Observation of feature ripening inversion effect at the percolation threshold for the growth of thin silver films

AbstractThe growth behavior of thin silver films on organic layers is investigated during deposition by means of simultaneous in-situ monitoring of sheet resistance and transmittance. Thermally evaporated films up to 11nm show a distinct percolation behavior with strong resistance drop at the percolation thickness. Additionally, evaporations are divided into a sequence of one nanometer steps. In the deposition breaks, the films exhibit a ripening effect with an inversion at the percolation thickness, by changing from an increasing to decreasing sheet resistance over time. Scanning electron micrographs suggest same ripening mechanisms for islands below the percolation thickness as for holes above

A spray-coating process for highly conductive silver nanowire networks as the transparent top-electrode for small molecule organic photovoltaics

We present a novel top-electrode spray-coating process for the solution-based deposition of silver nanowires (AgNWs) onto vacuum-processed small molecule organic electronic solar cells. The process is compatible with organic light emitting diodes (OLEDs) and organic light emitting thin film transistors (OLETs) as well. By modifying commonly synthesized AgNWs with a perfluorinated methacrylate, we are able to disperse these wires in a highly fluorinated solvent. This solvent does not dissolve most organic materials, enabling a top spray-coating process for sensitive small molecule and polymer-based devices. The optimized preparation of the novel AgNW dispersion and spray-coating at only 30 °C leads to high performance electrodes directly after the deposition, exhibiting a sheet resistance of 10.0 Ω □−1 at 87.4% transparency (80.0% with substrate). By spraying our novel AgNW dispersion in air onto the vacuum-processed organic p-i-n type solar cells, we obtain working solar cells with a power conversion efficiency (PCE) of 1.23%, compared to the air exposed reference devices employing thermally evaporated thin metal layers as the top-electrode

Designing intrinsically photostable low band gap polymers:a smart tool combining EPR spectroscopy and DFT calculations

A rapid and efficient method to identify the weak points of the complex chemical structure of low band gap (LBG) polymers, designed for efficient solar cells, when submitted to light exposure is reported. This tool combines Electron Paramagnetic Resonance (EPR) using the 'spin trapping method' coupled with density functional theory modelling (DFT). First, the nature of the short life-time radicals formed during the early-stages of photo-degradation processes are determined by a spin-trapping technique. Two kinds of short life-time radical (R and R′O) are formed after 'short-duration' illumination in an inert atmosphere and in ambient air, respectively. Second, simulation allows the identification of the chemical structures of these radicals revealing the most probable photochemical process, namely homolytical scission between the Si atom of the conjugated skeleton and its pendent side-chains. Finally, DFT calculations confirm the homolytical cleavage observed by EPR, as well as the presence of a group that is highly susceptible to photooxidative attack. Therefore, the synergetic coupling of a spin trapping method with DFT calculations is shown to be a rapid and efficient method for providing unprecedented information on photochemical mechanisms. This approach will allow the design of LBG polymers without the need to trial the material within actual solar cell devices, an often long and costly screening procedure

Ferrocenes as potential building blocks for molecular electronics self-assembly and tunneling spectroscopy

The fast and continous development of modern information technology has reached extreme dimensions of density and performance. To enhance the properties of classical silicon based semiconductor technologies, new concepts and materials become increasingly important . One promising technology is the use of organic electronics starting from bulk property-based organic light-emmission and cheap, printable electronics on fl exible substrates . Upon further development, organic electronics have the potential to be used in highly ordered organic thin fi lms and new quantum effect based circuits, employing the properties of single molecules . In this thesis self-assembly as a nanoscale integration method and the resulting structural properties of monolayers are studied for alkanethiols and ferrocenylalkanethiols on gold and for carboxylates on copper. The structural properties of these monolayers have been studied with molecular resolution by scanning tunneling microscopy, gaining new insights into molecular self-assembly . Especially mixed systems of alkanethiols and the electroactive ferrocenylalkanethiols have been studied in detail, achieving a better understanding of the layer formation and a thorough characterization of the electronic behaviour of embedded ferrocenylalkanethiols

A new phase of the c(4x2) superstructure of alkanethiols grown by vapour phase deposition on gold

A self-assembled monolayer of dodecanethiol is grown onto (111) oriented gold by vacuum phase deposition and studied by ultrahigh vacuum scanning tunneling microscopy (STM). The films consist of domains that exhibit the c(4 x 2) over-structure of the hexagonal (square root of 3 x square root of 3)R30 of alkanethiols on gold. The domain size is only limited by the terrace size of the underlying gold. By higher resolution scans a new phase of the c(4 x 2) structure consisting of four inequivalent molecules that display different heights in the STM images is discovered

Rectangular (3x23) superlattice of a dodecanethiol self-assembled monolayer on Au(111) observed by ultra-high-vacuum scanning tunneling microscopy

A rectangular (3 x 2 radical3) surface lattice for long-term-annealed dodecanethiol self-assembled monolayers on Au(111) is observed by ultra-high-vacuum scanning tunneling microscopy. The new lattice has the same density and a unit cell of the same size as the well-known c(4 x 2) reconstruction. In contrast, it does not show hexagonal symmetry but rather a sort of thiol pairing, leading to a shift in the binding position of every second molecule. The described structure is believed to be an intermediate phase close to desorption