We report a facile approach to directly chlorinate graphene from an aqueous sodium chloride solution under ambient conditions. By applying a moderate anodic voltage to substrate-supported monolayer graphene, the resultant chlorine radicals generated at the graphene surface enable efficient chlorination: X-ray photoelectron spectrum confirms the formation of C-Cl bonds, and reaction voltage-tunable Cl:C atomic ratios of up to 17% are achieved. In comparison, we find the corresponding electrochemical graphene bromination and iodination reactions much less viable. Electrical and Raman characterizations show substantial p-doping for the chlorinated graphene, yet good basal-plane integrity and electrical properties are maintained. Interference reflection microscopy and pH-dependent experiments next help elucidate the competition between the radical-mediated electrochemical chlorination and oxidation in the process, and rationalize acidic conditions for optimal chlorination. Reaction in a mixed NaCl-NaN3 solution shows the electrochemical chlorination to be fully suppressed by azidation, yet a sequential, two-step chlorination-azidation approach permits facile bifunctionalization.
Keyphrases
- drinking water
- ionic liquid
- room temperature
- label free
- gold nanoparticles
- carbon nanotubes
- walled carbon nanotubes
- molecularly imprinted
- quantum dots
- high resolution
- magnetic resonance imaging
- air pollution
- highly efficient
- high intensity
- magnetic resonance
- metal organic framework
- hydrogen peroxide
- high speed
- mass spectrometry
- solid state