Monolayer | EPFL Graph Search

A monolayer is a single, closely packed layer of atoms, molecules, or cells. In some cases it is referred to as a self-assembled monolayer. Monolayers of layered crystals like graphene and molybdenum disulfide are generally called 2D materials. Chemistry A Langmuir monolayer or insoluble monolayer is a one-molecule thick layer of an insoluble organic material spread onto an aqueous subphase in a Langmuir-Blodgett trough. Traditional compounds used to prepare Langmuir monolayers are amphiphilic materials that possess a hydrophilic headgroup and a hydrophobic tail. Since the 1980s a large number of other materials have been employed to produce Langmuir monolayers, some of which are semi-amphiphilic, including polymeric, ceramic or metallic nanoparticles and macromolecules such as polymers. Langmuir monolayers are extensively studied for the fabrication of Langmuir-Blodgett film (LB films), which are formed by transferred monolayers on a solid substrate. A Gibbs monolayer o

Couches auto-assemblées comme interfaces des dispositifs électroluminescents organiques

Michel Carrara

Organic light emitting devices (OLED) are among the most promising future technologies for the manufacture of flat and inexpensive displays. Although OLEDs provide already much higher brightness as compared to liquid crystals devices (LCD), they have a major drawback which limits their industrialisation; they are degrading too quickly. Among the factors acting on the performance of OLEDs, interfaces play an important role. The purpose of this work is to develop stable interfaces by using self-assembled monolayers at the device electrodes. Monolayers of para substituted benzoic acids, grown by the traditional method of self-assembly in solution, were characterised by Langmuir isotherms. The experiments showed that the layers are compact, but the binding between the surface and the adsorbed molecule is weak: -5,7 kJ·mole-1 on indium tin oxide (ITO) and -10,6 kJ·mole-1 on aluminium. These molecules allowed to increase the anode surface potential by 0,2 eV and to decrease the one of the cathode by -0,2 eV. Although giving encouraging results, this method has several disadvantages related to the use of a solvent. This is one reason why a new way of growing self-assembled monolayers was developed, the self-assembly from vapour phase. This new grafting method made it possible to increase the surface potential of ITO by 1,4 eV and to decrease the one of aluminium by 0,9 eV using the same molecules as in solution. Another advantage of this technique is the short growing time of the monolayers. Only one minute is necessary to graft the electrode which is considerably shorter than for the traditional technique where 12 hours are necessary. Moreover, it seems that under clean vacuum conditions, the effect on the surface potential depends only on the molecule and not on the surface composition, nor on the initial potential. Finally, this method allowed to discriminate between the different dipole contributions involved in the surface potential modification by the self-assembled monolayers. In a further step, the extended electrode interface consisting of the self-assembled layer covered by an electroactive material was studied. It appears that the organic material partly screens the monolayer dipole moment due to its polarisability. When the initial electrode surface potential of the modified electrode is far apart from the highest occupied or the lowest unoccupied molecular orbitals of the organic material, no charge transfer is expected and the variation in the surface potential comes only from the polarisability of the material. This variation is weaker in the case of a non-polar substituted diamine, α-NPD (the maximum is 0,3 eV) than in the case of the widely used aluminium complex, Alq3, which has a permanent electrical dipole and thus can induce shifts up to 0,7 eV. On the other hand, if the surface potential is close to the energy level of the occupied or unoccupied molecular orbitals, spontaneous charge transfer can occur between the electrode and the organic material. This increases considerably the measured potential variation during the deposition of the electroactive material. With α-NPD, variations of 0,6 eV are observed and in the case of Alq3 shifts are as important as 0,9 eV. Those negative effects can be decreased by the use of an aliphatic chain between the attachment group and the aromatic cycle in the adsorbed molecules. This positive effect is considerable: it can decrease the electrostatic screening of the adsorbed dipole layer by the electroactive material and prevent the charge transfer induced by the image force effect. Finally, homopolar and bipolar devices were studied to investigate the effect of self-assembled monolayers on the device characteristics. In particular, "electron-only" devices were studied using a grafted or a bare aluminium cathode. To study the injection of holes, homopolar and bipolar devices were conceived, having a grafted or a bare ITO anode. The results clearly demonstrate the decrease of the threshold voltage by using suitable self-assembled monolayers. The reasons for this decrease are numerous: improved alignment of the energy levels due to the permanent electrical dipole of the adsorbates, insulating spacer effect due to the aliphatic chains of some of the molecules and improvement of film morphology.

EPFL2002

An Experimental Setup for Heterogeneous Catalysis on Atomically Defined Metal Nanostructures

Jean-Guillaume De Groot

The main objective of this PhD thesis is to link the atomic scale structure to the catalytic properties of self-assembled nanostructures. The growth and characterization of these nanostructures was carried out in an ultra-high vacuum (UHV) chamber initially designed for the study of the kinetics of epitaxial growth of thin films and nanostructures by variable temperature scanning tunneling microscopy. During this PhD thesis, we built a very sensitive and selective gas detector based on a quadrupole mass spectrometer and adapted to the geometry of this UHV system. The proper functioning of the gas detector is confirmed by temperature programmed desorptions of Xe on Ag(100) which demonstrate the very high sensitivity of the device of about

10^{-6}

~monolayer (ML). The zero-order desorption parameters obtained for the first monolayer of Xe adsorbed on Ag(100) are

E_d=0.22-0.23

~eV with a prefactor

\nu_0

between

4\times10^{12}

^{-1}

and

1 \times10^{13}

^{-1}

. An exchange process between Fe adatoms and Ag atoms from the Ag(100) surface is identified by means of temperature programmed desorption of N

_2

. Desorption spectra suggest that the exchange is complete from an annealing temperature of 140~K. Our study of the catalytic activity of metal nanostructures focuses on the ability of passivated Fe clusters to adsorb N

_2

molecules without dissociating them, which is a fundamental step in the bio-inspired heterogeneous catalysis of ammonia. The first system investigated for the growth of Fe clusters is MgO/Ag(100). Diffusion of Fe adatoms deposited on a MgO monolayer is observed from an annealing temperature of 280~K onwards. Fe clusters with an average size of

12.1\pm 0.5

~atoms are obtained on a MgO monolayer by thermal ripening of 0.072~ML of Fe deposited at 40~K. No sign of N

_2

adsorption was observed on these clusters by thermal programmed desorption investigation. The second system chosen for the growth of Fe clusters is graphene/Ir(111) obtained by chemical vapor deposition. The deposition of 0.3 and 0.4 ML of Fe on a graphene/Ir(111) sample at 50~K, followed by annealing at 300~K, generates a superlattice of Fe clusters which matches the periodicity of the moiré formed by graphene/Ir(111). The theoretically expected mean cluster size is 26 atoms for 0.3~ML of Fe, and 35 atoms for 0.4~ML of Fe. The temperature stability of the clusters obtained with 0.4~ML Fe is investigated from 300~K to 600~K. It is established that Smoluchowski ripening takes place as the annealing temperature increases and the superlattice structure has completely disappeared after annealing at 600~K. Temperature programmed desorption of molecularly adsorbed N

_2

at 50~K on a sample with 0.4~ML of Fe deposited on graphene/Ir(111) reveals 3 desorption peaks at 120~K, 92~K, and 60~K. In addition, slow dissociation of nitrogen molecules at 50~K adsorbed on the higher energy adsorption sites is demonstrated.

EPFL2021

Supramolecular architectures of molecularly thin yet robust free-standing layers

Mina Moradi, Patrick Shahgaldian, Henning Paul-Julius Stahlberg

Stable, single-nanometer thin, and free-standing two-dimensional layers with controlled molecular architectures are desired for several applications ranging from (opto-)electronic devices to nanoparticle and single-biomolecule characterization. It is, however, challenging to construct these stable single molecular layers via self-assembly, as the cohesion of those systems is ensured only by in-plane bonds. We herein demonstrate that relatively weak noncovalent bonds of limited directionality such as dipole-dipole (-CN center dot center dot center dot NC-) interactions act in a synergistic fashion to stabilize crystalline monomolecular layers of tetrafunctional calixarenes. The monolayers produced, demonstrated to be freestanding, display a well-defined atomic structure on the single-nanometer scale and are robust under a wide range of conditions including photon and electron radiation. This work opens up new avenues for the fabrication of robust, single-component, and free-standing layers via bottom-up self-assembly.

American Association for the Advancement of Science (AAAS)2019