Published January 1, 2018
| Version v1
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Controlling the charge transfer flow at the graphene/pyrene-nitrilotriacetic acid interface
Creators
- 1. Univ Warsaw, Ctr New Technol, Chem & Biol Syst Simulat Lab, Banacha 2C, PL-02097 Warsaw, Poland
- 2. Univ Warsaw, Ctr New Technol, Solar Fuels Lab, Banacha 2C, PL-02097 Warsaw, Poland
- 3. Mersin Univ, Adv Technol Res & Applicat Ctr, Ciftlikkoy Campus, TR-33343 Yenisehir, Mersin, Turkey
- 4. Pamukkale Univ, Dept Biomed Engn, TR-20070 Denizli, Turkey
Description
The fabrication of highly efficient bio-organic nanoelectronic devices is still a challenge due to the difficulty in interfacing the biomolecular component to the organic counterparts. One of the ways to overcome this bottleneck is to add a self-assembled monolayer (SAM) in between the electrode and the biological material. The addition of a pyrene-nitrilotriacetic acid layer to a graphene metal electrode enhances the charge transfer within the device. Our theoretical calculations and electrochemical results show that the formation of a pyrene-nitrilotriacetic acid SAM enforces a direct electron transfer from graphene to the SAM, while the addition of the Ni2+ cation and imidazole reverses the charge transfer direction, allowing an atomic control of the electron flow, which is essential for a true working device.
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