脱氢
石墨烯
镁
材料科学
镍
纳米颗粒
氮气
无机化学
兴奋剂
化学工程
纳米技术
化学
冶金
催化作用
有机化学
工程类
光电子学
作者
Imran Muhammad,Jaffer Saddique,Chengzhang Wu,Muneeb Ur Rahman,Zaheen Ullah Khan,Wajid Ali,Rong Zhang
出处
期刊:ACS omega
[American Chemical Society]
日期:2024-04-22
卷期号:9 (17): 19261-19271
被引量:12
标识
DOI:10.1021/acsomega.4c00198
摘要
High Resolution Image Download MS PowerPoint Slide Magnesium hydride (MgH 2 ) is a promising hydrogen storage candidate due to its large capacity; however, high dehydrogenation temperature and slow kinetic rates are the main bottlenecks. Herein, we proposed a strategy for designing nitrogen-doped graphene-supported Ni nanoparticles (NPs) (Ni@NC) to tackle these problems. The results showed that the MgH 2 + 15 wt % Ni@NC nanocomposite reduced the on-set dehydrogenation temperature to 195 °C, which was 175 °C lower than pristine MgH 2 . In addition, MgH 2 + 15 wt % Ni@NC achieved 1.7 and 6.5 wt % desorption capacities at 225 and 300 °C, respectively, while absorbing 5.5 wt % hydrogen at 100 °C. The MgH 2 + 15 wt % Ni@NC nanocomposite showed high cyclic stability, achieving 98.0% capacity retention after 100 cycles at 270 °C with negligible loss in capacity. This remarkable hydrogen storage performance can be attributed to the homogeneous distribution of Ni NPs on N-doped graphene layers, in situ formed Mg 2 NiH 2 NPs, and multiphasic regions, promoting the nucleation and growth process during hydrogenation/dehydrogenation, which stabilized and improved the cyclic stability. This strategy paves the way to developing high-performance MgH 2 for large-scale applications.
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