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Hans-Gerd Boyen

Publications and source records attributed to Hans-Gerd Boyen.

4 recordsLinked to original sources

Long Spin Relaxation Times in CVD-Grown Nanodiamonds

Currently, the primary applications of fluorescent nanodiamonds (FNDs) are in the area of biosensing, by using photoluminescence or spin properties of colour centres, mainly represented by the Nitrogen Vacancy (NV) point defect. The sensitivity of NV-FNDs to external fields is, however, limited by crystallographic defects, which influence their key quantum state characteristics - the spin longitudinal (\textit{T$_1$}) and spin transversal (\textit{T$_2$}) relaxation and coherence times, respectively. We report on utilising an advanced FND growth technique consisting of heterogeneous nucleation on pre-engineered sites to create FNDs averaging around 60 nm in size, with mean longitudinal coherence times of 800 $\mu$s and a maximum over 1.8 ms, close to bulk theoretical values. This is a major, nearly ten-fold improvement over commercially available nanodiamonds for the same size range of 50 to 150 nm. Heavy-N doped nanodiamond shells, important for sensing events in nm proximity to the diamond surface, are fabricated and discussed in terms of re-nucleation and twinning on \{111\} crystal facets. We also discuss scalability issues in order to enable the production of FND volumes matching the needs of sensing applications.

cond-mat.mes-hall

Magnetic characterization of oblique angle deposited Co/CoO on gold nanoparticles

The influence of a patterned substrate on obliquely deposited, exchange biased Co/CoO films was studied. It was found that substrates decorated with nanoparticle patterns provide the option to manipulate the orientation of the magnetic easy axis in obliquely deposited thin films. The complementary methods of SQUID magnetometry and polarized neutron reflectometry were used to disentangle the different contributions to the magnetic hysteresis of such complex magnetic systems.

cond-mat.mtrl-sci

Perovskite-perovskite tandem photovoltaics with optimized bandgaps

We demonstrate four and two-terminal perovskite-perovskite tandem solar cells with ideally matched bandgaps. We develop an infrared absorbing 1.2eV bandgap perovskite, $FA_{0.75}Cs_{0.25}Sn_{0.5}Pb_{0.5}I_3$, that can deliver 14.8 % efficiency. By combining this material with a wider bandgap $FA_{0.83}Cs_{0.17}Pb(I_{0.5}Br_{0.5})_3$ material, we reach monolithic two terminal tandem efficiencies of 17.0 % with over 1.65 volts open-circuit voltage. We also make mechanically stacked four terminal tandem cells and obtain 20.3 % efficiency. Crucially, we find that our infrared absorbing perovskite cells exhibit excellent thermal and atmospheric stability, unprecedented for Sn based perovskites. This device architecture and materials set will enable 'all perovskite' thin film solar cells to reach the highest efficiencies in the long term at the lowest costs.

cond-mat.mtrl-sci

Transition from anomalous kinetics towards Fickian diffusion for Si dissolution into amorphous Ge

Over the last years several experimental and theoretical studies of diffusion kinetics on the nanoscale have shown that the time evolution differs from the classical Fickian law (kc=0.5). However, all work was based on crystalline samples or models, so far. In this letter, we report on the diffusion kinetics of a thin amorphous-Si layer into amorphous-Ge to account for the rising importance of amorphous materials in nanodevices. Employing surface sensitive technics, the initial kc was found at 0.7+-0.1. Moreover, after some monolayers of Si dissolved into the Ge, kc changes to the generally expected classical Fickian law with kc=0.5.

cond-mat.mtrl-sci