近期，我院研究生贾凯、教师吴富英（共一）、陈代芬（通讯）、张刘挺（通讯）等的研究成果“Elastic Framework Driven Mg2+ Autocapture and Autocatalysis: Mechanistic Origin of Fast Hydrogen Release in 2LiBH4-MgH2”在《Rare Metals》（一区TOP，IF=11）上发表。

近期，我院研究生贾凯、教师吴富英（共一）、陈代芬（通讯）、张刘挺（通讯）等的研究成果“Elastic Framework Driven Mg²⁺ Autocapture and Autocatalysis: Mechanistic Origin of Fast Hydrogen Release in 2LiBH₄-MgH₂”在《Rare Metals》（一区TOP，IF=11）上发表。

论文简介如下：

The protracted incubation time has long been the Achilles’ heel of the promising 2LiBH₄–MgH₂ hydrogen storage system. Instead of the usual route-creating heterogeneous nucleation sites to hasten MgB₂ formation-we shortened both de- and re-hydrogenation incubation periods by steering the Mg transformation itself. Herein, this paper engineered a Prussian-blue analogue whose surface charge landscape traps Mg²⁺ and the released electrons in a non-stoichiometric lattice, keeping them instantly available for MgB₂ nucleation. Theory and experiment show that CoFe-PBA stores both ion and electron; Under the same experimental temperature, the optimized LiBH₄-MgH₂ hydrogen storage system demonstrates remarkable performance improvements: its incubation period is significantly reduced to just one seventh that of the original hydrogen storage material, achieving a leap forward in reaction kinetics efficiency. The above concept provides a versatile tool for any catalytic system constrained by nucleation delays and opens new avenues for energy-related research.