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Charge Tunneling along Short Oligoglycine Chains
Mostafa Baghbanzadeh1, Carleen M Bowers1, Dmitrij Rappoport1
1Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford St. Cambridge, MA 02138 (USA).
Charge transport through oligoglycine self-assembled monolayers (SAMs) is rapid, comparable to oligophenyls. Superexchange tunneling via amide bonds, supported by DFT, explains this efficient charge transport mechanism.
Area of Science:
- Molecular electronics
- Surface chemistry
- Materials science
Background:
- Self-assembled monolayers (SAMs) are crucial for molecular electronics.
- Understanding charge transport (CT) mechanisms in SAMs is key to device development.
- Oligoglycines offer a unique molecular backbone for studying CT.
Purpose of the Study:
- To investigate charge transport through N-terminal cysteine-anchored oligoglycine SAMs.
- To compare the charge transport rates of oligoglycine SAMs with other molecular systems.
- To elucidate the mechanism governing charge transport in oligoglycine SAMs.
Main Methods:
- Fabrication of Au(TS)/SAM//Ga2O3/EGaIn junctions.
- Measurement of charge transport rates across oligoglycine SAMs.
- Comparison with structurally related SAMs.
- Density functional theory (DFT) calculations.
Main Results:
- Charge transport through oligoglycine SAMs is significantly faster than through n-alkanethiolates.
- Tunneling rates in oligoglycine SAMs are comparable to those in oligophenyl SAMs of similar length.
- DFT calculations support a superexchange mechanism involving amide bonds.
Conclusions:
- Oligoglycine SAMs facilitate rapid charge transport.
- The charge transport mechanism in oligoglycines involves superexchange facilitated by amide bond interactions.
- Oligoglycines represent a promising class of molecules for molecular electronic applications.
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