- AFM-IR was used to map oxygen bonding on graphene oxide sheets
- Oxygen bonding was observed most often on the edges of graphene oxide sheets, in areas where graphene is folded, and in discrete domains
- An updated structural model for graphene oxide was proposed, with C=O on its edge and plane
- Determining atomic position and configuration from precise imaging offers the possibility to link nanoscale structure and composition with material function
Z. Liu, K. Nørgaard, M.H. Overgaard, M. Ceccato, D.M.A. Mackenzie, N. Stenger, S.L.S. Stipp, T. Hassenkam
Graphene oxide (GO) is an interesting material that has the potential for a wide range of applications. Critical for these applications are the type of oxygen bond and its spatial distribution on the individual GO sheets. This distribution is not yet well understood. Few techniques offer a resolution high enough to unambiguously identify oxygen conﬁguration.
We used a new, label free spectroscopic technique to map oxygen bonding on GO, with spatial resolution of nanometres and high chemical speciﬁcity. AFM-IR, atomic force microscopy coupled with infrared spectroscopy, overcomes conventional IR diffraction limits, producing IR spectra from speciﬁc points as well as chemical maps that are coupled to topography.
We have directly observed oxygen bonding preferentially on areas where graphene is folded, in discrete domains and on edges of GO. From these observations, we propose an updated structural model for GO, with C=O on its edge and plane, which conﬁrms parts of earlier proposed models.
The results have interesting implications. Determining atomic position and conﬁguration from precise imaging offers the possibility to link nanoscale structure and composition with material function, paving the way for targeted tethering of ions, polymers and biomaterials.
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