Reversibility of LiBH4 Facilitated by the LiBH4-Ca(BH4)2 Eutectic

Payam Javadian, SeyedHosein Payandeh GharibDoust, Haiwen Li, Drew A. Sheppard, Craig E. Buckley, Torben R. Jensen

研究成果: Contribution to journalArticle査読

12 被引用数 (Scopus)

抄録

The hydrogen storage properties of eutectic melting 0.68LiBH4–0.32Ca(BH4)2 (LiCa) as bulk and nanoconfined into a high surface area, SBET = 2421 ± 189 m2/g, carbon aerogel scaffold, with an average pore size of 13 nm and pore volume of Vtot = 2.46 ± 0.46 mL/g, is investigated. Hydrogen desorption and absorption data were collected in the temperature range of RT to 500 °C (ΔT/Δt = 5 °C/min) with the temperature then kept constant at 500 °C for 10 h at hydrogen pressures in the range of 1–8 and 134–144 bar, respectively. The difference in the maximum H2 release rate temperature, Tmax, between bulk and nanoconfined LiCa during the second cycle is ΔTmax ≈ 40 °C, which over five cycles becomes smaller, ΔTmax ≈ 10 °C. The high temperature, Tmax ≈ 455 °C, explains the need for high temperatures for rehydrogenation in order to obtain sufficiently fast reaction kinetics. This work also reveals that nanoconfinement has little effect on the later cycles and that nanoconfinement of pure LiBH4 has a strong effect in only the first cycle of H2 release. The hydrogen storage capacity is stable for bulk and nanoconfined LiCa in the second to the fifth cycle, which contrasts to nanoconfined LiBH4 where the H2 storage capacity continuously decreases. Bulk and nanoconfined LiCa have hydrogen storage capacities of 5.4 and 3.7 wt % H2 in the fifth H2 release, which compare well with the calculated hydrogen contents of LiBH4 only and in LiCa, which are 5.43 and 3.69 wt % H2, respectively. Thus, decomposition products of Ca(BH4)2 appear to facilitate the full reversibility of the LiBH4, and this approach may lead to new hydrogen storage systems with stable energy storage capacity over multiple cycles of hydrogen release and uptake.
本文言語英語
ページ(範囲) 18439–18449
ジャーナルJournal of Physical Chemistry C
121
DOI
出版ステータス出版済み - 2017

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