4.8 Article

Is Graphene a Stable Platform for Photocatalysis? Mineralization of Reduced Graphene Oxide With UV-Irradiated TiO2 Nanoparticles

Journal

CHEMISTRY OF MATERIALS
Volume 26, Issue 15, Pages 4662-4668

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cm5026552

Keywords

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Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U. S. Department of Energy [DE-FC02-04ER15533]
  2. Bayer Environmental Research Fellowship
  3. University of Notre Dame under ND Nano undergraduate fellowship program
  4. University of Notre Dame under iSURE undergraduate fellowship program
  5. NSF - University of Wisconsin Materials Research Science and Engineering Center [DMR-1121288]

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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 TiO2 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 TiO2 in aqueous media and establish its reactivity toward OH radicals, a primary oxidant generated at the TiO2 surface. By probing changes in absorption, morphology, and total organic carbon content (TOC), we conclusively demonstrate the vulnerability of RGO toward OH center dot attack and raise the concern of its use in many applications where OH center dot are likely to be formed. On the other hand, the OH center dot 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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