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<field name="value">Bol Arreba, Alfredo</field>
<field name="authority">70</field>
<field name="confidence">600</field>
<field name="orcid_id">0000-0003-4641-4826</field>
<field name="value">Gómez Ayala, Mª Isabel</field>
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<field name="confidence">600</field>
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<field name="value">Cordero Tejedor, Nicolás A.</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0002-3609-4163</field>
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<field name="value">2023-03-14T13:30:02Z</field>
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<field name="value">2023-03-14T13:30:02Z</field>
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<field name="value">2023-01</field>
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<field name="value">http://hdl.handle.net/10259/7543</field>
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<field name="value">10.3390/micro3010011</field>
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<field name="value">2673-8023</field>
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<field name="value">Using exfoliating agents is one of the most promising ways for large-scale production of&#xd;
liquid dispersed graphenic materials from graphite. Therefore, it is crucial to know the reason why&#xd;
some molecules have a larger exfoliating power than others. The highest reported experimental yield&#xd;
for the liquid phase single-surfactant spontaneous exfoliation of graphite, i.e., without sonication,&#xd;
has been obtained using chlorosulfonic acid. The ability of this acid to disperse graphite is studied&#xd;
within the framework of Density Functional Theory (DFT). Equilibrium configurations, electron&#xd;
transfers, binding energies, and densities of states are presented for two acid concentrations and for&#xd;
two situations: adsorption (on monolayer and bilayer graphene) and intercalation (in between simple&#xd;
hexagonal and Bernal-stacked bilayer graphene). Experimental exfoliation power and dispersion&#xd;
stability are explained in terms of charge transfer—the largest found among several studied exfoliating&#xd;
and surfactant agents—facilitated by the good geometrical matching of chlorosulfonic acid molecules&#xd;
to constituent carbon rings of graphene. This matching is in the origin of the tendency toward&#xd;
adsorption of chlorosulfonic acid molecules on graphene monolayers when they separate, originating&#xd;
the charging of the monolayers that precludes their reaggregation.</field>
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<field name="value">This work was supported by the Spanish MICINN and the European Regional Development Fund (grant MAT2014-54378-R) as well as Junta de Castilla y León (grant VA050U14).</field>
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<field name="value">eng</field>
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<field name="value">MDPI</field>
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<field name="value">Micro. 2023, V. 3, n. 1, p. 143-155</field>
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<field name="value">https://doi.org/10.3390/micro3010011</field>
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<field name="value">info:eu-repo/grantAgreement/MINECO//MAT2014-54378-R/ES/SINERGIAS ENTRE CARBONES POROSOS Y NANOPARTICULAS: APLICACIONES AL ALMACENAMIENTO Y USO DE HIDROGENO COMO COMBUSTIBLE Y A CATALISIS/</field>
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<field name="value">Atribución 4.0 Internacional</field>
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<field name="value">Graphene</field>
<field name="value">Exfoliation</field>
<field name="value">Chlorosulfonic acid</field>
<field name="value">DFT</field>
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<field name="value">Física</field>
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<field name="value">Graphene Formation through Spontaneous Exfoliation of Graphite by Chlorosulfonic Acid: A DFT Study</field>
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<field name="value">Micro</field>
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