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Guangtao Liu

Publications and source records attributed to Guangtao Liu.

9 recordsLinked to original sources

Room-Temperature Superconductivity at 298 K in Ternary La-Sc-H System at High-pressure Conditions

Room-temperature superconductor has been a century-long dream of humankind. Recent research on hydrogen-based superconductors (e.g., CaH6, LaH10, etc.) at high-pressure conditions lifts the record of superconducting critical temperature (Tc) up to ~250 kelvin. We here report the experimental synthesis of the first-ever room-temperature superconductor by compression on a mixture of La-Sc alloy and ammonia borane at pressures of 250-260 gigapascals (GPa) via a diamond anvil cell by a laser-heating technique. Superconductivity with an onset temperature of 271-298 kelvin at 195-266 GPa is observed by the measurement of zero electrical resistance and the suppression of Tc under applied magnetic fields. Synchrotron X-ray diffraction data unambiguously reveal that this superconductor crystallizes in a hexagonal structure with a stoichiometry LaSc2H24, in excellent agreement with our previous prediction1. Through thirteen reproducible experimental runs, we provide solid evidence of the realization of a room-temperature superconductor for the first time, marking a milestone in the field of superconductivity.

cond-mat.supr-con

Observation of molecular and polymeric nitrogen stuffed NaCl ionic layers

Sodium chloride (NaCl), a ubiquitous and chemically stable compound, has been considered inert under ambient conditions. Its typical B1 structure is highly isotropic without preferential direction, favoring the growth of a three-dimensional network of strong Na-Cl ionic bonds. Here, we employ first-principles structural searching and synchrotron X-ray diffraction to unravel an unexpected chemical reaction between NaCl and N2 to produce a hybrid salt-NaCl(N2)2, where N2 molecules break the isotropic NaCl structure into two-dimensional layers upon synthesis at 50 GPa. In contrast to the insulating properties of pristine NaCl, the electronic bandgap of the N2-stuffed NaCl narrowed to 1.8 eV, becoming an indirect bandgap semiconductor. Further compression to 130 GPa induced the polymerization of N atoms into zigzag N-chains. Our findings not only demonstrate the possibility of unusual N-chemistry under extreme conditions, but also suggest a feasible approach for the design of layered NaCl frameworks to modulate the polymerization of nitrogen.

cond-mat.mtrl-sci

Signature of superconductivity in pressurized La4Ni3O10-x single crystals grown at ambient pressure

Nickelates have attracted enormous attention since the discovery of high-temperature superconductivity in La3Ni2O7 under high pressure. However, whether superconducting nickelate single crystals can be prepared at ambient pressure remains elusive. Here we report signature of superconductivity in pressurized La4Ni3O10-x single crystals grown from potassium carbonate flux at ambient pressure. Single crystal X-ray diffraction and scanning transmission electron microscopy investigations re-vealed high-quality single crystals with perfect stacking of trilayers. Resistivity measurements indicate that the metal-to-metal transition observed at ambient pressure was suppressed under high pressure, and a sharp drop occurred at ~30 K at 77.9 GPa, consistent with superconductivity in pressurized La4Ni3O10 single crystals grown by the floating zone method at an oxygen pressure of >18 bar. Our results not only provide an important path to prepare high-quality nickelate single crystals but also support superconductivity in nickelates under high pressure, promoting more systematic and in-depth research in this compelling field.

cond-mat.supr-con

Synthesis and Superconductivity in yttrium superhydrides under high pressure

The flourishing rare earth superhydrides are a class of recently discovered materials that possess near-room-temperature superconductivity at high pressures, opening a new era of superconductivity research at high pressures. Among these superhydrides, yttrium superhydrides attracted great interest owing to their abundance of stoichiometries and excellent superconductivities. Here, we carried out a comprehensive study of yttrium superhydrides in a wide pressure range of 145-300 GPa. We successfully synthesized a series of superhydrides with the compositions of YH4, YH6, YH7, and YH9, and reported their superconducting transition temperatures of 82 K at 167 GPa, 218 K at 165 GPa, 29 K at 162 GPa, and 230 K at 300 GPa, respectively, which were evidenced by a sharp drop of resistivity. The structure and superconductivity of YH4, which was taken as a representative example, were also examined by X-ray diffraction measurements and the suppression of the superconductivity under external magnetic fields, respectively. Clathrate YH10 as a candidate of room-temperature superconductor was not synthesized within the studied pressure and temperature ranges of up to 300 GPa and 2000 K, respectively. The current work created a detailed platform for further searching room-temperature superconductors in polynary yttrium-based superhydrides.

cond-mat.supr-con

Efficient route to achieve superconductivity improvement via substitutional La-Ce alloy superhydride at high pressure

The discovery of clathrate superhydrides has approached the long-standing dream of room-temperature superconductivity and thus inspired their prosperous research under high pressure. However, how to experimentally optimize these compelling superhydrides is still a formidable challenge. Here, we find that half of the Ce atoms in the recently discovered hexagonal close packed (hcp) CeH9 structure can be randomly replaced by adjacent La, resulting in the formation of LaH9 unit that is impossible in a binary system. Our experiments show that hcp (La, Ce)H9 can be synthesized at ~110 GPa and possesses a maximum Tc of 178 K at higher pressure, which is evidenced by in-situ X-ray diffraction and electronic transport measurement where a sharp drop of resistivity to zero and a characteristic decrease of Tc under a magnetic field up to 9 T. More importantly, the Tc of (La, Ce)H9 is significantly increased by ~50-80 K compared to CeH9, showing the hitherto highest Tc at megabar pressure. Our experimental results not only verify the feasibility of improving the superconductivity of hydrides by introducing other suitable metals, but also provide important inspiration for finding high-Tc superconductors in various multinary superhydrides.

cond-mat.supr-con

High-Tc superconductivity in clathrate calcium hydride CaH6

Recent discovery of superconductive rare earth/actinide superhydrides has ushered in a new era of superconductivity research at high pressures. This distinct type of clathrate metal hydrides was first proposed for alkaline-earth-metal hydride CaH6 that, however, has long eluded experimental synthesis, impeding an understanding of pertinent physics. Here, we report successful synthesis of CaH6 and its measured superconducting critical temperature Tc of 215 K at 172 GPa, which is evidenced by a sharp drop of resistivity to zero and a characteristic decrease of Tc under a magnetic field up to 9 T.An estimate based on the Werthamer-Helfand-Hohenberg model gives a giant zero-temperature upper critical magnetic field of 203 T. These remarkable benchmark superconducting properties place CaH6 among the most outstanding high-Tc superhydrides, marking it as the hitherto only clathrate metal hydride outside the family of rare earth/actinide hydrides. This exceptional case raises great prospects of expanding the extraordinary class of high-Tc superhydrides to a broader variety of compounds that possess more diverse material features and physics characteristics.

cond-mat.supr-con

Design and Synthesis of Clathrate LaB8 with Superconductivity

Boron-based clathrate materials, typically with three-dimensional networks of B atoms, have tunable properties through substitution of guest atoms, but the tuning of B cages themselves has not yet been developed. By combining crystal structural search with the laser-heated diamond anvil cell technique, we successfully synthesized a new B-based clathrate boride, LaB8, at ~108 GPa and ~2100 K. The novel structure has a B-richest cage, with 26 B atoms encapsulating a single La atom. LaB8 demonstrates phonon-mediated superconductivity with an estimated transition temperature of 14 K at ambient pressure, mainly originating from electron-phonon coupling of B cage. This work creates a prototype platform for subsequent investigation on tunable electronic properties through the choice of captured atoms.

cond-mat.mtrl-sci

Experimental Syntheses of Sodalite-like Clathrate EuH$_6$ and EuH$_9$ at Extreme Pressures

The recent discovery of a class of sodalite-like clathrate superhydrides (e.g., YH6, YH9, ThH9, ThH10, and LaH10) at extreme pressures, which exhibit commonly a high-temperature superconductivity with the highest Tc approaching 260 K for LaH10, opened up a new era in search of high-temperature superconductors in metal superhydrides. There is a high interest towards the finding of alternative clathrate superhydrides that might witness the long-dreamed room-temperature superconductivity. Here, we target on the experimental synthesis of strongly-correlated europium (Eu) superhydrides where theory can fail for the prediction of superconductivity. We pressurized and laser-heated the mixture of metal Eu and ammonia borane (NH3BH3) in a diamond anvil cell and successfully synthesized the sodalite-like clathrate EuH6 and EuH9 at conditions of 152 GPa and 1,700 K, and 170 GPa and 2,800 K, respectively. Two non-clathrate structured phases of EuH5 and EuH6 were also synthesized that are not reported in lanthanide superhydrides. Calculated large H-derived electronic density of states at the Fermi level in clathrate EuH6 implies the potential of high temperature superconductivity. Our work created a model superhydride platform for subsequent investigation on how strongly-correlated effect in electronic structure can affect the superconductivity of superhydrides, a phenomenon that is not known thus far.

physics.chem-ph

Dehydrogenation through the pressure-induced polymerization processes of phosphine

PH3 is studied to understand the superconducting transition and responsible stoichiometry under high pressure by means of Raman, IR, and x-ray diffraction (XRD) measurements, and theoretical calculations. It is found PH3 is stable up to about 8 GPa and then starts to dehydrogenate through two dimerization processes at room temperature as pressure up to 25 GPa. Two resulting phosphorus hydrides, P2H4 and P4H6, are verified experimentally and can be recovered to ambient pressure. On further compression above 35 GPa, P4H6 directly decomposes into elemental phosphorus. The superconductivity transition temperatures of P4H6 at 100 and 200 GPa have been predicted to be 13 and 67 K in agreement with reported results, suggesting it might responsible for the superconductivity at higher pressures. Our results clearly show that P2H4 and P4H6 are only stable P-H compounds between PH3 and elemental phosphorus, shedding light on the superconducting mechanism.

cond-mat.mtrl-sci