{"title":"Facile fabrication of Mxene-supported nano high-entropy hydride unlocking reversible hydrogen storage in Mg(BH4)2","authors":"Ao Xia, Jiaguang Zheng, Zhenxuan Ma, Changhai Wu, Cong Li, Beibei Xiao","doi":"10.1039/d5cc01503k","DOIUrl":null,"url":null,"abstract":"Nano-sized high-entropy hydrides (HEH) were synthesized and uniformly loaded onto Ti3C2 via a modified mechanochemical method and were further demonstrated as an efficient catalyst for enhancing the hydrogen desorption kinetics and reversibility of Mg(BH4)2. The hydrogen was desorbed from Mg(BH4)2+30HEH@Ti3C2 at 83.5 °C, with a complete hydrogen release of 9.84 wt% achieved at 330 °C. The dehydrogenation activation energies were notably reduced to 131 kJ/mol and 163 kJ/mol, which were identified as the primary factors responsible for the enhanced dehydrogenation kinetics. Cyclic tests revealed that the HEH@Ti3C2 significantly enhanced the reversible ability of Mg(BH4)2, maintaining a reversibility of 4.6 wt% after 10th test. This study introduced a new approach to developing high-performance catalysts through the design and fabrication of multi-component catalysts.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"33 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc01503k","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Nano-sized high-entropy hydrides (HEH) were synthesized and uniformly loaded onto Ti3C2 via a modified mechanochemical method and were further demonstrated as an efficient catalyst for enhancing the hydrogen desorption kinetics and reversibility of Mg(BH4)2. The hydrogen was desorbed from Mg(BH4)2+30HEH@Ti3C2 at 83.5 °C, with a complete hydrogen release of 9.84 wt% achieved at 330 °C. The dehydrogenation activation energies were notably reduced to 131 kJ/mol and 163 kJ/mol, which were identified as the primary factors responsible for the enhanced dehydrogenation kinetics. Cyclic tests revealed that the HEH@Ti3C2 significantly enhanced the reversible ability of Mg(BH4)2, maintaining a reversibility of 4.6 wt% after 10th test. This study introduced a new approach to developing high-performance catalysts through the design and fabrication of multi-component catalysts.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.