Searcharxiv⌕ Search

arXiv subjects

Martin H. Dehn

Publications and source records attributed to Martin H. Dehn.

9 recordsLinked to original sources

Beyond-classical computation in quantum simulation

Quantum computers hold the promise of solving certain problems that lie beyond the reach of conventional computers. However, establishing this capability, especially for impactful and meaningful problems, remains a central challenge. Here, we show that superconducting quantum annealing processors can rapidly generate samples in close agreement with solutions of the Schrödinger equation. We demonstrate area-law scaling of entanglement in the model quench dynamics of two-, three-, and infinite-dimensional spin glasses, supporting the observed stretched-exponential scaling of effort for matrix-product-state approaches. We show that several leading approximate methods based on tensor networks and neural networks cannot achieve the same accuracy as the quantum annealer within a reasonable time frame. Thus, quantum annealers can answer questions of practical importance that may remain out of reach for classical computation.

quant-ph↗

Lithium-ion dynamics in synthetic quartz studied via the NMR of implanted $^{8}$Li$^{+}$

We report $β$-detected nuclear magnetic resonance ($β$-NMR) measurements of implanted $^{8}$Li$^{+}$ in a synthetic single crystal of $α$-SiO$_2$ (quartz). At 6.55 Tesla, the spectrum is comprised of a large amplitude broad resonance and a quadrupolar multiplet that is only revealed by an RF comb excitation. The quadrupole splitting is surprisingly small, increases with temperature, and provides information on the implantation site. Supercell density functional theory calculations show that the small EFG is consistent with an in-channel interstitial site (Wyckoff 3$a$). The spin-lattice relaxation is unexpectedly fast and strongly temperature dependent with a diffusive peak above 200 K and a second more prominent relaxation peak at lower temperature. Analysis of the diffusive relaxation yields an activation barrier 178(43) meV for the isolated Li$^{+}$, in the range of other measurements and calculations. To account for many of the other features of the data, it is suggested that some of the implanted ions trap an electron forming the neutral Li$^{0}$, which is stable over a narrow range of temperatures.

cond-mat.mtrl-sci↗

Ion-Implanted $^8$Li Nuclear Magnetic Resonance in Highly Oriented Pyrolytic Graphite

We report $β$-detected nuclear magnetic resonance of ultra-dilute $^{8}$Li$^{+}$ implanted in highly oriented pyrolytic graphite (HOPG). The absence of motional narrowing and diffusional spin-lattice relaxation implies Li$^+$ is not appreciably mobile up to 400 K, in sharp contrast to the highly lithiated stage compounds. However, the relaxation is remarkably fast and persists down to cryogenic temperatures. Ruling out extrinsic paramagnetic impurities and intrinsic ferromagnetism, we conclude the relaxation is due to paramagnetic centers correlated with implantation. While the resulting effects are not consistent with a Kondo impurity, they also differ from free paramagnetic centers, and we suggest that a resonant scattering approach may account for much of the observed phenomenology.

cond-mat.mtrl-sci↗

Depth-resolved measurement of the Meissner screening profile in a niobium thin film from spin-lattice relaxation of the implanted $β$-emitter $^{8}$Li

We report measurements of the Meissner screening profile in a Nb(300 nm)/Al$_{2}$O$_{3}$ thin film using $^{8}$Li $β$-detected nuclear magnetic resonance ($β$-NMR). The NMR probe $^{8}$Li was ion-implanted into the Nb film at energies $\leq$ 20 keV, corresponding to mean stopping depths comparable to Nb's magnetic penetration depth $λ$. $^{8}$Li's strong dipole-dipole coupling with the host $^{93}$Nb nuclei provided a "cross-relaxation" channel that dominated in low magnetic fields, which conferred indirect sensitivity to the local magnetic field via the spin-lattice relaxation (SLR) rate $1/T_{1}$. From a fit of the $1/T_{1}$ data to a model accounting for its dependence on temperature, magnetic field, and $^{8}$Li$^{+}$ implantation energy, we obtained a magnetic penetration depth $λ_{0}$ = 51.5(22) nm, consistent with a relatively short carrier mean-free-path $\ell$ = 18.7(29) nm typical of similarly prepared Nb films. The results presented here constitute an important step towards using $^{8}$Li $β$-NMR to characterize bulk Nb samples with engineered surfaces, which are often used in the fabrication of particle accelerators.

cond-mat.mtrl-sci↗

Nuclear magnetic resonance of ion implanted $^8$Li in ZnO

We report on the stability and magnetic state of ion implanted $^8$Li in single crystals of the semiconductor ZnO using $β$-detected nuclear magnetic resonance. At ultradilute concentrations, the spectra reveal distinct Li sites from 7.6 to 400 K. Ionized shallow donor interstitial Li is stable across the entire temperature range, confirming its ability to self-compensate the acceptor character of its (Zn) substitutional counterpart. Above 300 K, spin-lattice relaxation indicates the onset of correlated local motion of interacting defects, and the spectra show a site change transition from disordered configurations to substitutional. Like the interstitial, the substitutional shows no resolved hyperfine splitting, indicating it is also fully ionized above 210 K. The electric field gradient at the interstitial $^8$Li exhibits substantial temperature dependence with a power law typical of non-cubic metals.

cond-mat.mtrl-sci↗

The dynamics of liquid 1-ethyl-3-methylimidazolium acetate measured with implanted-ion $^8$Li $β$-NMR

We demonstrate the application of implanted-ion $β$-detected NMR as a probe of ionic liquid molecular dynamics through the measurement of $^8$Li spin-lattice relaxation (SLR) and resonance in 1-ethyl-3-methylimidazolium acetate. The motional narrowing of the resonance, and the local maxima in the SLR rate, $1/T_1$, imply a sensitivity to sub-nanosecond Li$^+$ solvation dynamics. From an analysis of $1/T_1$, we extract an activation energy ${E_A = 74.8 \pm 1.5}$ meV and Vogel-Fulcher-Tammann constant ${T_{\mathrm{VFT}} = 165.8 \pm 0.9}$ K, in agreement with the dynamic viscosity of the bulk solvent. Near the melting point, the lineshape is broad and intense, and the form of the relaxation is non-exponential, reflective of our sensitivity to heterogeneous dynamics near the glass transition. The depth resolution of this technique may later provide a unique means of studying nanoscale phenomena in ionic liquids.

cond-mat.soft↗

Local Metallic and Structural Properties of the Strongly Correlated Metal LaNiO$_{3}$ using $^{8}$Li $β$-NMR

We report $β$-detected NMR of ion-implanted $^{8}$Li in a single crystal and thin film of the strongly correlated metal LaNiO$_{3}$. In both samples, spin-lattice relaxation measurements reveal two distinct local metallic environments, as is evident from $T$-linear Korringa $1/T_{1}$ below 200 K with slopes comparable to other metals. A small, approximately temperature independent Knight shift of $\sim 74$ ppm is observed, yielding a normalized Korringa product characteristic of substantial antiferromagnetic correlations, but, we find no evidence for a magnetic transition from 4 to 310 K. Two distinct, equally abundant $^{8}$Li sites is inconsistent with the widely accepted rhombohedral structure of LaNiO$_{3}$, but cannot be simply explained by either of the common alternative orthorhombic or monoclinic distortions.

cond-mat.str-el↗

Ionic and electronic properties of the topological insulator Bi$_2$Te$_2$Se investigated using $β$-detected nuclear magnetic relaxation and resonance of $^8$Li

We report measurements on the high temperature ionic and low temperature electronic properties of the 3D topological insulator Bi$_2$Te$_2$Se using ion-implanted $^8$Li $β$-detected nuclear magnetic relaxation and resonance. With implantation energies in the range 5-28 keV, the probes penetrate beyond the expected range of the topological surface state, but are still within 250 nm of the surface. At temperatures above ~150 K, spin-lattice relaxation measurements reveal isolated $^8$Li$^{+}$ diffusion with an activation energy $E_{A} = 0.185(8)$ eV and attempt frequency $τ_{0}^{-1} = 8(3) \times 10^{11}$ s$^{-1}$ for atomic site-to-site hopping. At lower temperature, we find a linear Korringa-like relaxation mechanism with a field dependent slope and intercept, which is accompanied by an anomalous field dependence to the resonance shift. We suggest that these may be related to a strong contribution from orbital currents or the magnetic freezeout of charge carriers in this heavily compensated semiconductor, but that conventional theories are unable to account for the extent of the field dependence. Conventional NMR of the stable host nuclei may help elucidate their origin.

cond-mat.mtrl-sci↗

Microscopic Dynamics of Li$^{+}$ in Rutile TiO$_{2}$ Revealed by $^{8}$Li $β$-detected NMR

We report measurements of the dynamics of isolated $^{8}$Li$^{+}$ in single crystal rutile TiO$_{2}$ using $β$-detected NMR. From spin-lattice relaxation and motional narrowing, we find two sets of thermally activated dynamics: one below 100 K; and one at higher temperatures. At low temperature, the activation barrier is $26.8(6)$ meV with prefactor $1.23(5) \times 10^{10}$ s$^{-1}$. We suggest this is unrelated to Li$^{+}$ motion, and rather is a consequence of electron polarons in the vicinity of the implanted $^{8}$Li$^{+}$ that are known to become mobile in this temperature range. Above 100 K, Li$^{+}$ undergoes long-range diffusion as an isolated uncomplexed cation, characterized by an activation energy and prefactor of $0.32(2)$ eV and $1.0(5) \times 10^{16}$ s$^{-1}$, in agreement with macroscopic diffusion measurements. These results in the dilute limit from a microscopic probe indicate that Li$^{+}$ concentration does not limit the diffusivity even up to high concentrations, but that some key ingredient is missing in the calculations of the migration barrier. The anomalous prefactors provide further insight into both Li$^{+}$ and polaron motion.

cond-mat.mtrl-sci↗