PandaX is a large upgradable liquid-xenon detector system that can be used for both direct dark-matter detection and $^{136}$Xe double-beta decay search. It is located in the Jinping Deep-Underground Laboratory in Sichuan, China. The detector operate
s in dual-phase mode, allowing detection of both prompt scintillation, and ionization charge through proportional scintillation. The central time projection chamber will be staged, with the first stage accommodating a target mass of about 120,kg. In stage II, the target mass will be increased to about 0.5,ton. In the final stage, the detector can be upgraded to a multi-ton target mass. In this paper a detailed description of the stage-I detector design and performance results established during the commissioning phase is presented.
We synthesize and study single crystals of a new double-perovskite Sr2YIrO6. Despite two strongly unfavorable conditions for magnetic order, namely, pentavalent Ir5+(5d4) ions which are anticipated to have Jeff=0 singlet ground states in the strong s
pin-orbit coupling (SOC) limit, and geometric frustration in a face centered cubic structure formed by the Ir5+ ions, we observe this iridate to undergo a novel magnetic transition at temperatures below 1.3 K. We provide compelling experimental and theoretical evidence that the origin of magnetism is in an unusual interplay between strong non-cubic crystal fields and intermediate-strength SOC. Sr2YIrO6 provides a rare example of the failed dominance of SOC in the iridates.
We report the successful synthesis of single-crystals of the layered iridate, (Na$_{1-x}$Li$_{x}$)$_2$IrO$_3$, $0leq x leq 0.9$, and a thorough study of its structural, magnetic, thermal and transport properties. The new compound allows a controlled
interpolation between Na$_2$IrO$_3$ and Li$_2$IrO$_3$, while maintaing the novel quantum magnetism of the honeycomb Ir$^{4+}$ planes. The measured phase diagram demonstrates a dramatic suppression of the Neel temperature, $T_N$, at intermediate $x$ suggesting that the magnetic order in Na$_2$IrO$_3$ and Li$_2$IrO$_3$ are distinct, and that at $xapprox 0.7$, the compound is close to a magnetically disordered phase that has been sought after in Na$_2$IrO$_3$ and Li$_2$IrO$_3$. By analyzing our magnetic data with a simple theoretical model we also show that the trigonal splitting, on the Ir$^{4+}$ ions changes sign from Na$_2$IrO$_3$ and Li$_2$IrO$_3$, and the honeycomb iridates are in the strong spin-orbit coupling regime, controlled by $jeff=1/2$ moments.
We report calorimetric, magnetic and electric transport properties of single-crystal CaRuO3 and SrRuO3 as a function of temperature T and applied magnetic field B. We find that CaRuO3 is a non-Fermi-liquid metal near a magnetic instability, as charac
terized by the following properties: (1) the heat capacity C(T,B) ~ -T log T is readily enhanced in low applied fields, and exhibits a Schottky peak at 2.3 K that exhibits field dependence when T is reduced; (2) the magnetic susceptibility diverges as T^-x at low temperatures with 1/2 < x < 1, depending on the applied field; and (3) the electrical resistivity exhibits a T3/2 dependence over the range 1.7 < T < 24 K. No Shubnikov-de Haas oscillations are discerned at T = 0.65 K for applied fields up to 45 T. These properties, which sharply contrast those of the itinerant ferromagnet SrRuO3, indicate CaRuO3 is a rare example of a stoichiometric oxide compound that exhibits non-Fermi-liquid behavior near a quantum critical point.
The spin valve effect is a quantum phenomenon so far only realized in multilayer thin films or heterostructures. Here we report a strong spin valve effect existing in bulk single crystals of Ca3(Ru1-xCrx)2O7 having an anisotropic, bilayered crystal s
tructure. This discovery opens new avenues to understand the underlying physics of spin valves, and fully realize its potential in practical devices.
We report transport and thermodynamic properties of single-crystal SrIrO3 as a function of temperature T and applied magnetic field H. We find that SrIrO3 is a non-Fermi-liquid metal near a ferromagnetic instability, as characterized by the following
properties: (1) small ordered moment but no evidence for long-range order down to 1.7 K; (2) strongly enhanced magnetic susceptibility that diverges as T or T1/2 at low temperatures, depending on the applied field; (3) heat capacity C(T,H) ~ -Tlog T that is readily amplified by low applied fields; (4) a strikingly large Wilson ratio at T< 4K; and (5) a T3/2-dependence of electrical resistivity over the range 1.7 < T < 120 K. A phase diagram based on the data implies SrIrO3 is a rare example of a stoichiometric oxide compound that exhibits non-Fermi-liquid behavior near a quantum critical point (T = 0 and H = 0.23 T).
