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Reactivity of fluorographene is triggered by point defects: beyond the perfect 2D world

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F18%3A73591353" target="_blank" >RIV/61989592:15310/18:73591353 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlepdf/2018/nr/c7nr09426d" target="_blank" >https://pubs.rsc.org/en/content/articlepdf/2018/nr/c7nr09426d</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c7nr09426d" target="_blank" >10.1039/c7nr09426d</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Reactivity of fluorographene is triggered by point defects: beyond the perfect 2D world

  • Original language description

    Preparation of graphene derivatives using fluorographene (FG) as a precursor has become a key strategy for the large-scale synthesis of new 2-D materials (e.g. graphene acid, cyanographene, allyl-graphene) with tailored physicochemical properties. However, to gain full control over the derivatization process, it is essential to understand the reaction mechanisms and accompanying processes that affect the composition and structure of the final products. Despite the strength of C-F bonds and high chemical stability of perfluorinated hydrocarbons, FG is surprisingly susceptible to reactions under ambient conditions. There is clear evidence that nucleophilic substitution on FG is accompanied by spontaneous defluorination, and solvent-induced defluorination can occur even in the absence of any nucleophilic agent. Here, we show that distributed radical centers (fluorine vacancies) on the FG surface need to be taken into account in order to rationalize the defluorination mechanism. Depending on the environment, these radical centers can react as electron acceptors, electrophilic sites and/or cause homolytic bond cleavages. We also propose a new radical mechanism of FG defluorination in the presence of N,N&apos;-dimethylformamide (DMF) solvent. Spin-trap experiments as well as F-19 NMR measurements unambiguously confirmed formation of N,N&apos;-dimethylformyl radicals and also showed that N,N&apos;-dimethylcarbamoyl fluoride plays a key role in the proposed mechanism. These findings imply that point defects in 2D materials should be considered as key factor determining their chemical properties and reactivity.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Nanoscale

  • ISSN

    2040-3364

  • e-ISSN

  • Volume of the periodical

    10

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    4696-4707

  • UT code for WoS article

    000428786800010

  • EID of the result in the Scopus database

    2-s2.0-85043500437