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Wolfgang Harneit

Bio: Wolfgang Harneit is an academic researcher from University of Osnabrück. The author has contributed to research in topics: Endohedral fullerene & Fullerene. The author has an hindex of 23, co-authored 66 publications receiving 1981 citations. Previous affiliations of Wolfgang Harneit include Helmholtz-Zentrum Berlin & Free University of Berlin.


Papers
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Journal ArticleDOI
TL;DR: In this article, an alternative concept for a scalable spin quantum computer that combines aspects of other proposals with the advantageous features of endohedral fullerenes was proposed, where electron spins instead of nuclear spins are used and that the manipulation of fullerene molecules is fairly easy.
Abstract: We propose an alternative concept for a scalable spin quantum computer that combines aspects of other proposals with the advantageous features of endohedral fullerenes. The key advantages are that electron spins instead of nuclear spins are used and that the manipulation of fullerene molecules is fairly easy. Qubits are set and read out via pulsed electron-spin resonance. Addressing is provided by local magnetic fields or field gradients $(A$ gate). The qubit-qubit interaction is mediated by magnetic dipolar coupling and can be controlled via the direction of the magnetic field with respect to the distance vector of the qubits $(J$ gate). Molecular as well as solid-state architectures are discussed.

287 citations

Journal ArticleDOI
TL;DR: In order to measure the resonance frequency in real time, a field-frequency lock is applied to the optically detected magnetic resonance signal of a single electron spin in a nanodiamond using a Zeeman splitting of a localized single spin.
Abstract: The Zeeman splitting of a localized single spin can be used to construct a highly sensitive magnetometer offering almost atomic spatial resolution. While sub-$\ensuremath{\mu}\mathrm{T}$ sensitivity can be obtained in principle using pulsed techniques and long measurement times, a fast and easy method without laborious data postprocessing is desirable for a scanning-probe approach with high spatial resolution. In order to measure the resonance frequency in real time, we applied a field-frequency lock to the optically detected magnetic resonance signal of a single electron spin in a nanodiamond. We achieved a sampling rate of up to 100 readings per sec with a sensitivity of $6\text{ }\text{ }\ensuremath{\mu}\mathrm{T}/\sqrt{\mathrm{Hz}}$. Images of the field distribution around a magnetic wire were acquired with $\ensuremath{\sim}30\text{ }\text{ }\ensuremath{\mu}\mathrm{T}$ resolution and 4096 submicron sized pixels in 10 min. The response of several spins was used to reconstruct the field orientation.

197 citations

Journal ArticleDOI
TL;DR: A room-temperature implementation of the Deutsch-Jozsa algorithm is reported by encoding both a qubit and an auxiliary state in the electron spin of a single N-V center by exploiting the specific S=1 character of the spin system.
Abstract: The nitrogen-vacancy defect center (N-V center) is a promising candidate for quantum information processing due to the possibility of coherent manipulation of individual spins in the absence of the cryogenic requirement. We report a room-temperature implementation of the Deutsch-Jozsa algorithm by encoding both a qubit and an auxiliary state in the electron spin of a single N-V center. By thus exploiting the specific S = 1 character of the spin system, we demonstrate how even scarce quantum resources can be used for test-bed experiments on the way towards a large-scale quantum computing architecture.

139 citations

Journal ArticleDOI
TL;DR: Success is reported in making electrical contact to individual magnetic N@C(60) molecules and measuring spin excitations in their electron tunnelling spectra, and it is verified that the molecules remain magnetic.
Abstract: The manipulation of single magnetic molecules may enable new strategies for high-density information storage and quantum-state control. However, progress in these areas depends on developing techniques for addressing individual molecules and controlling their spin. Here, we report success in making electrical contact to individual magnetic N@C60 molecules and measuring spin excitations in their electron tunnelling spectra. We verify that the molecules remain magnetic by observing a transition as a function of magnetic field that changes the spin quantum number and also the existence of non-equilibrium tunnelling originating from low-energy excited states. From the tunnelling spectra, we identify the charge and spin states of the molecule. The measured spectra can be reproduced theoretically by accounting for the exchange interaction between the nitrogen spin and electron(s) on the C60 cage. To enable the development of devices based on the electrical manipulation of magnetic molecules, their magnetic state needs to be conserved when electrical contacts are applied. N@C60 molecules have now been integrated as part of single-molecule transistors, and their spin states retained. This achievement may lead towards their use in high-density information storage and quantum-state control.

100 citations

Journal ArticleDOI
TL;DR: Pulsed electrically detected magnetic resonance experiments on vertical photocurrents through Al/C(60)/ZnO samples showed that an electron spin Rabi oscillation is reflected by transient current changes.
Abstract: An experimental demonstration of electrical detection of coherent spin motion of weakly coupled, localized electron spins in thin fullerene C60 films at room temperature is presented. Pulsed electrically detected magnetic resonance experiments on vertical photocurrents through Al/C(60)/ZnO samples showed that an electron spin Rabi oscillation is reflected by transient current changes. The nature of possible microscopic mechanisms responsible for this spin to charge conversion as well as its implications for the readout of endohedral fullerene (N@C(60)) spin qubits are discussed.

83 citations


Cited by
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Journal ArticleDOI
TL;DR: Here, it is demonstrated the synthesis and application of ultrapure isotopically controlled single-crystal chemical vapour deposition (CVD) diamond with a remarkably low concentration of paramagnetic impurities, and single electron spins show the longest room-temperature spin dephasing times ever observed in solid-state systems.
Abstract: As quantum mechanics ventures into the world of applications and engineering, materials science faces the necessity to design matter to quantum grade purity. For such materials, quantum effects define their physical behaviour and open completely new (quantum) perspectives for applications. Carbon-based materials are particularly good examples, highlighted by the fascinating quantum properties of, for example, nanotubes or graphene. Here, we demonstrate the synthesis and application of ultrapure isotopically controlled single-crystal chemical vapour deposition (CVD) diamond with a remarkably low concentration of paramagnetic impurities. The content of nuclear spins associated with the (13)C isotope was depleted to 0.3% and the concentration of other paramagnetic defects was measured to be <10(13) cm(-3). Being placed in such a spin-free lattice, single electron spins show the longest room-temperature spin dephasing times ever observed in solid-state systems (T2=1.8 ms). This benchmark will potentially allow observation of coherent coupling between spins separated by a few tens of nanometres, making it a versatile material for room-temperature quantum information processing devices. We also show that single electron spins in the same isotopically engineered CVD diamond can be used to detect external magnetic fields with a sensitivity reaching 4 nT Hz(-1/2) and subnanometre spatial resolution.

1,751 citations

01 Feb 1995
TL;DR: In this paper, the unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio using DFT, MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set.
Abstract: : The unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio. Harmonic force fields are obtained using Density Functional Theory (DFT), MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set. DFT calculations use the Local Spin Density Approximation (LSDA), BLYP, and Becke3LYP (B3LYP) density functionals. Mid-IR spectra predicted using LSDA, BLYP, and B3LYP force fields are of significantly different quality, the B3LYP force field yielding spectra in clearly superior, and overall excellent, agreement with experiment. The MP2 force field yields spectra in slightly worse agreement with experiment than the B3LYP force field. The SCF force field yields spectra in poor agreement with experiment.The basis set dependence of B3LYP force fields is also explored: the 6-31G* and TZ2P basis sets give very similar results while the 3-21G basis set yields spectra in substantially worse agreements with experiment. jg

1,652 citations

Journal ArticleDOI
TL;DR: Hybrid quantum circuits combine two or more physical systems, with the goal of harnessing the advantages and strengths of the different systems in order to better explore new phenomena and potentially bring about novel quantum technologies as discussed by the authors.
Abstract: Hybrid quantum circuits combine two or more physical systems, with the goal of harnessing the advantages and strengths of the different systems in order to better explore new phenomena and potentially bring about novel quantum technologies. This article presents a brief overview of the progress achieved so far in the field of hybrid circuits involving atoms, spins, and solid-state devices (including superconducting and nanomechanical systems). How these circuits combine elements from atomic physics, quantum optics, condensed matter physics, and nanoscience is discussed, and different possible approaches for integrating various systems into a single circuit are presented. In particular, hybrid quantum circuits can be fabricated on a chip, facilitating their future scalability, which is crucial for building future quantum technologies, including quantum detectors, simulators, and computers.

1,439 citations

Journal ArticleDOI
TL;DR: A concise overview of the basic properties of diamond, from synthesis to electronic and magnetic properties of embedded NV centers, and how single NV centers can be harnessed for nanoscale sensing are described, including the physical quantities that may be detected, expected sensitivities, and the most common measurement protocols.
Abstract: Crystal defects in diamond have emerged as unique objects for a variety of applications, both because they are very stable and because they have interesting optical properties. Embedded in nanocrystals, they can serve, for example, as robust single-photon sources or as fluorescent biomarkers of unlimited photostability and low cytotoxicity. The most fascinating aspect, however, is the ability of some crystal defects, most prominently the nitrogen-vacancy (NV) center, to locally detect and measure a number of physical quantities, such as magnetic and electric fields. This metrology capacity is based on the quantum mechanical interactions of the defect's spin state. In this review, we introduce the new and rapidly evolving field of nanoscale sensing based on single NV centers in diamond. We give a concise overview of the basic properties of diamond, from synthesis to electronic and magnetic properties of embedded NV centers. We describe in detail how single NV centers can be harnessed for nanoscale sensing,...

1,232 citations

Journal ArticleDOI
TL;DR: The physical principles that allow for magnetic field detection with NV centres are presented and first applications of NV magnetometers that have been demonstrated in the context of nano magnetism, mesoscopic physics and the life sciences are discussed.
Abstract: The isolated electronic spin system of the nitrogen-vacancy (NV) centre in diamond offers unique possibilities to be employed as a nanoscale sensor for detection and imaging of weak magnetic fields. Magnetic imaging with nanometric resolution and field detection capabilities in the nanotesla range are enabled by the atomic-size and exceptionally long spin-coherence times of this naturally occurring defect. The exciting perspectives that ensue from these characteristics have triggered vivid experimental activities in the emerging field of 'NV magnetometry'. It is the purpose of this article to review the recent progress in high-sensitivity nanoscale NV magnetometry, generate an overview of the most pertinent results of the last years and highlight perspectives for future developments. We will present the physical principles that allow for magnetic field detection with NV centres and discuss first applications of NV magnetometers that have been demonstrated in the context of nano magnetism, mesoscopic physics and the life sciences.

1,033 citations