Interface-Engineered Charge Transport Properties in Benzenedithol Molecular Electronic Junctions via Chemically p-doped Graphene Electrodes.

In this study, we fabricated and characterized vertical molecular junctions consisting of self-assembled monolayers of benzenedithiol (BDT) with a p-doped multilayer graphene electrode. The p-type doping of a graphene film was performed by treating pristine graphene (work function of ~4.40 eV) with trifluoromethanesulfonic (TFMS) acid, producing a significantly increased work function (~5.23 eV). The p-doped graphene-electrode molecular junctions statistically showed an order of magnitude higher current density and a lower charge injection barrier height than those of the pristine graphene-electrode molecular junctions, as a result of interface engineering. This enhancement is due to the increased work function of the TFMS-treated p-doped graphene electrode in the highest occupied molecular orbital-mediated tunneling molecular junctions. The validity of these results was proven by theoretical analysis based on a coherent transport model that consider asymmetric couplings at the electrode-molecule interfaces.