Electrochemical Grafting of Graphene Nano Platelets with Aryl Diazonium Salts
Zhipeng Qiu1, Jun Yu1, Peng Yan1
1School of Chemistry and Environmental Engineering, Key Laboratory for Green Chemical Process of Ministry of Education, Hubei Key Lab of Novel Reactor & Green Chemical Technology, Wuhan Institute of Technology , Wuhan 430073, China.
Abstract:
To vary interfacial properties, electrochemical grafting of graphene nano platelets (GNP) with 3,5-dichlorophenyl diazonium tetrafluoroborate (aryl-Cl) and 4-nitrobenzene diazonium tetrafluoroborate (aryl-NO2) was realized in a potentiodynamic mode. The covalently bonded aryl layers on GNP were characterized using atomic force microscopy and X-ray photoelectron spectroscopy. Electrochemical conversion of aryl-NO2 into aryl-NH2 was conducted. The voltammetric and impedance behavior of negatively and positively charged redox probes (Fe(CN)63-/4- and Ru(NH3)62+/3+) on three kinds of aryl layers grafted on GNP reveal that their interfacial properties are determined by the charge states of redox probes and reactive terminal groups (-Cl, -NO2, -NH2) in aryl layers. On aryl-Cl and aryl-NH2 garted GNP, selective and sensitive monitoring of positively charged lead ions as well as negatively charged nitrite and sulfite ions was achieved, respectively. Such a grafting procedure is thus a perfect way to design and control interfacial properties of graphene.
More Related Videos
Related Concept Videos
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism


