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J Naciri

Publications and source records attributed to J Naciri.

6 recordsLinked to original sources

Fermi level alignment in self-assembled molecular layers: the effect of coupling chemistry.

Photoelectron spectroscopy was used to explore changes in Fermi level alignment, within the pi-pi* gap, arising from modifications to the coupling chemistry of conjugated phenylene ethynylene oligomers to the Au surface. Self-assembled monolayers were formed employing either thiol (4,4'-ethynylphenyl-1-benzenethiol or OPE-T) or isocyanide (4,4'-ethynylphenyl-1-benzeneisocyanide or OPE-NC) coupling. The electronic density of states in the valence region of the two systems are nearly identical with the exception of a shift to higher binding energy by about 0.5 eV for OPE-NC. Corresponding shifts appear in C(1s) spectra and in the threshold near E(F). The lack of change in the optical absorption suggests that a rigid shift of the Fermi level within the pi-pi* gap is the major effect of modifying the coupling chemistry. Qualitative consideration of bonding in each case is used to suggest the influence of chemisorption-induced charge transfer as a potential explanation. Connections to other theoretical and experimental work on the effects of varying coupling chemistries are also discussed.

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Evidence for de Vries structure in a smectic-A liquid crystal observed by polarized Raman scattering.

The second- and fourth-order apparent orientational order parameters of the core part of the molecule P2 (app) and P4 (app) , have been measured by polarized vibrational Raman spectroscopy for a homogeneously aligned ferroelectric smectic liquid crystal with three dimethyl siloxane groups in the achiral terminal chain, which shows de Vries-type phenomena, i.e., very large electroclinic effect in the smectic- A (Sm-A) phase and a negligible layer contraction at the phase transition between the Sm-A and Sm- C(*) phases. The apparent orientational order parameters of the rigid core part of the molecule are extremely small both with and without the external electric field in Sm-A . These results provide evidence for the existence of the de Vries Sm-A phase, where the local molecular director is tilted at a large angle.

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Understanding charge transport in molecular electronics.

For molecular electronics to become a viable technology the factors that control charge transport across a metal-molecule-metal junction need to be elucidated. We use an experimentally simple crossed-wire tunnel junction to interrogate how factors such as metal-molecule coupling, molecular structure, and the choice of metal electrode influence the current-voltage characteristics of a molecular junction.

Computer Simulation↗

Metal-molecule contacts and charge transport across monomolecular layers: measurement and theory.

Charge transport studies across molecular length scales under symmetric and asymmetric metal-molecule contact conditions using a simple crossed-wire tunnel junction technique are presented. It is demonstrated that oligo(phenylene ethynylene), a conjugated organic molecule, acts like a molecular wire under symmetric contact conditions, but exhibits characteristics of a molecular diode when the connections are asymmetric. To understand this behavior, we have calculated current-voltage (I-V) characteristics using extended Huckel theory coupled with a Green's function approach. The experimentally observed I-V characteristics are in excellent qualitative agreement with the theory.

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Anomalous softening of order parameter fluctuations at the smectic-A to -C* transition in a siloxane-substituted chiral liquid crystal.

Unconventional softening of order-parameter fluctuations is observed at the smectic-A to smectic-C* phase transition in a chiral liquid crystal possessing multiple siloxane substituents on its hydrocarbon chains. Together with an optical "stripe" texture detected above the transition, the atypical dynamics can be explained by the pretransitional development within the smectic layers of a modulated state of the order parameter. Conventional soft-mode behavior is restored when the degree of chain substitution is reduced.

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Electroclinic liquid crystals with large induced tilt angle and small layer contraction

Optical and x-ray scattering studies of a chiral, organosiloxane smectic-A liquid crystal indicate a large field induced optical tilt of up to 31 degrees accompanied by a very small contraction of the smectic layers. This result suggests that the molecules have a nonzero tilt even with no applied field, and that the primary effect of the field is to induce long range order in the direction of the molecular tilt.

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