Facile fabrication of Mxene-supported nano high-entropy hydride unlocking reversible hydrogen storage in Mg(BH4)2

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ao Xia, Jiaguang Zheng, Zhenxuan Ma, Changhai Wu, Cong Li, Beibei Xiao
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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.
mxene负载的纳米高熵氢化物的制备解锁了Mg(BH4)2中的可逆储氢
采用改进的机械化学方法合成了纳米级高熵氢化物(HEH),并将其均匀负载在Ti3C2上,进一步证明了HEH是提高Mg(BH4)2脱氢动力学和可逆性的有效催化剂。氢在83.5℃时从Mg(BH4)2+30HEH@Ti3C2中解吸,在330℃时氢完全释放量为9.84 wt%。脱氢活化能显著降低至131 kJ/mol和163 kJ/mol,这是脱氢动力学增强的主要原因。循环试验表明HEH@Ti3C2显著增强了Mg(BH4)2的可逆性,第十次试验后可逆性保持在4.6 wt%。本研究通过设计和制造多组分催化剂,为开发高性能催化剂提供了一条新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
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.
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