The microstructure of blend films of conjugated polymer and fullerene, especially the degree of mixing and crystallization, impacts the performance of organic photovoltaic devices considerably. Mixing and crystallization affect device performance in different ways. These phenomena are not easy to screen using traditional methods such as imaging. In this paper, the amorphous regiorandom poly(3‐hexylthiophene) is blended with the potentially crystalline fullerene [6,6]‐phenyl‐C 61 ‐butyric acid methyl ester PCBM and the amorphous bis‐adduct. First, the degree of mixing of polymer: fullerene blends is evaluated using UV–Vis absorption, steady‐state and ultra‐fast photoluminescence spectroscopy. The blue‐shift of the polymer emission and absorption onset are used in combination with the saturation of the polymer emission decay time upon fullerene addition in order to infer the onset of aggregation of the blends. Second, the crystallinity of the fullerene is probed using variable angle spectroscopic ellipsometry (VASE), electroluminescence and photoluminescence spectroscopy. It is shown that the red‐shift of charge transfer emission in the case of PCBM based blends cannot be explained solely by a variation of optical dielectric constant as probed by VASE. A combination of optical spectroscopy techniques, therefore, allows to probe the degree of mixing and can also distinguish between aggregation and crystallization of fullerenes.

We address the impact of the relative orientation between donor (D) and acceptor (A) molecules at the D/A heterojunction on the exciton dissociation. For this purpose, two-dimensional heterojunctions of diindenoperylene (DIP) and N,N'-dioctyl-3,4,9,10-perylene tetracarboxylicdiimide (PTCDI-C-8) deposited onto SiO2/Si are grown, which exemplify two model interfaces with the pi-staking direction either perpendicular or parallel to the interface. Aspects related to the morphology of the heterojunctions and charge photogeneration are studied by scanning probe force methods and photoluminescence (PL) spectroscopy. Results from PL spectroscopy indicate that the exciton dissociation is influenced by the different relative molecular orientations of A and D. For the configuration with stronger orbital overlap between A and D at the interface, the exciton dissociation is dominated by recombination from an interfacial charge-transfer state.

We have developed organic photodetectors based on two complementary wedge layers made of CuPc and C60 and observed a strong spatial dependence of the spectral response on the position of the incident light spot. Photocurrent measurements are correlated with atomic force microscopy (AFM), micro-Raman and ellipsometry maps in order to provide insights into the local donor/acceptor concentration, layer thickness and nature of the donor-acceptor interface along the direction of the thickness gradient. Deviations in spatial dependence between experimental photocurrent values and those predicted with a model assuming a sharp and well defined organic-organic interface are discussed in terms of inter-diffusion layers.

Coupling magnetic materials to plasmonic structures provides a pathway to dramatically increase the magneto-optical response of the resulting composite architecture. Although such optical enhancement has been demonstrated in a variety of systems, some basic aspects are scarcely known. In particular, reflectance/transmission modulations and electromagnetic field intensification, both triggered by plasmon excitations, can contribute to the magneto-optical enhancement. However, a quantitative evaluation of the impact of both factors on the magneto-optical response is lacking. To address this issue, we have measured magneto-optical Kerr spectra on corrugated gold/dielectric interfaces with magnetic (nickel and iron oxide) nanoparticles. We find that the magneto-optical activity is enhanced by up to an order of magnitude for wavelengths that are correlated to the excitation of propagating or localized surface plasmons. Our work sheds light on the fundamental principles for the observed optical response and demonstrates that the outstanding magneto-optical performance is originated by the increase of the polarization conversion efficiency, whereas the contribution of reflectance modulations is negligible.

We report on an organic photodiode configuration based on a donor/acceptor bilayer with opposed complementary thickness gradients. We rely on the strong dependence of the optical field on thickness to achieve spatially dependent spectral responses, a proof-of-concept for position sensitive detection. Ratiometric photocurrent values at two wavelengths allow for position determination independently of the light intensity with a spatial resolution below 600 μm.

The main challenges toward massive fabrication of silicon nanowires are the way to control the crystal orientation and size. In the present work, we report advances in the pattern transfer process to obtain arrays of holes on a Si substrate, aiming at the fabrication of ordered arrays of quantum wires. The wires obtained from this procedure can be uniform in terms of doping profile, crystal orientation and size, while enormously simplifying metallic contacting for applications where parallel biasing is needed. The samples have been fabricated using a combination of electron-beam lithography and reactive-ion etching. Electron-beam lithography is performed at 10keV on a 100nm thick 950K PMMA. A specific recipe for deep reactive-ion etching was developed in order to minimize any widening or under-etching of the holes, as well as any type of wall roughness. Holes with diameters from 30nm up to 900nm, and pitch from 90nm up to 1000nm were fabricated, achieving no observable scalloping. The sample has been oxidized for further reduction of the size of interconnects (the site between two holes) and interstitials (the site between three holes). As a result, thin nanowires have been fabricated.