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通过添加花状 NiS 形成用于 Mg 纳米颗粒储氢的多相催化剂。

Formation of Multiple-Phase Catalysts for the Hydrogen Storage of Mg Nanoparticles by Adding Flowerlike NiS.

机构信息

Key Laboratory of Aerospace Materials and Performance (Ministry of Education), School of Materials Science and Engineering, Beihang University , No.37 Xueyuan Road, Beijing, 100191, China.

Beijing National Laboratory for Molecular Sciences (BNLMS), The State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, China.

出版信息

ACS Appl Mater Interfaces. 2017 Feb 22;9(7):5937-5946. doi: 10.1021/acsami.6b13222. Epub 2017 Feb 8.

DOI:10.1021/acsami.6b13222
PMID:28121127
Abstract

In order to enhance the hydrogen storage properties of Mg, flowerlike NiS particles have been successfully prepared by solvothermal reaction method, and are subsequently ball milled with Mg nanoparticles (NPs) to fabricate Mg-5 wt % NiS nanocomposite. The nanocomposite displays Mg/NiS core/shell structure. The NiS shell decomposes into Ni, MgS and MgNi multiple-phases, decorating on the surface of the Mg NPs after the first hydrogen absorption and desorption cycle at 673 K. The Mg-MgS-MgNi-Ni nanocomposite shows enhanced hydrogenation and dehydrogenation rates: it can quickly uptake 3.5 wt % H within 10 min at 423 K and release 3.1 wt % H within 10 min at 573 K. The apparent hydrogen absorption and desorption activation energies are decreased to 45.45 and 64.71 kJ mol. The enhanced sorption kinetics of the nanocomposite is attributed to the synergistic catalytic effects of the in situ formed MgS, Ni and MgNi multiple-phase catalysts during the hydrogenation/dehydrogenation process, the porthole effects for the volume expansion and microstrain of the phase transformation of MgNi and MgNiH and the reduced hydrogen diffusion distance caused by nanosized Mg. This novel method of in situ producing multiple-phase catalysts gives a new horizon for designing high performance hydrogen storage material.

摘要

为了提高镁的储氢性能,通过溶剂热反应方法成功制备了花状 NiS 颗粒,然后与 Mg 纳米颗粒(NPs)球磨,制备 Mg-5wt%NiS 纳米复合材料。该纳米复合材料显示出 Mg/NiS 核/壳结构。NiS 壳在 673K 的第一次吸氢和脱氢循环后分解为 Ni、MgS 和 MgNi 多相,装饰在 Mg NPs 的表面。Mg-MgS-MgNi-Ni 纳米复合材料表现出增强的加氢和脱氢速率:它可以在 423K 下 10 分钟内快速吸收 3.5wt%H,并在 573K 下 10 分钟内释放 3.1wt%H。表观氢吸收和解吸活化能降低至 45.45 和 64.71kJ/mol。纳米复合材料的增强吸附动力学归因于在加氢/脱氢过程中原位形成的 MgS、Ni 和 MgNi 多相催化剂的协同催化作用、MgNi 和 MgNiH 相变的体积膨胀和微应变的孔眼效应以及纳米尺寸 Mg 引起的氢扩散距离缩短。这种原位生成多相催化剂的新方法为设计高性能储氢材料提供了新的前景。

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