arXiv subjects

Z. Gai

Publications and source records attributed to Z. Gai.

14 recordsLinked to original sources

arXiv2023

Rare $^{40}$K decay with implications for fundamental physics and geochronology

Potassium-40 is a widespread, naturally occurring isotope whose radioactivity impacts subatomic rare-event searches, nuclear structure theory, and estimated geological ages. A predicted electron-capture decay directly to the ground state of argon-40 has never been observed. The KDK (potassium decay) collaboration reports strong evidence of this rare decay mode. A blinded analysis reveals a non-zero ratio of intensities of ground-state electron-captures ($I_{\text{EC}^0}$) over excited-state ones ($I_\text{EC*}$) of $ I_{\text{EC}^0} / I_\text{EC*} = 0.0095 \stackrel{\text{stat}}{\pm} 0.0022 \stackrel{\text{sys}}{\pm} 0.0010 $ (68% C.L.), with the null hypothesis rejected at 4$σ$. In terms of branching ratio, this signal yields $I_{\text{EC}^0} = 0.098\% \stackrel{\text{stat}}{\pm} 0.023\% \stackrel{\text{sys}}{\pm} 0.010\% $, roughly half of the commonly used prediction, with consequences for various fields [L. Hariasz et al., companion paper, DOI: 10.1103/PhysRevC.108.014327].

nucl-ex↗

arXiv2023

Evidence for ground-state electron capture of $^{40}$K

Potassium-40 is a widespread isotope whose radioactivity impacts estimated geological ages spanning billions of years, nuclear structure theory, and subatomic rare-event searches - including those for dark matter and neutrinoless double-beta decay. The decays of this long-lived isotope must be precisely known for its use as a geochronometer, and to account for its presence in low-background experiments. There are several known decay modes for $^{40}$K, but a predicted electron-capture decay directly to the ground state of argon-40 has never been observed, while theoretical predictions span an order of magnitude. The KDK Collaboration reports on the first observation of this rare decay, obtained using a novel combination of a low-threshold X-ray detector surrounded by a tonne-scale, high-efficiency $γ$-ray tagger at Oak Ridge National Laboratory. A blinded analysis reveals a distinctly nonzero ratio of intensities of ground-state electron-captures ($I_{\text{EC}^0}$) over excited-state ones ($I_{\text{EC}^*}$) of $I_{\text{EC}^0} / I_{\text{EC}^*}=0.0095\stackrel{\text{stat}}{\pm}0.0022\stackrel{\text{sys}}{\pm}0.0010$ (68% CL), with the null hypothesis rejected at 4$σ$ [Stukel et al., DOI:10.1103/PhysRevLett.131.052503]. This unambiguous signal yields a branching ratio of $I_{\text{EC}^0}=0.098\%\stackrel{\text{stat}}{\pm}0.023\%\stackrel{\text{sys}}{\pm}0.010$, roughly half of the commonly used prediction. This first observation of a third-forbidden unique electron capture improves understanding of low-energy backgrounds in dark-matter searches and has implications for nuclear-structure calculations. A shell-model based theoretical estimate for the $0νββ$ decay half-life of calcium-48 is increased by a factor of $7^{+3}_{-2}$. Our nonzero measurement shifts geochronological ages by up to a percent; implications are illustrated for Earth and solar system chronologies.

nucl-ex↗

arXiv2021

A novel experimental system for the KDK measurement of the $^{40}$K decay scheme relevant for rare event searches

Potassium-40 ($^{40}$K) is a long-lived, naturally occurring radioactive isotope. The decay products are prominent backgrounds for many rare event searches, including those involving NaI-based scintillators. $^{40}$K also plays a role in geochronological dating techniques. The branching ratio of the electron capture directly to the ground state of argon-40 has never been measured, which can cause difficulty in interpreting certain results or can lead to lack of precision depending on the field and analysis technique. The KDK (Potassium (K) Decay (DK)) collaboration is measuring this decay. A composite method has a silicon drift detector with an enriched, thermally deposited $^{40}$K source inside the Modular Total Absorption Spectrometer. This setup has been characterized in terms of energy calibration, gamma tagging efficiency, live time and false negatives and positives. A complementary, homogeneous, method is also discussed; it employs a KSr$_2$I$_5$:Eu scintillator as source and detector.

physics.ins-det↗

arXiv2020

Superconductivity with Tc=7 K under pressure for Cu-, and Au-doped BaFe2As2

It is noteworthy that chemical substitution of BaFe2As2 (122) with the noble elements Cu and Au gives superconductivity with a maximum Tc=3 K, while Ag substitution (Ag-122) stays antiferromagnetic. For Ba(Fe1-xTMx)2As2, TM= Cu, Au, or Ag, and by doping an amount of x=0.04, a-lattice parameter slightly increases (0.4%) for all TM dopants, while c-lattice decreases (-0.2%) for TM=Cu, barely moves (0.05%) for Au, and increases (0.2%) for Ag. Despite the naive expectation that the noble elements of group 11 should affect the quantum properties of 122 similarly, they produce significant differences extending to the character of the ground state. For the Ag-122 crystal, evidence of only a filamentary superconductivity is noted with pressure. However, for Au and Cu doping (x=0.03) we find a substantial improvement in the superconductivity, with Tc increasing to 7 K and 7.5 K, respectively, under 20 kbar of pressure. As with the ambient pressure results, the identity of the dopant therefore has a substantial impact on the ground state properties. Density functional theory calculations corroborate these results and find evidence of strong electronic scattering for Au and Ag dopants, while Cu is comparatively less disruptive to the 122 electronic structure.

cond-mat.supr-con↗

arXiv2019

Local Superconductivity in Vanadium Iron Arsenide

We investigate the chemical substitution of group 5 into BaFe2As2 (122) iron arsenide, in the effort to understand why Fe-site hole doping of this compound (e.g., using group 5 or 6) does not yield bulk superconductivity. We find an increase in c-lattice parameter of the BaFe2As2 with the substitution of V, Nb, or Ta; the reduction in c predicts the lack of bulk superconductivity [1] that is confirmed here through transport and magnetization results. However, our spectroscopy measurements find a coexistence of antiferromagnetic and local superconducting nanoscale regions in V-122, observed for the first time in a transition-metal hole-doped iron arsenide. In BaFe2As2, there is a complex connection between local parameters such as composition and lattice strain, average lattice details, and the emergence of bulk quantum states such as superconductivity and magnetism. [1] L. M. N. Konzen, and A. S. Sefat, J. Phys.: Condens. Matter 29 (2017), 083001.

cond-mat.supr-con↗

arXiv2017

The KDK (potassium decay) experiment

Potassium-40 (${}^{40}$K) is a background in many rare-event searches and may well play a role in interpreting results from the DAMA dark-matter search. The electron-capture decay of ${}^{40}$K to the ground state of ${}^{40}$Ar has never been measured and contributes an unknown amount of background. The KDK (potassium decay) collaboration will measure this branching ratio using a ${}^{40}$K source, an X-ray detector, and the Modular Total Absorption Spectrometer at Oak Ridge National Laboratory.

nucl-ex↗

arXiv2017

Magnetic ground state of the Ising-like antiferromagnet DyScO$_3$

We report the low temperature magnetic properties of the DyScO$_3$ perovskite, which were characterized by means of single crystal and powder neutron scattering, and by magnetization measurements. Below $T_{\mathrm{N}}=3.15$ K, Dy$^{3+}$ moments form an antiferromagnetic structure with an easy axis of magnetization lying in the $ab$-plane. The magnetic moments are inclined at an angle of $\sim\pm{28}^{\circ}$ to the $b$-axis. We show that the ground state Kramers doublet of Dy$^{3+}$ is made up of primarily $|\pm 15/2\rangle$ eigenvectors and well separated by crystal field from the first excited state at $E_1=24.9$ meV. This leads to an extreme Ising single-ion anisotropy, $M_{\perp}/M_{\|}\sim{0.05}$. The transverse magnetic fluctuations, which are proportional to $M^{2}_{\perp}/M^{2}_{\|}$, are suppressed and only moment fluctuations along the local Ising direction are allowed. We also found that the Dy-Dy dipolar interactions along the crystallographic $c$-axis are 2-4 times larger than in-plane interactions.

cond-mat.str-el↗

arXiv2017

Full Electroresistance Modulation in a Mixed-Phase Metallic Alloy

We report a giant, ~22%, electroresistance modulation for a metallic alloy above room temperature. It is achieved by a small electric field of 2 kV/cm via piezoelectric strain-mediated magnetoelectric coupling and the resulting magnetic phase transition in epitaxial FeRh/BaTiO3 heterostructures. This work presents detailed experimental evidence for an isothermal magnetic phase transition driven by tetragonality modulation in FeRh thin films, which is in contrast to the large volume expansion in the conventional temperature-driven magnetic phase transition in FeRh. Moreover, all the experimental results in this work illustrate FeRh as a mixed-phase model system well similar to phase-separated colossal magnetoresistance systems with phase instability therein.

cond-mat.mtrl-sci↗

arXiv2016

Improving quantum-transition temperatures in BaFe2As2-based crystals by removing local-lattice strain & electronic-structure disorder

Quantum materials such as antiferromagnets or superconductors are complex in that chemical, electronic, and spin phenomena at atomic scales can manifest in their collective properties. Although there are some clues for designing such materials, they remain mainly unpredictable. In this work, we find that enhancement of transition temperatures in BaFe2As2-based crystals are caused by removing local-lattice strain and electronic-structure disorder by thermal annealing. While annealing improves Neel-ordering temperature in BaFe2As2 crystal (TN=132 K to 136 K) by removing in-plane electronic defects and overall reduction of a-lattice parameter, it increases superconducting-ordering temperature in optimally cobalt-doped BaFe2As2 crystal (Tc=23 to 25 K) by precipitating-out the cobalt dopants and giving larger overall a-lattice parameter. Although annealing promotes local chemical and electronic uniformity resulting in higher TN in the parent, it results in nanoscale phase separation in the superconductor resulting in lower disparity and strong superconducting band gaps in the dominant crystalline regions, which lead to both higher overall Tc and critical-current-density, Jc.

cond-mat.supr-con↗

arXiv2014

Strain driven anisotropic magnetoresistance in antiferromagnetic La$_{0.4}$Sr$_{0.6}$MnO$_{3}$

We investigate the effects of strain on antiferromagntic (AFM) single crystal thin films of La$_{1-x}$Sr$_{x}$MnO$_{3}$ (x = 0.6). Nominally unstrained samples have strong magnetoresistance with anisotropic magnetoresistances (AMR) of up to 8%. Compressive strain suppresses magnetoresistance but generates AMR values of up to 63%. Tensile strain presents the only case of a metal-insulator transition and demonstrates a previously unreported AMR behavior. In all three cases, we find evidence of magnetic ordering and no indication of a global ferromagnetic phase transition. These behaviors are attributed to epitaxy induced changes in orbital occupation driving different magnetic ordering types. Our findings suggest that different AFM ordering types have a profound impact on the AMR magnitude and character.

cond-mat.str-el↗

arXiv2014

Tuning the metal-insulator transition in manganite films through surface exchange coupling with magnetic nanodots

In strongly correlated electronic systems, such as manganites, the global transport behavior depends sensitively on the spin ordering, whose alteration often requires a large external magnetic field. Here we show that the spin ordering in manganites can be easily controlled by exchange field across the interface between a ferromagnet and a manganite. By depositing isolated ferromagnetic nanodots on a manganite thin film, we find that it is possible to overcome dimensionality and strain effects to raise the metal-insulator transition (MIT) temperature by over 200 K and increase the magnetoresistance by 5000%. The MIT temperature can also be tuned by controlling the density of the magnetic nanodots which indicates that the formation process of electronic phase separation can be controlled by the presence of magnetic nanodots.

cond-mat.str-el↗

arXiv2013

Jeff=1/2 Mott spin-orbit insulating state close to the cubic limit in Ca4IrO6

The Jeff=1/2 state is manifested in systems with large cubic crystal field splitting and spin-orbit coupling that are comparable to the on-site Coulomb interaction, U. 5d transition metal oxides host parameters in this regime and strong evidence for this state in Sr2IrO4, and additional iridates, has been presented. All the candidates, however, deviate from the cubic crystal field required to provide an unmixed canonical Jeff=1/2 state, impacting the development of a robust model of this novel insulating and magnetic state. We present results that not only show Ca4IrO6 hosts the state, but furthermore uniquely resides close to the ideal case required for an unmixed Jeff=1/2 state.

cond-mat.str-el↗

arXiv2012

Magnetic structural change of Sr2IrO4 upon Mn doping

The layered 5d transition metal oxide Sr2IrO4 has been shown to host a novel Jeff=1/2 Mott spin orbit insulating state with antiferromagnetic ordering, leading to comparisons with the layered cuprates. Here we study the effect of substituting Mn for Ir in single crystals of Sr2Ir0.9Mn0.1O4 through an investigation involving bulk measurements and resonant x-ray and neutron scattering. We observe a new long range magnetic structure emerge upon doping through a reordering of the spins from the basal plane to the c-axis with a reduced ordering temperature compared to Sr2IrO4. The strong enhancement of the magnetic x-ray scattering intensity at the L3 edge relative to the L2 edge indicates that the Jeff=1/2 state is robust and capable of hosting a variety of ground states.

cond-mat.str-el↗

arXiv2012

Dynamics of a first order electronic phase transition in manganites

By reducing an electronically phase separated manganite (La[1-y]Pr[y])[x]Ca[1-x]MnO3 single crystal thin film to dimensions on the order of the inherent phase domains, it is possible to isolate and monitor the behavior of single domains at a first order transition. At this critical point, it is possible to study the coexistence, formation and annihilation processes of discrete electronic phase domains. With this technique, we make several new observations on the mechanisms leading to the metal insulator transition in manganites. We observe that domain formation is emergent and random, the transition process from the metallic phase to the insulating phase takes longer than the reverse process, electric field effects are more influential in driving a phase transition than current induced electron heating, and single domain transition dynamics can be tuned through careful application of temperature and electric field.

cond-mat.mtrl-sci↗