Publications by authors named "von Bardeleben HJ"

High-spin defects (color centers) in wide-gap semiconductors are considered as a basis for the implementation of quantum technologies due to the unique combination of their spin, optical, charge, and coherent properties. A silicon carbide (SiC) crystal can act as a matrix for a wide variety of optically active vacancy-type defects, which manifest themselves as single-photon sources or spin qubits. Among the defects, the nitrogen-vacancy centers () are of particular importance.

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As the development of aluminum-ion batteries is still in its infancy, researchers are still dedicated to exploring suitable host materials and investigating their aluminum intercalation behaviours. Here, a series of cyanido-bridged chain compounds with the formula {[Fe(Tp)(CN)][M(HO)]} (M = Ni, Co, Mn, Zn, Cu) are studied as cathode electrodes for aluminum-ion batteries with [EMIm]Cl-AlCl (1-ethyl-3-methylimidazolium chloride-AlCl) ionic liquid as the electrolyte. The electrochemical properties suggested Fe/Fe to be the redox-active couple during the aluminum intercalation and deintercalation processes of these compounds, and the observed maximum specific capacity obtained by the Fe-Co compound is 200 mA h g despite the rapid specific capacity fading.

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FeCo Prussian blue analogues of general formula ACo[Fe(CN)] are responsive, non-stoichiometric materials whose magnetic and optical properties can be reversibly switched by light irradiation. However, elucidating the critical influence of the inserted alkali ion, A, on the material's properties remains complicated due to their complex local structure. Here, by investigating soluble A ⊂ [Fe-Co] cyanido cubes (A = K, Rb, and Cs), both accurate structural and electronic information could be obtained.

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Silicon carbide (SiC) has become a key player in the realization of scalable quantum technologies due to its ability to host optically addressable spin qubits and wafer-size samples. Here, we have demonstrated optically detected magnetic resonance (ODMR) with resonant excitation and clearly identified the ground state energy levels of the NV centers in 4H-SiC. Coherent manipulation of NV centers in SiC has been achieved with Rabi and Ramsey oscillations.

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We report the enhancement of the optical emission between 850 and 1400 nm of an ensemble of silicon mono-vacancies (V), silicon and carbon divacancies (VV), and nitrogen vacancies (NV) in an n-type 4H-SiC array of micropillars. The micropillars have a length of ca. 4.

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Octahedral molecular sieves (OMS) are built of transition metal-oxygen octahedra that delimit sub-nanoscale cavities. Compared to other microporous solids, OMS exhibit larger versatility in properties, provided by various redox states and magnetic behaviors of transition metals. Hence, OMS offer opportunities in electrochemical energy harnessing devices, including batteries, electrochemical capacitors and electrochromic systems, provided two conditions are met: fast exchange of ions in the micropores and stability upon exchange.

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Single-photon emitters (SPEs) play an important role in a number of quantum information tasks such as quantum key distributions. In these protocols, telecom wavelength photons are desired due to their low transmission loss in optical fibers. In this paper, we present a study of bright single-photon emitters in cubic silicon carbide (3C-SiC) emitting in the telecom range.

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We show experimental evidence of magnetization switching in a single (Ga,Mn)(As,P) semiconducting ferromagnetic layer, attributed to a strong reduction of the magnetization and the anisotropy due to current injection. The nucleation of magnetization reversal is found to occur even in the absence of a magnetic field and to be both anisotropic and stochastic. Our findings highlight a new mechanism of magnetization manipulation based on spin accumulation in a semiconductor material.

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Combining electron paramagnetic resonance, density functional theory, and positron annihilation spectroscopy (PAS), we identify the nitrogen interstitial defect in GaN. The isolated interstitial is unstable and transforms into a split interstitial configuration (N-N)(N). It is generated by particle irradiation with an introduction rate of a primary defect, pins the Fermi level at E(C)-1.

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Intrinsic paramagnetic defects in ∼5 nm sized nanodiamonds, produced by various dynamic synthesis (DySND) techniques (detonation, shock-wave, pulsed laser ablation of solid carbon containing targets), have been studied by multi-frequency electron paramagnetic resonance (EPR). X-band (9-10 GHz) EPR spectra of DySND, in addition to the main intensive singlet Lorentzian-like EPR signal, reveal a low intensity doublet pattern within the half-field (HF) region (g ∼ 4). On transferring spectra to the Q-band (34 GHz) the shape of the HF pattern changes and splitting between doublet components is reduced from 10.

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We report the observation of a paramagnetic interface defect in thermally oxidized porous n-type doped 4H-SiC/SiO(2). Based on its axial symmetry and resolved hyperfine interactions it is attributed to an sp(3) carbon dangling bond center situated at the SiC side of the interface. This center is electrically active and pins the Fermi level in the oxidized samples.

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