low-cost hydrolytic products, typically hydrated lithium borate (LiBO2·xH2O), into LiBH4 via Mg reductants appears attractive, bringing the hope to realize a closed loop for LiBH4 hydrolysis and regeneration; however, the strong B–O bonds in LiBO2·xH2O and the weak reducing capacity pose a severe kinetics obstacle with low yield. Herein, we propose an optimized method to produce LiBH4 by facile ball milling under ambient conditions, with Li2B4O7·3H2O and LiOH·H2O as reactants, Mg-RE that was obtained by introducing cheap rare-earth metals (RE) to normal Mg as reductants, and minor MgH2 as reaction triggers and supplementary hydrogen sources. The usage of Mg-RE can not only improve the contacting efficiency between reactants due to its grind-aiding induced by hard and brittle features but also empower the reducing ability, since the H-philic nature of RE makes Mg-RE prone to hydrogenation, in situ forming highly active intermediate phases that accelerate the conversion of initial H+ to H–. A high LiBH4 yield of 33% can thus be achieved in a relatively short ball milling time of 10 h. This work enriches the synthesis pathways of LiBH4 and boosts its competitiveness for scaled applications.
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