Ding Xiaoli, Ding Hongfei, Song Yun, Xiang Cuili, Li Yongtao, Zhang Qingan
School of Materials Science and Engineering, Anhui University of Technology, Ma'anshan, China.
School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin, China.
Front Chem. 2020 Jan 28;7:937. doi: 10.3389/fchem.2019.00937. eCollection 2019.
Developing cheap metal nanocatalysts with controllable catalytic activity is one of the critical challenges for improving hydrogen storage in magnesium (Mg). Here, it is shown that the activity of graphene-anchored Co-Ni nanocatalysts can be regulated effectively by tuning their composition and morphology, which results in significantly improved hydrogen storage in Mg. The catalytic activity of supported Co-Ni nanocatalysts is demonstrated to be highly dependent on their morphology and composition. When Ni was partly substituted by Co, the shape of these nanocatalysts was changed from spherical to plate-like, thus corresponding to a decrease in activity. These alterations intrinsically result in enhanced hydrogen storage properties of MgH, i.e., not only does it exhibit a decreased peak desorption temperature but also a positive change in the initial activation for sorption. The results obtained provide a deep understanding of the tuning of catalytic activity via composition and morphology and further provide insights into improving hydrogen storage in Mg-based materials.
开发具有可控催化活性的廉价金属纳米催化剂是改善镁(Mg)储氢性能的关键挑战之一。在此,研究表明,通过调整石墨烯锚定的Co-Ni纳米催化剂的组成和形态,可以有效调节其活性,从而显著改善Mg的储氢性能。负载型Co-Ni纳米催化剂的催化活性被证明高度依赖于其形态和组成。当Ni被Co部分取代时,这些纳米催化剂的形状从球形变为板状,相应地活性降低。这些变化本质上导致了MgH储氢性能的增强,即它不仅表现出降低的脱附峰值温度,而且在吸附的初始活化方面也有积极变化。所得结果为通过组成和形态调节催化活性提供了深入理解,并进一步为改善镁基材料的储氢性能提供了见解。