Balcerzak Mateusz, Ponsoni Jéssica Bruna, Petersen Hilke, Menéndez César, Ternieden Jan, Zhang Linda, Winkelmann Frederik, Aguey-Zinsou Kondo-Francois, Hirscher Michael, Felderhoff Michael
Heterogeneous Catalysis Department, Max-Planck-Institut für Kohlenforschung, Mülheim an der Ruhr 45470, Germany.
Institute of Materials Science and Engineering, Poznan University of Technology, Poznan 61-138, Poland.
J Am Chem Soc. 2024 Feb 28;146(8):5283-5294. doi: 10.1021/jacs.3c11943. Epub 2024 Feb 14.
The research on the functional properties of medium- and high-entropy alloys (MEAs and HEAs) has been in the spotlight recently. Many significant discoveries have been made lately in hydrogen-based economy-related research where these alloys may be utilized in all of its key sectors: water electrolysis, hydrogen storage, and fuel cell applications. Despite the rapid development of MEAs and HEAs with the ability to reversibly absorb hydrogen, the research is limited to transition-metal-based alloys that crystallize in body-centered cubic solid solution or Laves phase structures. To date, no study has been devoted to the hydrogenation of rare-earth-element (REE)-based MEAs or HEAs, as well as to the alloys crystallizing in face-centered-cubic (FCC) or hexagonal-close-packed structures. Here, we elucidate the formation and hydrogen storage properties of REE-based ScYNdGd MEA. More specifically, we present the astounding stabilization of the single-phase FCC structure induced by the hydrogen absorption process. Moreover, the measured unprecedented high storage capacity of 2.5 H/M has been observed after hydrogenation conducted under mild conditions that proceeded without any phase transformation in the material. The studied MEA can be facilely activated, even after a long passivation time. The results of complementary measurements showed that the hydrogen desorption process proceeds in two steps. In the first, hydrogen is released from octahedral interstitial sites at relatively low temperatures. In the second, high-temperature process, it is associated with the desorption of hydrogen atoms stored in tetrahedral sites. The presented results may impact future research of a novel group of REE-based MEAs and HEAs with adaptable hydrogen storage properties and a broad scope of possible applications.
中高熵合金(MEA和HEA)的功能特性研究近来备受关注。最近在与氢基经济相关的研究中取得了许多重大发现,这些合金可用于其所有关键领域:水电解、储氢和燃料电池应用。尽管MEA和HEA在可逆吸收氢方面发展迅速,但研究仅限于在体心立方固溶体或Laves相结构中结晶的过渡金属基合金。迄今为止,尚未有关于稀土元素(REE)基MEA或HEA的氢化研究,以及在面心立方(FCC)或六方密堆积结构中结晶的合金的研究。在此,我们阐明了基于REE的ScYNdGd MEA的形成和储氢特性。更具体地说,我们展示了由氢吸收过程诱导的单相FCC结构的惊人稳定性。此外,在温和条件下氢化后观察到前所未有的2.5 H/M的高储氢容量,且材料未发生任何相变。即使经过长时间的钝化,所研究的MEA仍能轻松活化。补充测量结果表明,氢解吸过程分两步进行。第一步,在相对较低温度下,氢从八面体间隙位置释放。第二步,高温过程中,它与储存在四面体位置的氢原子解吸有关。所呈现的结果可能会影响未来对具有适应性储氢特性和广泛可能应用的新型REE基MEA和HEA的研究。