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A group of researchers has identified the key stumbling block of a common solid-state hydrogen material, paving the way for future design guidelines and widespread commercial use.

Details of their findings were published in the Journal of Materials Chemistry A, where the article was featured as a Front Cover Article.

Hydrogen will play a significant role in powering our future. It's abundant and produces no harmful emissions when burned. But the storage and transportation of hydrogen is both costly and risky.

Currently, hydrogen is stored by three methods: high-pressure gaseous hydrogen storage, low-temperature liquid hydrogen storage, and solid-state hydrogen storage. Among solid-state hydrogen storage, solid-state materials are generally the safest and provide the most hydrogen storage density.

Metal hydrides have long been explored for their large hydrogen storage potentiality and their low cost. As these metals come into contact with gaseous hydrogen, hydrogen gets absorbed onto the surface. Further energy input leads to hydrogen atoms finding their way into the metal's crystal lattices until the metal becomes saturated with hydrogen. From there, the material can absorb and desorb hydrogen in larger amounts.

Magnesium hydride (MgH₂) has shown immense promise for superior hydrogen storage capacity. However, a high temperature is necessary for MgH₂ to decompose and produce hydrogen. Furthermore, the material's complex hydrogen migration and desorption, which result in sluggish dehydrogenation kinetics, have stymied its commercial application.

For decades, scientists have debated why dehydrogenation within MgH₂ is so difficult. But now, the research group has uncovered an answer.

Using calculations based on spin-polarized density functional theory with van der Waals corrections, they unearthed a 'burst effect' during MgH₂'s dehydrogenation. The initial dehydrogenation barriers measured at 2.52 and 2.53 eV, whereas subsequent reaction barriers were 0.12-1.51 eV.

The group carried out further bond analysis with the crystal orbital Hamilton population method, where they confirmed the magnesium-hydride bond strength decreased as the dehydrogenation process continued.

"Hydrogen migration and hydrogen desorption is much easier following the initial burst effect," points out Hao Li, associate professor at Tohoku University's Advanced Institute for Materials 雷速体育_中国足彩网￥在线直播 (WPI-AIMR) and corresponding author of the paper. "Structural engineering tweaks that promote this desorption process could be the key to facilitating the hydrogen desorption of MgH₂."

Li and his colleagues demonstrated that hydrogen vacancies maintained a high degree of electronic localization when the first layer of atomic hydrogen exists. Analyses of the kinetic characteristics of MgH₂ after surface dehydrogenation, performed by ab initio molecular dynamics simulations, also provided additional evidence.

"Our findings provide a theoretical basis for the MgH₂'s dehydrogenation kinetics, providing important guidelines for modifying MgH₂-based hydrogen storage materials," adds Li.

Publication Details:

Title: The "burst effect" of hydrogen desorption in MgH₂ dehydrogenation
Authors: Shuai Dong, Chaoqun Li, Jinhui Wang, Hao Liu, Zhao Ding, Zhengyang Gao, Weijie Yang, Wei Lv, Li Wei, Ying Wu, and Hao Li
Journal: Journal of Materials Chemistry A
DOI: doi.org/10.1039/D2TA06458H