石墨烯支持的MgNi合金纳米复合材料作为室温储氢材料-实验和理论见解

S. S. Samantaray, P. Anees, Vinayan Bhaghavathi Parambath, R. S.
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引用次数: 19

摘要

采用密度泛函理论(DFT)对石墨烯负载MgNi合金纳米复合材料的储氢性能进行了实验研究。本研究的主要亮点是纳米结构和Ni与Mg的合金化及其在石墨烯(MgNi/G)和氮/硼掺杂石墨烯(MgNi/NG, MgNi/BG)上的分散导致储氢能力的显著增强。MgNi/G、MgNi/BG和MgNi/NG在室温和3mpa压力下的储氢量分别为~ 2.5 wt. %、3.5 wt. %和5.4 wt. %。值得注意的是,在相同的实验条件下,与报告的G (0.5 wt. %)、BG (0.7 wt. %)和NG (0.9 wt. %)相比,储氢容量有了很大的提高。DFT计算揭示了这种增强的吸氢能力的吸附机制,并证实了实验结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graphene Supported MgNi Alloy Nanocomposite as a Room Temperature Hydrogen Storage Material – Experiments and Theoretical Insights
Abstract Experimental studies along with density functional theory (DFT) calculations have been performed to probe and understand the hydrogen storage properties of graphene supported MgNi alloy nanoparticles nanocomposites. The main highlight of the present work is that nanostructuring and alloying of Mg with Ni and its dispersion on graphene (MgNi/G) & nitrogen/boron doped graphene (MgNi/NG, MgNi/BG) resulted in a substantial enhancement in the hydrogen storage capacity. The hydrogen storage capacity measured at room temperature and at 3 MPa pressure for MgNi/G, MgNi/BG and MgNi/NG are ∼2.5 wt. %, 3.5 wt. % and 5.4 wt. % respectively. The large improvement in hydrogen storage capacity compared to the reported values of G (0.5 wt. %), BG (0.7 wt. %) and NG (0.9 wt. %) under the same experimental conditions is noteworthy. DFT calculations shed light on the adsorption mechanism underlying this enhanced hydrogen uptake capacity and corroborate the experimental results.
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