Rm. Metzger et al., Electrical rectification by a monolayer of hexadecylquinolinium tricyanoquinodimethanide measured between macroscopic gold electrodes, J PHYS CH B, 105(30), 2001, pp. 7280-7290
Unimolecular rectification was detected between oxide-free Au. electrodes f
or a Langmuir-Blodgett (LB) monolayer of the zwitterionic D+-pi -A(-) molec
ule hexadecylquinolinium tricyanoquinodimethanide, C(16)H(33)Q-3CNQ. The to
p gold pad was deposited by a process that cools the metal vapor before dep
osition. The maximum rectification ratio is 27.5 at 2.2 V (the average rect
ification ratio is 7.55). The currents are as large as 9.04 x 10(4) electro
ns molecule(-1) s(-1). The result reinforces previous work with oxide-beari
ng Al electrodes, but the currents with Au electrodes are larger by 3-5 ord
ers of magnitude. Rectification was also seen for a nine-monolayer Z-type L
B film between similar Au electrodes but not for a monolayer of arachidic a
cid. The direction of enhanced electron current is from the negatively char
ged dicyanomethylene end Of C(16)H(33)Q-3CNQ to the quinolinium ring, as pr
edicted by the Aviram-Ratner analysis. However, there is a good fit to the
behavior expected for quantum conduction dominated by a single molecular le
vel. The best-fit energy for this level is 1.31 +/- 0.25 eV above the Fermi
level of the An electrode.