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Updated: Apr 25, 2026

Scalable Syntheses of Graphene Oxide and Reduced Graphene Oxide using Cascade Design Oxidation and Highly Basic Reduction Reactions
Published on: July 3, 2025
Transformation and destabilization of graphene oxide in reducing aqueous solutions containing sulfide
Heyun Fu1, Xiaolei Qu, Wei Chen
1State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Jiangsu, China.
Abstract:
The colloidal stability of carbon nanomaterials is a key factor controlling their fate and bioavailability in natural aquatic systems. The authors report that graphene oxide nanoparticles could be destabilized in reducing aqueous solutions containing a low concentration (0.5 mM) of sulfide, a naturally occurring reductant. Spectroscopic characterization using combined X-ray photoelectron, Fourier-transform infrared, X-ray diffraction, and Raman analyses revealed that the surface oxygen-containing groups (mainly epoxy groups) of graphene oxide were significantly reduced after reacting with sodium sulfide. The destabilization of graphene oxide was likely caused by the enhanced surface hydrophobicity of the reduced graphene oxide, whereas electrostatic repulsion played a minimal role. Solution pH was found to affect both the deoxygenation process and the aggregation behavior of graphene oxide. Coexisting humic acid reduced the reaction efficiency and stabilized graphene oxide through steric hindrance. These findings suggest for the first time that the colloidal behavior of carbon nanomaterials might change drastically when they enter natural reducing environments containing sulfide such as anaerobic aquifers and sediments.
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