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Molecular force transfer mechanisms in graphene oxide paper evaluated using atomic force microscopy and in situ synchrotron micro FT-IR spectroscopy

DOI: 10.1039/C4NR03646H DOI Help

Authors: Congwei Wang (Department of Materials, School of Engineering and Materials Science, Queen Mary University of London) , Mark Frogley (Diamond Light Source) , Gianfelice Cinque (Diamond Light Source) , Lu-qi Liu (National Center for Nanoscience and Technology) , Asa Barber (Department of Materials, School of Engineering and Materials Science, Queen Mary University of London)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Nanoscale , VOL 6 (23) , PAGES 14404 - 14411

State: Published (Approved)
Published: October 2014
Diamond Proposal Number(s): 8386

Abstract: The mechanical properties of graphene oxide (GO) paper are critically defined both by the mechanical properties of the constituent GO sheets and the interaction between these sheets. Functional carbonyl and carboxyl groups decorating defects, expected to be predominantly sheet edges of the GO, are shown to transfer forces to the in-plane carbon¬Ėcarbon bonding using a novel technique combining atomic force microscopy (AFM) to mechanically deform discrete volumes of GO materials while synchrotron Fourier-transform infra-red (FTIR) microspectroscopy evaluated molecular level bond deformation mechanisms of the GO. Spectroscopic absorption peaks corresponding to in-plane aromatic C[double bond, length as m-dash]C bonds from GO sheets were observed to shift during tensile tests. Importantly, FTIR provided information on clear absorption peak shifts from C[double bond, length as m-dash]O bonds linking along the GO sheet edges, indicating transfer of forces between both C[double bond, length as m-dash]C and C[double bond, length as m-dash]O bonds during tensile deformation. Gr√ľneisen parameters were used to quantitatively link the macroscopic FTIR peak shifts to molecular level chemical bond strains, with relatively low bond strains prevalent when applying external forces to the GO paper suggesting probing of hydrogen bonding interactions. We propose a mechanistic description of molecular interactions between GO sheets in the paper from these experiments, which is important in future strategies for further modification and improvement of GO-based materials.

Subject Areas: Materials, Chemistry


Instruments: B22-Multimode InfraRed imaging And Microspectroscopy

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