2021
DOI: 10.1016/j.jallcom.2020.158004
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Enhancing hydrogen storage properties of MgH2 by core-shell CoNi@C

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Cited by 40 publications
(12 citation statements)
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“…Many forms of carbonaceous matrix have been employed: C-replica of mesoporous silica, C-NTs, C-foam, C-spheres, graphene, graphene oxide GO, reduced graphene oxide r-GO etc. (Table 2) [40,42,53,65,69,70,.…”
Section: Types Of Hosts Used As Hydride Matrixmentioning
confidence: 99%
See 1 more Smart Citation
“…Many forms of carbonaceous matrix have been employed: C-replica of mesoporous silica, C-NTs, C-foam, C-spheres, graphene, graphene oxide GO, reduced graphene oxide r-GO etc. (Table 2) [40,42,53,65,69,70,.…”
Section: Types Of Hosts Used As Hydride Matrixmentioning
confidence: 99%
“…The overall enhancement of kinetic and thermodynamic parameters can be tuned by utilization of catalysts. This is usually implemented to improve behavior of systems that already show promising results including recyclability (Table 9) [19,20,34,43,57,65,68,77,82,92,102,108,113,118,120,125,131,132,134,136,139,143,147,158,160,[166][167][168]172,[183][184][185][186][187][188][189][190][191][192]194,[196][197][198][199][200][201][202][203]…”
Section: (Nano)catalyst Additionmentioning
confidence: 99%
“…The catalytic mechanism was well explained in ref [116]; accordingly, the Mg 2 NiH 4 phase decomposes earlier than MgH 2 during the desorption process; the newly created Mg 2 Ni can assist the dehydrogenation of MgH 2 in a way that H atoms first diffuse to the Mg 2 Ni and then to the solid-gas interface. This mechanism is often referred to as a "hydrogen pump" [44,117,118], since the intermetallic phase acts as a diffusion channel for hydrogen and also serves as a heterogeneous nucleation site. It was also pointed out that the micro-strain associated with the volume change occurring during the Mg 2 Ni↔Mg 2 NiH 4 transformation is beneficial for the diffusion of H and, thus, the kinetic performance of the composite [110,119].…”
Section: Formation Of Catalysts During In Situ Reactionsmentioning
confidence: 99%
“…In terms of catalytic activity, they often surpass those additives that are not formed in situ, but only mixed with MgH 2 through ball milling. The reason behind this observation can have multiple origins: (i) the in situ formed phases have altered the electronic structure compared to the original additive [41,102,109,128], which could be beneficial to the interaction with hydrogen atoms/molecules; (ii) the small size and uniform distribution (which were observed in multiple cases [41,109,110,117,128]) are also an important feature for in situ generated catalysts, since more interphase regions and a larger surface area covered by these products lead to an enhanced overall catalytic activity.…”
Section: Formation Of Catalysts During In Situ Reactionsmentioning
confidence: 99%
“…After dehydrogenation, 0.6 wt% H 2 was absorbed under 300 bar pressure at 300 • C temperature in 11 h by the dehydrogenated product. Zhao et al designed a catalyst containing core-shell structure CoNi@C via hydrothermal and calcination reduction to improve the catalytic activity of MgH 2 [159]. Prepared catalyst was found to efficiently desorb 5.83 wt% hydrogen within 1800 s started at 173 • C up to max 275 • C temperature and released 4.83 wt% H 2 within 1800 s at the lowest temperature 100 • C. Meng et al investigated the superiority of designed 3D flower-like TiO 2 @C nanostructured catalyst towards MgH 2 [160].…”
Section: D-block Ternary Metal Catalysts and Miscellaneous Catalystsmentioning
confidence: 99%