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dc.contributor.authorRodríguez Padrón, Daily
dc.contributor.authorPuente-Santiago, Alain R.
dc.contributor.authorCano, Manuel
dc.contributor.authorCaballero, Álvaro
dc.contributor.authorMuñoz Batista, Mario Jesús 
dc.contributor.authorLuque, Rafael
dc.date.accessioned2024-01-22T13:27:43Z
dc.date.available2024-01-22T13:27:43Z
dc.date.issued2019-12
dc.identifier.citationPublished version: https://doi.org/10.1021/acsami.9b13571es_ES
dc.identifier.urihttps://hdl.handle.net/10481/87100
dc.description.abstractA graphitic carbon nitride nanostructure has been successfully functionalized by incorporation of different silver contents and subsequent modification with an α-rich protein, namely hemoglobin. Mechanochemistry has been employed, as an efficient and sustainable procedure, for the incorporation of the protein. A complete characterization analysis has been performed following a multitechnique approach. Particularly, XPS data exhibited considerable differences in the C 1s region for the Hb/xAg@CN, ensuring the successful protein anchorage on the surface of the graphitic carbon nitride-based materials. The as-synthesized nanomaterials delivered impressive performance toward hydrogen evolution reactions with an overpotential of 79 mV at a current density of 10 mA/cm2 for Hb/20Ag@CN nanohybrids, which is comparable with the most efficient HER electrocatalysts reported in the literature. The outstanding HER properties were associated with the unique synergistic interactions, quantitatively measured, between AgNPs, Hb tertiary architecture, and the graphitic carbon nitride networks.es_ES
dc.language.isoenges_ES
dc.titleImproving electrochemical hydrogen evolution of Ag@CN nanocomposites by synergistic effects with α-rich proteinses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/acsami.9b13571


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