arXiv subjects

G. Alexander Smith

Publications and source records attributed to G. Alexander Smith.

7 recordsLinked to original sources

arXiv2026

Superconducting dome due to the Fano-Feshbach shape resonance in artificial high-Tc superlattices

In this work we provide compelling experimental validation of the Bianconi Perali Valletta (BPV) theory predicting a superconducting dome based on a quantum material design of Artificial High TC Superlattices (AHTS) made with a selected nanoscale heterostructure geometry. These AHTS are SNSN superlattices of quantum wells of period d, composed of first units, superconducting doped Mott insulator layers with Rashba spin orbit coupling (S) of thickness L, intercalated by second units, normal metal spacers (N). In these superlattices, grown by molecular beam epitaxy (MBE), the experimental superconducting dome is obtained by material quantum design changing the chemical potential via the quantum geometrical factor L/d which tunes the Fano-Feshbach shape resonance in the pair transfer between superconducting gaps in the BCS regime and different gaps in the BEC-BCS crossover. Here we present a systematic magneto-transport study of AHTS artificial superlattices across the full doping range of the superconducting dome, from the deeply underdoped to the overdoped regime, using pulsed magnetic fields up to 72 T. By varying the L/d ratio, we tune the effective hole concentration delta=0.45(1-L/d) and map the evolution of the resistive transitions, the upper critical magnetic field and the Ginzburg-Landau coherence length

cond-mat.supr-con↗

arXiv2026

High magnetic field response of superconductivity dome in quantum artificial High Tc superlattices with variable geometry

It is known that cuprate artificial high Tc superlattices (AHTS) with period d, composed of quantum wells confining interface space charge in stoichiometric Mott insulator layers (S), with thickness L, at the interface with overdoped normal metallic cuprate layers (N) show a superconducting dome by tuning the geometric L over d ratio of the SNSN superlattice with the top predicted by quantum material design engineering quantum size effects. Here we report high-field magneto transport measurements up to 41 Tesla of AHTS across the entire superconducting dome. The results show the universal upward-concave behavior of the temperature dependent upper critical magnetic field in low Tc samples at rising edge and drop edge of the dome providing strong evidence consistent with two-band superconductivity for two-band superconductivity in agreement with multigap theory used for quantum design of the SNSN superlattices. The measured superconducting coherence length demonstrates that atomic-scale engineering controls not only the critical temperature but also the intrinsic pair size at Fano-Feshbach resonances physics paving the way toward next generation quantum devices and shedding light on unconventional superconductivity.

cond-mat.supr-con↗

arXiv2025

Long-Term Stability of Superconducting Metal Superhydrides

Zhou et al., in their recent publication (Nat. Commun. 16, 1135, 2025), reported the synthesis of lanthanum superhydride, LaHx (x = 10.2-11.1), by laser heating LaH3 with NH3BH3 at a pressure of 170 GPa and investigated the temporal evolution of the NMR spectra of the reaction products. They observed a gradual decrease in the 1H-NMR signal intensity assigned to the synthesized metal hydride, accompanied by an increase in molecular hydrogen within the sample chamber over a period of 50 days. Based on these observations, the authors concluded that LaH10 progressively decomposes into LaH3 and H2 within two months after synthesis at its formation pressure of 170 GPa. Here, we demonstrate that, under their formation conditions, metal superhydrides are thermodynamically more stable than metal trihydrides. Furthermore, we present direct experimental evidence - based on X-ray diffraction and four-probe electrical resistance measurements - confirming the stability of both the crystal lattice and high-temperature superconducting properties of the Fm-3m-LaH10 phase for more than five years. This long-term stability is consistent with predictions from quantum chemistry calculations.

cond-mat.supr-con↗

arXiv2023

Ultra-fast yttrium hydride chemistry at high pressures via non-equilibrium states induced by x-ray free electron laser

Controlling the formation and stoichiometric content of desired phases of materials has become a central interest for the study of a variety of fields, notably high temperature superconductivity under extreme pressures. The further possibility of accessing metastable states by initiating reactions by x-ray triggered mechanisms over ultra-short timescales is enabled with the development of x-ray free electron lasers (XFEL). Utilizing the exceptionally high brilliance x-ray pulses from the EuXFEL, we report the synthesis of a previously unobserved yttrium hydride under high pressure, along with non-stoichiometric changes in hydrogen content as probed at a repetition rate of 4.5\,MHz using time-resolved x-ray diffraction. Exploiting non-equilibrium pathways we synthesize and characterize a hydride with yttrium cations in an \textit{A}15 structure type at 125\,GPa, predicted using crystal structure searches, with a hydrogen content between 4.0--5.75 hydrogens per cation, that is enthalpically metastable on the convex hull. We demonstrate a tailored approach to changing hydrogen content using changes in x-ray fluence that is not accessible using conventional synthesis methods, and reveals a new paradigm in metastable chemical physics.

cond-mat.mtrl-sci↗

arXiv2023

Observation of Conventional Near Room Temperature Superconductivity in Carbonaceous Sulfur Hydride

The phenomenon of high temperature superconductivity, approaching room temperature, has been realized in a number of hydrogen-dominant alloy systems under high pressure conditions1-12. A significant discovery in reaching room temperature superconductivity is the photo-induced reaction of sulfur, hydrogen, and carbon that initially forms of van der Waals solids at sub-megabar pressures. Carbonaceous sulfur hydride has been demonstrated to be tunable with respect to carbon content, leading to different superconducting final states with different structural symmetries. A modulated AC susceptibility technique adapted for a diamond anvil cell confirms a Tc of 260 kelvin at 133 GPa in carbonaceous sulfur hydride. Furthermore, direct synchrotron infrared reflectivity measurements on the same sample under the same conditions reveal a superconducting gap of ~85 meV at 100 K in close agreement to the expected value from Bardeen-Cooper-Schrieffer (BCS) theory13-18. Additionally, x-ray diffraction in tandem with AC magnetic susceptibility measurements above and below the superconducting transition temperature, and as a function of pressure at 107-133 GPa, reveal the Pnma structure of the material is responsible for the close to room-temperature superconductivity at these pressures.

cond-mat.supr-con↗

arXiv2021

Lower pressure phases and metastable states of superconducting photo-induced carbonaceous sulfur hydride

Room-temperature superconductivity was recently discovered in carbonaceous sulfur hydride (C-S-H) close to 3\,Mbar. We report significant differences in the superconducting response of C-S-H, with a maximum $T_{C}$ of 191(1)\,K, below a 1\,Mbar. Variations in intensity of the C-H Raman modes reveal carbon content can vary between crystals synthesized with the same photo-induced method. Synchrotron single crystal x-ray diffraction identifies polymorphism with increasing degrees of covalency. These unique metastable states are highly sensitive to thermodynamic pathways.

cond-mat.supr-con↗

arXiv2018

Post-aragonite phases of CaCO$_{3}$ at lower mantle pressures

The stability, structure and properties of carbonate minerals at lower mantle conditions has significant impact on our understanding of the global carbon cycle and the composition of the interior of the Earth. In recent years, there has been significant interest in the behavior of carbonates at lower mantle conditions, specifically in their carbon hybridization, which has relevance for the storage of carbon within the deep mantle. Using high-pressure synchrotron X-ray diffraction in a diamond anvil cell coupled with direct laser heating of CaCO$_{3}$ using a CO$_{2}$ laser, we identify a crystalline phase of the material above 40 GPa $-$ corresponding to a lower mantle depth of around 1,000 km $-$ which has first been predicted by \textit{ab initio} structure predictions. The observed $sp^{2}$ carbon hybridized species at 40 GPa is monoclinic with $P2_{1}/c$ symmetry and is stable up to 50 GPa, above which it transforms into a structure which cannot be indexed by existing known phases. A combination of \textit{ab initio} random structure search (AIRSS) and quasi-harmonic approximation (QHA) calculations are used to re-explore the relative phase stabilities of the rich phase diagram of CaCO$_{3}$. Nudged elastic band (NEB) calculations are used to investigate the reaction mechanisms between relevant crystal phases of CaCO$_{3}$ and we postulate that the mineral is capable of undergoing $sp^{2}$-$sp^{3}$ hybridization change purely in the $P2_{1}/c$ structure $-$ forgoing the accepted post-aragonite $Pmmn$ structure.

cond-mat.mtrl-sci↗