4.6 Article

Kinetic alteration of the 6Mg(NH2)2-9LiH-LiBH4 system by co-adding YCl3 and Li3N

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 19, Issue 47, Pages 32105-32115

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cp06826c

Keywords

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Funding

  1. CAS-HZG collaborative project RevHy - Study on the synthesis, structures and performances of complex hydrides systems for Reversible high capacity Hydrogen storage at low temperatures
  2. project HySCORE - Hydride & Polymer Foils: Efficient H2 storage by means of novel hierarchical porous shell structures Embedded light metal hydrides [03SF0532B]
  3. Helmholtz Foundation
  4. European Marie Curie Actions under ECOSTORE grant [607040]
  5. CONICET (Consejo Nacional de Invetigaciones Cientificas y Tecnicas)
  6. ANPCyT - (Agencia Nacional de Promocion Cientifica y Tecnologica)
  7. CNEA (Comision Nacional de Energia Atomica)

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The 6Mg(NH2)(2)-9LiH-LiBH4 composite system has a maximum reversible hydrogen content of 4.2 wt% and a predicted dehydrogenation temperature of about 64 degrees C at 1 bar of H-2. However, the existence of severe kinetic barriers precludes the occurrence of de/re-hydrogenation processes at such a low temperature (H. Cao, G. Wu, Y. Zhang, Z. Xiong, J. Qiu and P. Chen, J. Mater. Chem. A, 2014, 2, 15816-15822). In this work, Li3N and YCl3 have been chosen as co-additives for this system. These additives increase the hydrogen storage capacity and hasten the de/re-hydrogenation kinetics: a hydrogen uptake of 4.2 wt% of H-2 was achieved in only 8 min under isothermal conditions at 180 degrees C and 85 bar of H-2 pressure. The re-hydrogenation temperature, necessary for a complete absorption process, can be lowered below 90 degrees C by increasing the H-2 pressure above 185 bar. Moreover, the results indicate that the hydrogenation capacity and absorption kinetics can be maintained roughly constant over several cycles. Low operating temperatures, together with fast absorption kinetics and good reversibility, make this system a promising on-board hydrogen storage material. The reasons for the improved de/re-hydrogenation properties are thoroughly investigated and discussed.

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