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Speaker-Michal Otyepka

Michal Otyepka
Palacký University Olomouc
Full Professor and Head of Department of Physical Chemistry at Palacký University Olomouc and Vice-Director of Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacký University Olomouc. His main scientific activities focus on interdisciplinary research in computer simulations of complex molecular structures and processes, physical chemistry, surface properties and nanomaterials. He contributed to discovery of fluorographene and fluorographene reactivity leading to new graphene derivatives. He studies chemistry in two-dimensions under support of ERC Consolidator grant awarded 2016. He authored and coauthored more than 150 peer-reviewed scientific papers in major journal.
Title:Synthesis of Graphene Derivatives from Fluorographene
SymposiumB6 Sensors
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Abstract

Graphene covalent derivatization represents a vivid approach to module its properties, e.g., electronic structure, water dispersability etc., and enhances its application potential. However, a direct derivatization of graphene is impractical due to its low reactivity. Fluorographene is a stoichiometric and well-defined graphene derivative. Being perfluorinated hydrocarbon, fluorographene was considered unreactive. A few examples document that fluorographene can be converted to graphene derivatives at rather mild conditions. For instance, theas prepared thiofluorographene exhibits suitable electrochemical sensing properties.     
Covalent functionalization of graphene significantly modulates its physical chemical properties and broadens its application potential.1,2In 2010,the stoichiometric derivative of graphene named fluorographene was prepared.3-5 Fluorographene electronic properties considerably differ from graphene, because it has a wide band-gap (~8 eV)6-8 and is considered the thinnest insulator.4It can be prepared by fluorination of graphene, mechanical or chemical exfoliation of graphite fluoride, which is industrially used lubricant. The preparation of flurographene dispersions can be easily up-scaled, e.g., following the procedures suggested for graphene by Coleman and coworkers.9Flurographene (CF)nis a perfluorinated hydrocarbon and therefore it was considered unreactive.4 It is also thermally stable material up to 300 °C.4 The low reactivity of fluorographene was questioned by early experiments, which shown that at higher temperature (180 °C) it could react with KI and produced low quality graphene.5This reaction was, however, considered a curiosity. Very recently it was shown that fluorographene reacted at very mild conditions as electrophile with many nucleophiles.10-13Namely the reaction with NaSHleading to preparation of thiofluorographeneshould be highlighted, because thiofluorographene can be effectively used for electrochemical sensing applications.13 These results indicate that fluorographene is a very promising material for large-scale preparation of dispersions of various graphene derivatives with designed properties. Further prospects and very recent advances in fluorographene derivations will also be discussed.
Acknowledgement: Support from grants ERC (683024) by EU; LO1305 by MEYS of CZ and Neuron fund are gratefully acknowledged.

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Abstract: Minyang Lu

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