Reversible hydrogen sorption in NaBH4 at lower temperatures

被引:20
作者
Chong, Lina [1 ]
Zou, Jianxin [1 ,2 ]
Zeng, Xiaoqin [1 ,2 ]
Ding, Wenjiang [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Engn Res Ctr Magnesium Mat & Applicat, Natl Engn Res Ctr Light Alloy Net Forming, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composite, Shanghai 200240, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
STORAGE MATERIALS; SYSTEM; HYDRIDES; TI; DECOMPOSITION; IMPROVEMENT; STABILITY; ADDITIVES; MECHANISM; PRESSURE;
D O I
10.1039/c3ta12369c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the present study, a new hydrogen storage system, being able to reversibly absorb/desorb hydrogen at fairly low temperatures, was developed based on a 3NaBH(4)-PrF3 composite. It is shown that 3 wt% of reversible hydrogen sorption can be achieved in the 3NaBH(4)-PrF3 composite at 400 degrees C with fast kinetics. After the addition of 5 mol% VF3, the dehydrogenation kinetics of the 3NaBH(4)-PrF3 composite can be significantly improved. The onset dehydriding temperature is lowered down to 46 degrees C in vacuum, and the dehydrogenation finishes in 2 min at 400 degrees C. Both the dehydrogenation enthalpy and activation energy of 3NaBH(4)-PrF3 can be lowered down through the addition of VF3. In particular, the dehydrogenation products of the 3NaBH(4)-PrF3-5 mol% VF3 composite can be rehydrogenated at a temperature as low as 48 degrees C with the regeneration of NaBH4. At 84 degrees C, a reversible hydrogen sorption of about 1.2 wt% can be achieved in the 3NaBH(4)-PrF3-5 mol% VF3 composite. The improvement in hydrogen sorption properties can be mainly attributed to the formation of the VB2 phase during dehydrogenation as an efficient catalyst, which maintains well its catalytic effect in the re-/dehydrogenation cycles. Based on a series of controlled experiments and phase analyses, the de-/rehydrogenation mechanisms of the 3NaBH(4)-PrF3 composite without and with VF3 addition are proposed and discussed in detail.
引用
收藏
页码:13510 / 13523
页数:14
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