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Quantum emitters hosted in crystalline lattices are highly attractive candidates for quantum information processing, secure networks and nanosensing. For many of these applications it is necessary to have control over single emitters with long spin coherence times. Such single quantum systems have been realized using quantum dots, colour centres in diamond, dopants in nanostructures and molecules . More recently, ensemble emitters with spin dephasing times on the order of microseconds and room-temperature optically detectable magnetic resonance have been identified in silicon carbide (SiC), a compound being highly compatible to up-to-date semiconductor device technology. So far however, the engineering of such spin centres in SiC on single-emitter level has remained elusive. Here, we demonstrate the control of spin centre density in ultrapure SiC over 8 orders of magnitude, from below $10^{9}$ to above $10^{16} \,$cm$^{-3}$ using neutron irradiation. For a low irradiation dose, a fully photostable, room-temperature, near infrared (NIR) single photon emitter can clearly be isolated, demonstrating no bleaching even after $10^{14}$ excitation cycles. Based on their spectroscopic fingerprints, these centres are identified as silicon vacancies, which can potentially be used as qubits, spin sensors and maser amplifiers., Comment: 5 pages, 4 figures

We investigate effects of the local structure on the excitonic transport in C60 thin films by means of temperature-dependent photoluminescence quenching studies in a range of 5 to 300 K. Exciton motion in the X-ray amorphous layers indicates thermally activated transport initiated above 80 K accompanied by a thermalization of excitations into low lying states within the excitonic density of states. Discontinuities in the temperature-dependent photoluminescence behavior can be attributed to a continuous phase transition at 80 K and a first order phase transition at 180 K, thereby revealing structural information on the local film morphology in the C60 films.

We present an investigation of the microscopic interplay between excitons and charge carriers by means of combined photoluminescence (PL) and charge carrier transport measurements on organic thin film transistors (OTFT). For this purpose, the prototypical organic semiconductor Diindenoperylene (DIP) was utilized as active material. The OTFT accumulation layer provides a spatially defined interaction zone for charges and photo-generated excitons leading to a PL intensity reduction of up to 4.5%. This effect correlates with the accumulated hole carrier density and provides a lower estimate of about 1.3E-10 cm3/s for the cross-section of non-radiative exciton-hole processes. It is rationalized that these processes are preferentially mediated by trapped holes.

In this work we address the microscopic effects related to the implementation of a Bathophenanthroline (BPhen) exciton blocking layer (EBL) sandwiched between Ag cathode and molecular Diindenoperylene (DIP)/C60 bilayer of a photovoltaic cell. Complementary studies of current density, external quantum efficiency, and photoluminescence quenching for EBL thicknesses up to 50 nm indicate that Ag atoms are able to penetrate through the whole 35 nm thick C60 film into the crystalline DIP layer underneath, thereby enhancing exciton quenching if no blocking layer is applied. In contrast, an optimal trade-off between exciton blocking, suppression of metal penetration and electron transport is achieved for a 5 nm thick BPhen layer yielding an improvement of power conversion efficiency by more than a factor of 2., Comment: This paper has been withdrawn by the author due to publication of an improved version: Steindamm et al., Appl. Phys. Lett. 101, 143302 (2012)

The exciton dynamics on flat (001) rubrene crystal surfaces have been compared with those under confined pyramidal geometry by time-resolved photoluminescence with micrometer spatial resolution. The luminescence spectra can be interpreted in terms of generation of a free and a self-trapped exciton. Their ratio depends significantly on the structural size which we explain by the optical absorption profile of the pyramids in combination with the exciton diffusion constant. For the latter a lower limit of 0.2 cm2/s at 4 K has been estimated. Temperature-dependent decay times reveal activation barriers between free and self-trapped exciton of 3 meV and 14 meV., Comment: 4 pages, 4 figures

We report on a systematic study of electronic transport in tetracene single crystals by means of space charge limited current spectroscopy and time of flight measurements. Both $I$-$V$ and time of flight measurements show that the room-temperature effective hole-mobility reaches values close to $\mu \simeq 1$ cm$^2$/Vs and show that, within a range of temperatures, the mobility increases with decreasing temperature. The experimental results further allow the characterization of different aspects of the tetracene crystals. In particular, the effects of both deep and shallow traps are clearly visible and can be used to estimate their densities and characteristic energies. The results presented in this paper show that the combination of $I$-$V$ measurements and time of flight spectroscopy is very effective in characterizing several different aspects of electronic transport through organic crystals., Comment: Accepted by J. Appl. Phys.; tentatively scheduled for publication in the January 15, 2004 issue; minor revisions compared to previous cond-mat version