Catalysis derived from three-dimensionally ordered macroporous Nb2O5 towards the hydrogen storage performance of magnesium hydride

被引:17
作者
Chen, Yan [1 ,2 ]
Shao, Yuting [1 ,2 ]
Liu, Yana [1 ,2 ]
Gao, Haiguang [3 ]
Tang, Qinke [1 ,2 ]
Zhu, Yunfeng [1 ,2 ]
Zhang, Jiguang [1 ,2 ]
Wang, Jun [1 ,2 ]
Li, Liquan [1 ,2 ]
Hu, Xiaohui [1 ,2 ]
机构
[1] Nanjing Tech Univ, Coll Mat Sci & Engn, 30 South Puzhu Rd, Nanjing 211816, Peoples R China
[2] Nanjing Tech Univ, Jiangsu Collaborat Innovat Ctr Adv Inorgan Funct C, Nanjing 211816, Peoples R China
[3] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen storage; Catalyst; MgH2; SUPPORTED NANO-NI; SORPTION KINETICS; TRANSITION-METAL; MGH2; CARBON; NANOPARTICLES; IMPROVEMENT;
D O I
10.1016/j.fuel.2024.131025
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A three -dimensionally ordered macroporous (3DOM) Nb2O5 was successfully prepared via the colloidal crystal template method, which demonstrates a significant effect in enhancing the hydrogen storage performances of MgH2. 3DOM Nb2O5 presents an overall macroporous structure with a highly ordered overall arrangement and connected layers. As limiting domains influence of 3DOM structure, Nb2O5 nanoparticles ranging in size from 5 to 15 nm are encapsulated with the amorphous carbon layer. The MgH2-5 wt% 3DOM Nb2O5 MM 30 h composite can absorb 6.35 wt% H-2 in 500 s at 175 C-degrees and desorb 6.95 wt% H-2 in 300 s at 300 C-degrees. The unique Nb2O5 3DOM structure can provide more active sites and a larger contact area for the hydrogen ab/desorption of MgH2. The in situ formed NbHx can promote the dissociation and complexation of molecular hydrogen on its surface and induce the hydrogen boundary/interface diffusion along the Mg/MgH2 interface, thus facilitating the hydrogen ab/desorption reaction of MgH2. In addition, the binding energy transfer of Nb2O5 can be observed by XPS and the electron shift at the MgH2/Nb2O5 interface is further confirmed by the theoretical calculations, which can weaken the Mg -H bond and induce MgH2 to become unstable. This finding will provide ideas for the design and preparation of catalysts with special morphologies for Mg -based hydrogen storage materials.
引用
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页数:10
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