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Abby N. Neill

Publications and source records attributed to Abby N. Neill.

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Hysteresis without coexistence: disorder-rounded first-order transitions in a van der Waals magnet

Quenched disorder can profoundly modify phase transitions. In low-dimensional systems, theory predicts that even weak quenched disorder can round the thermodynamic discontinuities associated with a first-order phase transition. Here, we employ time-domain terahertz spectroscopy to investigate the quasi-two-dimensional trimerized kagome van der Waals magnet family Nb$_3$Cl$_{8-x}$Br$_x$ ($x=0$, 1 and 8). We observe the emergence of an additional phonon branch upon Br substitution, whose spectral weight increases and frequency softens with increasing Br concentration. The temperature evolution of the phonon frequencies reveals a clean first-order transition in Nb$_3$Cl$_8$ characterized by macroscopic phase coexistence and thermal hysteresis. In contrast, the transition in the substitutionally disordered compound Nb$_3$Cl$_7$Br retains its hysteresis while exhibiting a substantially broadened transition with no resolvable macroscopic phase coexistence. These observations reveal disorder-induced fragmentation of the transition into locally favored domains instead of well-defined bulk phases separated by stable phase boundaries. The behavior is consistent with the Imry-Wortis and the Aizenman-Wehr scenarios for the effect of quenched disorder in low-dimensional systems, which destabilizes macroscopic phase coexistence and rounds the thermodynamic discontinuities associated with first-order transitions. Thermal hysteresis persists in the disordered compound despite the lack of resolvable coexistence, indicating that the two features often treated as a single hallmark of first-order character arise distinctly and can be separated by disorder. Moreover, our results establish Nb$_3$Cl$_{8-x}$Br$_x$ as a promising platform for investigating the effects of disorder on first-order transitions in low-dimensional systems.

cond-mat.str-el

Stripping Symmetry: Electrochemical Oxidation to a Superconducting Polar Metal in Au2Pb0.914P2

Polar metals and noncentrosymmetric superconductors are exceptionally rare, yet their broken inversion symmetry can give rise to emergent electronic phenomena including mixed singlet-triplet superconducting pairing. As only a few such materials have been found among known compounds, accessing new examples requires synthetic strategies that go beyond conventional crystal growth. Here, we use electrochemical topotactic deintercalation to remove Pb from the centrosymmetric parent compound Au$_2$PbP$_2$, producing the polar metal Au$_2$Pb$_{0.914}$P$_2$. Unlike conventional chemical doping, this transformation actively drives structural symmetry-breaking: the partial removal of Pb triggers a cooperative electronic and geometric rearrangement, mediated by a second-order Jahn-Teller effect and stereochemically active lone pairs, that locks the product into a polar, noncentrosymmetric superspace group Ama2(01g)ss0. We solve the complete (3+1)D modulated structure by synchrotron single-crystal X-ray diffraction and confirm the polar assignment through nonlinear electronic transport. Below T$_c$ = 1.52 K, Au$_2$Pb$_{0.914}$P$_2$ becomes a type-II superconductor whose heat capacity and AC susceptibility both exhibit power-law behavior, suggestive of a gap structure governed by the broken inversion symmetry of the host lattice. This work establishes electrochemical oxidation as a rational route to metastable noncentrosymmetric superconductors through chemically directed symmetry-breaking.

cond-mat.supr-con

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