arXiv subjects

Danna E. Freedman

Publications and source records attributed to Danna E. Freedman.

6 recordsLinked to original sources

arXiv2025

A general and modular approach to solid-state integration and readout of zero-dimensional quantum systems

Here, we present an all-electrical readout mechanism for quasi-0D quantum states (0D-QS) such as point defects, adatoms and molecules, that is modular and general, providing an approach that is amenable to scaling and integration with other solid-state quantum technologies. Our approach relies on the crea-tion of high-quality tunnel junctions via the mechanical exfoliation and stacking of multi-layer gra-phene (MLG) and hexagonal boron nitride (hBN) to encapsulate the target system in an MLG/hBN/0D-QS/hBN/MLG heterostructure. This structure allows for all-electronic spectroscopy and readout of candidate systems through a combination of coulomb and spin-blockade. As a proof of principle, we demonstrate electronic tunneling spectroscopy of point defects in hBN and the molecular qubit vanadyl phthalocyanine (VOPc). Our approach demonstrates a new pathway for the incorporation of molecules and atomic defects into solid-state quantum devices and circuits along with a readout scheme that does not rely on highly-constrained optical processes for photonic readout.

cond-mat.mtrl-sci↗

arXiv2025

Symmetry-mediated quantum coherence of $W^{5+}$ spins in an oxygen-deficient double perovskite

Elucidating the factors limiting quantum coherence in real materials is essential to the development of quantum technologies. Here we report a strategic approach to determine the effect of lattice dynamics on spin coherence lifetimes using oxygen deficient double perovskites as host materials. In addition to obtaining millisecond $T_1$ spin-lattice lifetimes at T ~ 10 K, measurable quantum superpositions were observed up to room temperature. We determine that $T_2$ enhancement in $Sr_2CaWO_{6-δ}$ over previously studied $Ba_2CaWO_{6-δ}$ is caused by a dynamically-driven increase in effective site symmetry around the dominant paramagnetic site, assigned as $W^{5+}$ via electron paramagnetic resonance spectroscopy. Further, a combination of experimental and computational techniques enabled quantification of the relative strength of spin-phonon coupling of each phonon mode. This analysis demonstrates the effect of thermodynamics and site symmetry on the spin lifetimes of $W^{5+}$ paramagnetic defects, an important step in the process of reducing decoherence to produce longer-lived qubits.

cond-mat.mtrl-sci↗

arXiv2023

Quantum sensing of magnetic fields with molecular color centers

Molecular color centers, such as $S=1$ Cr($o$-tolyl)$_{4}$, show promise as an adaptable platform for magnetic quantum sensing. Their intrinsically small size, i.e., 1-2 nm, enables them to sense fields at short distances and in various geometries. This feature, in conjunction with tunable optical read-out of spin information, offers the potential for molecular color centers to be a paradigm shifting materials class beyond diamond-NV centers by accessing a distance scale opaque to NVs. This capability could, for example, address ambiguity in the reported magnetic fields arising from two-dimensional magnets by allowing for a single sensing technique to be used over a wider range of distances. Yet, so far, these abilities have only been hypothesized with theoretical validation absent. We show through simulation that Cr($o$-tolyl)$_{4}$ can spatially resolve proximity-exchange versus direct magnetic field effects from monolayer CrI$_{3}$ by quantifying how these interactions impact the excited states of the molecule. At short distances, proximity exchange dominates through molecule-substrate interactions, but at further distances the molecule behaves as a typical magnetic sensor, with magnetostatic effects dominating changes to the energy of the excited state. Our models effectively demonstrate how a molecular color center could be used to measure the magnetic field of a 2D magnet and the role different distance-dependent interactions contribute to the measured field.

cond-mat.mtrl-sci↗

arXiv2020

Pressure induced collapse of magnetic order in jarosite

We report a pressure-induced phase transition in the frustrated kagomé material jarosite at ~45 GPa, which leads to the disappearance of magnetic order. Using a suite of experimental techniques, we characterize the structural, electronic, and magnetic changes in jarosite through this phase transition. Synchrotron powder X-ray diffraction and Fourier transform infrared spectroscopy experiments, analyzed in aggregate with the results from density functional theory calculations, indicate that the material changes from a R-3m structure to a structure with a R-3c space group. The resulting phase features a rare twisted kagomé lattice in which the integrity of the equilateral Fe3+ triangles persists. Based on symmetry arguments we hypothesize that the resulting structural changes alter the magnetic interactions to favor a possible quantum paramagnetic phase at high pressure.

cond-mat.mtrl-sci↗

arXiv2020

Introduction of spin centers in single crystals of Ba$_2$CaWO$_{6-δ}$

Developing the field of quantum information science (QIS) hinges upon designing viable qubits, the smallest unit in quantum computing. One approach to creating qubits is introducing paramagnetic defects into semiconductors or insulators. This class of qubits has seen success in the form of nitrogen-vacancy centers in diamond, divacancy defects in SiC, and P doped into Si. These materials feature paramagnetic defects in a low nuclear spin environment to reduce the impact of nuclear spin on electronic spin coherence. In this work, we report single crystal growth of Ba$_2$CaWO$_{6-δ}$, and the coherence properties of controllably introduced W$^{5+}$ spin centers generated by oxygen vacancies. Ba$_2$CaWO$_{6-δ}$ ($δ$ = 0) is a B-site ordered double perovskite with a temperature-dependent octahedral tilting wherein oxygen vacancies generate W$^{5+}$ (d$^1$), $S = \frac{1}{2}, I$ = 0, centers. We characterized these defects by measuring the spin-lattice ($T_1$) and spin-spin relaxation ($T_2$) times from T = 5 to 150 K. At T = 5 K, $T_1$ = 310 ms and $T_2$ = 4 $μ$s, establishing the viability of these qubit candidates. With increasing temperature, $T_2$ remains constant up to T = 60 K and then decreases to $T_2$ $\approx$ 1 $μ$s at T = 90 K, and remains roughly constant until T = 150 K, demonstrating the remarkable stability of $T_2$ with increasing temperature. Together, these results demonstrate that controlled defect generation in double perovskite structures can generate viable paramagnetic point centers for quantum applications and expand the field of potential materials for QIS.

cond-mat.mtrl-sci↗

arXiv2014

Thermodynamic Properties of the Quantum Spin Liquid Candidate ZnCu$_{3}$(OH)$_{6}$Cl$_{2}$ in High Magnetic Fields

We report measurements of the specific heat and magnetization of single crystal samples of the spin-1/2 kagome compound ZnCu$_{3}$(OH)$_{6}$Cl$_{2}$ (herbertsmithite), a promising quantum spin-liquid candidate, in high magnetic fields and at low temperatures. The magnetization was measured up to $μ_{0}H$ = 55 T at $T$ = 0.4 K, showing a saturation of the weakly interacting impurity moments in fields above $\sim10$ T. The specific heat was measured down to $T < 0.4$ K in magnetic fields up to 18 T, revealing $T$-linear and $T$-squared contributions. The $T$-linear contribution is surprisingly large and indicates the presence of gapless excitations in large applied fields. These results further highlight the unusual excitation spectrum of the spin liquid ground state of herbertsmithite.

cond-mat.str-el↗