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<field name="value">Rozas Azcona, Sara</field>
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<field name="value">Aguilar Cuesta, Nuria</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0002-9339-4330</field>
<field name="value">Marcos Villa, Pedro A.</field>
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<field name="orcid_id">0000-0002-6890-8088</field>
<field name="value">Bol Arreba, Alfredo</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0003-4641-4826</field>
<field name="value">Aparicio Martínez, Santiago</field>
<field name="authority">30</field>
<field name="confidence">600</field>
<field name="orcid_id">0000-0001-9996-2426</field>
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<field name="value">2026-05-26T06:24:44Z</field>
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<field name="value">2026-05-26T06:24:44Z</field>
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<field name="value">2026-01</field>
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<field name="value">2452-2627</field>
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<field name="value">10.1016/j.flatc.2026.100995</field>
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<field name="value">A multiscale computational study was conducted to investigate graphene-supported thin films composed of a&#xd;
natural deep eutectic solvent (NADES) formed by menthol and decanoic acid (MENTH:DA), with a focus on&#xd;
applications in sustainable CO₂ capture. Density functional theory (DFT) and molecular dynamics (MD) simulations were employed to elucidate interfacial structuring, molecular interactions, and gas adsorption behavior.&#xd;
DFT results indicated a strong interaction between decanoic acid and the graphene surface (− 35.88 kJ/mol),&#xd;
characterized by a parallel orientation that maximizes van der Waals interactions. In contrast, menthol displayed&#xd;
weaker adsorption energies (− 5.15 kJ/mol) and a predominantly perpendicular orientation. MD simulations&#xd;
revealed the formation of distinct adsorption layers, with decanoic acid enriched in the first layer and menthol in&#xd;
the second, while the NADES hydrogen-bonding network remained largely intact. CO₂ exhibited preferential&#xd;
adsorption over flue gas components (N₂, H₂O, O₂), with substantial accumulation in both the first and second&#xd;
interfacial layers. Approximately 50% of the CO₂ content from flue gas mixtures was retained within the&#xd;
structured region. Adsorption performance was found to be largely independent of temperature (303− 323K) and&#xd;
NADES film thickness (20–50 Å). These results provide fundamental insight into NADES–graphene interactions&#xd;
and highlight the potential of type V, naturally derived deep eutectic solvents as selective and environmentally&#xd;
benign materials for CO₂ separation technologie</field>
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<field name="value">This work was funded by the European Union (873005-WORLD-H2020-MSCA-RISE-2019). We also acknowledge SCAYLE (Supercomputación Castilla y León, Spain) and COMPUTAEX (Supercomputación Extremadura, Spain) for providing supercomputing facilities. The statements made herein are solely the responsibility of the authors</field>
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<field name="value">eng</field>
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<field name="value">FlatChem. 2026, V. 55, 100995</field>
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<field name="value">CO2 capture</field>
<field name="value">Flue gas</field>
<field name="value">Deep eutectic solvents</field>
<field name="value">Thin films</field>
<field name="value">Graphene</field>
<field name="value">Quantum chemistry</field>
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<field name="value">Molecular layering and CO₂ selectivity in graphene-supported natural deep eutectic solvent films: An in-silico investigation</field>
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<field name="value">FlatChem</field>
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<field name="value">55</field>
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