Entanglement of N-doped graphene in resorcinol-formaldehyde: Effect over nanoconfined LiBH4 for hydrogen storage

N-doped graphene hydrogels were prepared by crosslinking graphene oxide with ethylenediamine. These materials presented 10 at. % nitrogen, as determined by X-ray photoelectron spectroscopy. N-doped graphene was entangled within mesoporous matrices by diffusion of resorcinol-formaldehyde solutions th...

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Veröffentlicht in:Carbon (New York) 2019-06, Vol.147, p.284-294
Hauptverfasser: Gasnier, Aurélien, Luguet, Margaux, Pereira, Amaru González, Troiani, Horacio, Zampieri, Guillermo, Gennari, Fabiana C.
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Sprache:eng
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Zusammenfassung:N-doped graphene hydrogels were prepared by crosslinking graphene oxide with ethylenediamine. These materials presented 10 at. % nitrogen, as determined by X-ray photoelectron spectroscopy. N-doped graphene was entangled within mesoporous matrices by diffusion of resorcinol-formaldehyde solutions throughout the hydrogels. According to nitrogen desorption isotherms, N-doping graphene slightly reduces the pore size and volume toward values closer to the graphene-free resins. The underlying graphene framework was observed within the amorphous porous carbon by transmission microscopy. These porous materials were impregnated with LiBH4 at 30, 50 and 70 vol %. Differential scanning calorimetry of the nanoconfined hydrides illustrates how N-doped matrix promotes a decrease in LiBH4 decomposition temperature, and this effect was quantified by volumetric studies. Powder diffraction revealed a peak at 12.6° attributed to the interaction of LiBH4 with the N-doped matrix. Owing to Yates analysis, N-doping lowers hydrogen release temperature by 10 °C, while at 325 °C the quantity released is increased by 1 wt %. This effect is more important than the diminution of pore size from 10 to 5 nm and compensates the presence of graphene. The benefit from N-doping is more remarkable for lower size of pores and higher LiBH4 filling, as illustrated by the proposed model. [Display omitted]
ISSN:0008-6223
1873-3891
DOI:10.1016/j.carbon.2019.02.090