Fabrication and replication of high efficiency blazed gratings with grayscale electron beam lithography and UV nanoimprint lithography

In a waveguide-type display for augmented reality, the image is injected in the waveguide and extracted in front of the eye appearing superimposed on the real world scene. An elegant and compact way of coupling these images in and out is by using blazed gratings, which can achieve high diffraction efficiencies, thereby reducing stray light and decreasing the required power levels. This study investigates the fabrication of blazed gratings with grayscale electron beam lithography and the subsequent replication of the realized 3D grating structures in a polymer material with ultraviolet nanoimprint lithography. As such, diffractive elements are realized on a waveguide sheet, with very good control over the dimensions and the profile of the printed features. Blazed gratings are designed for green light (λ= 543 nm) and a diffraction angle of 43°. Making use of a PMMA resist and by carefully optimizing the electron-beam parameters, electron dose distributions and development step, blazed gratings with a pitch of 508 nm and a fill factor of 0.66 are achieved. Finally, a master is realized with two blazed gratings, 3 cm apart, which are replicated using ultraviolet nanoimprint lithography onto a waveguide sheet. The in- and outcoupling of an image through these two blazed gratings is shown, appearing sharp and non-distorted in the environment, and a throughput efficiency of 17.4% is confirmed

Exchange Reactions between Alkanethiolates and Alkaneselenols on Au{111}

When alkanethiolate self-assembled monolayers on Au{111} are exchanged with alkaneselenols from solution, replacement of thiolates by selenols is rapid and complete, and is well described by perimeter-dependent island growth kinetics. The monolayer structures change as selenolate coverage increases, from being epitaxial and consistent with the initial thiolate structure to being characteristic of selenolate monolayer structures. At room temperature and at positive sample bias in scanning tunneling microscopy, the selenolate-gold attachment is labile, and molecules exchange positions with neighboring thiolates. The scanning tunneling microscope probe can be used to induce these place-exchange reactions

Combining solvents and surfactants for inkjet printing PEDOT: PSS on P3HT/PCBM in organic solar cells

A commonly used strategy in the fabrication of organic electronics involves the use of orthogonal solvents, i.e. the alternating use of organic solvents and water for the application of consecutive layers to prevent dissolution of previous layers. This strategy therefore requires the deposition of sequential layers with a large mismatch in surface energy. In case of organic photovoltaics (OPV) a particularly challenging deposition is that of the aqueous Poly(3,4-ethylenedioxythiophene) Polystyrene sulfonate (PEDOT:PSS) on the hydrophobic Poly(3-hexylthiophene-2,5-diyl/Phenyl-C61-butyric acid methyl ester (P3HT/PCBM) layer. The mismatch in surface energy causes dewetting and inhomogeneous layer formation. In inkjet printing individually placed droplets should spread sufficiently far to form a homogeneous closed layer before the solvents in the droplet evaporate. A formulation for the aqueous PEDOT:PSS layer has been developed in which the combination of solvents and surfactants is essential for achieving a homogenous layer on the timescales needed for inkjet printing. Homogenous layers of PEDOT:PSS on P3HT/PCBM were achieved for layer thicknesses from 400 nm to 50 nm. The efficiency of the OPV's fabricated with the new formulation were comparable with reference devices, where evaporated molybdenum oxide (MoOx) was used as a topelectrode. This shows that by the addition of solvents and surfactants a hydrophilic solution can be inkjet printed successfully to form homogenous layers on hydrophobic surfaces and achieve good efficiencies in an inverted organic solar cell.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Novel Aerospace Material

Exchange reactions between alkanethiolates and alkaneselenols on Au{111}.

When alkanethiolate self-assembled monolayers on Au{111} are exchanged with alkaneselenols from solution, replacement of thiolates by selenols is rapid and complete, and is well described by perimeter-dependent island growth kinetics. The monolayer structures change as selenolate coverage increases, from being epitaxial and consistent with the initial thiolate structure to being characteristic of selenolate monolayer structures. At room temperature and at positive sample bias in scanning tunneling microscopy, the selenolate-gold attachment is labile, and molecules exchange positions with neighboring thiolates. The scanning tunneling microscope probe can be used to induce these place-exchange reactions

Die Gespräche, taggrau

Il y a du poème. Ça arrive. Comment – la prise de parole du poète ? L’événement aléatoire de la parole dit aussi l’institution fragile du moi, car « nous ne possédons pas notre moi, il nous vient du dehors, porté par le vent », peut-être par ce que Ezra Pound aurait appelé « the eternal moods of the bleak wind » de l’Antiquité. Dire cela à soi-même comme à un autre, se tutoyer et dire finalement sa voix tourbillonnée par un souffle sidéral, par le Strahlenwind du langage : « Au gré du vent qu..

Exchange Reactions between Alkanethiolates and Alkaneselenols on Au{111}

When alkanethiolate self-assembled monolayers on Au{111} are exchanged with alkaneselenols from solution, replacement of thiolates by selenols is rapid and complete, and is well described by perimeter-dependent island growth kinetics. The monolayer structures change as selenolate coverage increases, from being epitaxial and consistent with the initial thiolate structure to being characteristic of selenolate monolayer structures. At room temperature and at positive sample bias in scanning tunneling microscopy, the selenolate–gold attachment is labile, and molecules exchange positions with neighboring thiolates. The scanning tunneling microscope probe can be used to induce these place-exchange reactions