Converting H+ from coordinated water into H- enables super facile synthesis of LiBH4

被引:189
作者
Chen, Kang [1 ]
Ouyang, Liuzhang [1 ]
Zhong, Hao [1 ]
Liu, Jiangwen [1 ]
Wang, Hui [1 ]
Shao, Huaiyu [2 ]
Zhang, Yao [3 ]
Zhu, Min [1 ]
机构
[1] South China Univ Technol, Guangdong Prov Key Lab Adv Energy Storage Mat, Sch Mat Sci & Engn, Guangzhou, Guangdong, Peoples R China
[2] Univ Macau, IAPME, Minist Educ, Joint Key Lab, Macau, Peoples R China
[3] Southeast Univ, Jiangsu Key Lab Adv Metall Mat, Sch Mat Sci & Engn, Nanjing, Jiangsu, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
HYDROGEN GENERATION; SODIUM-BOROHYDRIDE; LITHIUM BOROHYDRIDE; METAL-HYDRIDES; HYDROLYSIS; REGENERATION; STORAGE; NABH4; FEASIBILITY;
D O I
10.1039/c9gc01897b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
LiBH4 has excellent application potential as an off- or on-board hydrogen carrier for its unparalleled hydrogen capacity (18.5 wt%). However, the difficulty in recycling "one-pass" LiBH4 and the resulting high cost hamper its large-scale applications. Here, we report a facile and low-cost method for LiBH4 regeneration by ball milling its hydrolysis by-product (LiBO2 center dot 2H(2)O) and Mg under ambient conditions, where expensive H- stored in LiBH4 is entirely converted from cheap H+ in coordinated water. This scenario is reported for the first time without hydrides employed as hydrogen sources for the reduction process. Moreover, the yields for LiBH4 synthesized by this method may reach 40%. The cost of LiBH4 regeneration exhibits a 5-fold reduction over a previous study using NaBH4 as a raw material. Significantly, the as-purified product displays even better physicochemical properties than commercial LiBH4, for example, superior hydrolysis kinetics. Overall, a one-step approach, combining hydrogen production and storage in a closed cycle, is proposed in this work. Furthermore, the formation mechanism of LiBH4 is illustrated and the intermediate product, LiBH3(OH), is successfully observed for the first time during the regeneration course.
引用
收藏
页码:4380 / 4387
页数:8
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