Rapid and efficient hydrogen clathrate hydrate formation in confined nanospace

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Título: Rapid and efficient hydrogen clathrate hydrate formation in confined nanospace
Autor/es: Farrando Pérez, Judit | Balderas-Xicohtencatl, Rafael | Cheng, Yongqiang | Daemen, Luke L. | Cuadrado-Collados, Carlos | Martinez-Escandell, Manuel | Ramírez-Cuesta, Anibal J. | Silvestre-Albero, Joaquín
Grupo/s de investigación o GITE: Materiales Avanzados
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales
Palabras clave: Hydrogen clathrate | Hydrate formation | Confined nanospace
Fecha de publicación: 10-oct-2022
Editor: Springer Nature
Cita bibliográfica: Nature Communications. 2022, 13:5953. https://doi.org/10.1038/s41467-022-33674-2
Resumen: Clathrate hydrates are crystalline solids characterized by their ability to accommodate large quantities of guest molecules. Although CH4 and CO2 are the traditional guests found in natural systems, incorporating smaller molecules (e.g., H2) is challenging due to the need to apply higher pressures to stabilize the hydrogen-bonded network. Another critical limitation of hydrates is the slow nucleation and growth kinetics. Here, we show that specially designed activated carbon materials can surpass these obstacles by acting as nanoreactors promoting the nucleation and growth of H2 hydrates. The confinement effects in the inner cavities promote the massive growth of hydrogen hydrates at moderate temperatures, using pure water, with extremely fast kinetics and much lower pressures than the bulk system.
Patrocinador/es: We would like to acknowledge financial support from Ministerio de Ciencia e Innovación (Project PID2019-108453GB-C21), MCIN/AEI/10.13039/501100011033 and EU “NextGeneration/PRTR” (Project PCI2020-111968 /3D-Photocat) – JSA. Neutron scattering experiments were performed at ORNL’s Spallation Neutron Source, IPTS-27062, supported by the Scientific User Facilities Division, Office of Basic Energy Sciences, US DOE, under Contract No. DE-AC0500OR22725 with UT Battelle, LLC—J.S.A., Y.Q.C., L.D., A.J.R.C.. We gratefully acknowledge research support from the Hydrogen Materials—Advanced Research Consortium (HyMARC), established as part of the Energy Materials Network under the U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technology Office, under Contract Number DE-AC05-00OR22725—R.B.-X. This manuscript has been authored in part by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The publisher acknowledges the US government license to provide public access under the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).
URI: http://hdl.handle.net/10045/128360
ISSN: 2041-1723
DOI: 10.1038/s41467-022-33674-2
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Revisión científica: si
Versión del editor: https://doi.org/10.1038/s41467-022-33674-2
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