The recent thrust in utilizing reduced graphene oxide (RGO) as a support for nanostructured catalyst particles has led to the claims of improved efficiency in solar cells, fuel cells, and photocatalytic degradation of pollutants. Specifically, the robust TiO 2 system is often coupled with RGO to improve charge separation and facilitate redox reactions. Here, we probe the stability of RGO in the presence of UV-excited TiO 2 in aqueous media and establish its reactivity toward OH • radicals, a primary oxidant generated at the TiO 2 surface. By probing changes in absorption, morphology, and total organic carbon content (TOC), we conclusively demonstrate the vulnerability of RGO toward OH • attack and raise the concern of its use in many applications where OH • are likely to be formed. On the other hand, the OH • radical-mediated mineralization could also enable new approaches in tackling environmental remediation of nanocarbons such as RGO, carbon nanotubes, and fullerenes.
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Radich et al. (2014) studied this question.
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