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The discovery of new high-temperature superconductors is one of the most critical problems in materials, chemistry, and physics. This work systematically investigates fluorite-like structures of XBeH8 (X is Ac, Th, Pa, U, and Np) to gain physical insight into the pressure effects on the properties. Our results reveal that AcBeH8 and ThBeH8 are two potential high-temperature superconductors, where AcBeH8 reaching a superconducting transition temperature of 284.11 K at 150 GPa and even a value of 203.29 K at 50 GPa, ThBeH8 has Tc is 217.65 K at 200 GPa, and the predicted results provide strong candidates for achieving high temperature or even room temperature superconductivity. The analysis of pressure effects demonstrates unusual charge transfer and atomic structure in the system, with s-f migration in Ac/Th atoms and s-p migration in Be atoms, similar to the high-pressure behavior of alkaline earth metals. In the past long time, superconductivity and magnetism were considered unable to coexist. However, UBeH8 and NpBeH8 are two potential magnetic superconductors with maximum Tc of 60.70 and 107.18 K at 100 and 350 GPa, respectively, and Hubbard U calculations predict their magnetic moments with 1.52 to 1.90 and 2.49 to 2.92 muB at 0 K. The coexistence of magnetic and superconducting states may be attributed to the different sublattice actions.

Metallic hydrogen is capable of showing room temperature superconductivity, but its experimental syntheses are extremely hard. Therefore, it is desirable to reduce the synthesis pressure of metallic hydrogen by adding other chemical elements. However, for most hydrides, the metallization of hydrogen by "chemical precompression" to achieve high-temperature superconductivity still requires relatively high pressure, making experimental synthesis difficult. How to achieve high-temperature superconductivity in the low-pressure range (0-50 GPa) is a key issue for realizing practical applications of superconducting materials. Toward this end, this work proposes a strategy for inserting ammonium ions in the fcc crystal of metals. High-throughput calculations of the periodic table reveal 12 elements which can form kinetically stable and superconducting hydrides at low pressures, where the highest superconducting transition temperatures of AlN2H8, MgN2H8 and GaN2H8 can reach up to 118.40, 105.09 and 104.39 K. Pressure-induced bond length changes and charge transfer reveal the physical mechanism of high-temperature superconductivity, where the H atom continuously gains electrons leading to the transition of H+ ions to atomic H, facilitating metallization of hydrogen under mild pressure. Our results also reveal two strong linear scalar relationships, one is the H-atom charge versus superconducting transition temperature and the other is the first ionization energy versus the highest superconducting transition temperature. Besides, ZnN2H8, CdN2H8, and HgN2H8 were found to be superconductors at ambient pressure, and the presence of interstitial electrons suggests that they are also electrides, whose relatively low work functions (3.03, 2.78, and 3.05 eV) imply that they can be used as catalysts for nitrogen reduction reactions as well.

Inorganic electrides are a new class of compounds catering to the interest of scientists due to the multiple usages exhibited by interstitial electrons in the lattice. However, the influence of the shape and distribution of interstitial electrons on physical properties and new forms of physical states are still unknown. In this work, crystal structure search algorithms are employed to explore the possibility of forming new electrides in the As-Li system, where interstitial electrons behave as 1D electron chains (1D electride) in Pmmm phase of AsLi$_7$ and transform into 0D electron clusters (0D electride) in P6/mmm phase at 80 GPa. The P6/mmm phase has relatively high superconductivity at 150 GPa (Tc=38.4K) than classical electrides, even at moderate pressure with Tc=16.6K. The novel superconducting properties are conjectured to be possibly due to three Van Hove singularities at the Fermi level. In addition, a Dirac cone in the band has been observed, expanding the sources of Dirac materials. The survival of AsLi$_7$ at room temperature is confirmed by molecular dynamics simulation at 300 K. At 1000 K, the As atoms in the system act like solid, while a portion of the Li atoms cycle around the As atoms, and another portion of the Li atoms flow freely like liquid, showing the novel physical phenomenon of the coexistence of the plastic and superionic states. This suggests that the superionic and plastic states cannot only be found in hydrides but also in the electride. Our results indicate that superconducting electride AsLi$_7$ with superionic and plastic states can exist in Earth's interior.

Recently, electrides have received increasing attention due to their multifunctional properties as superconducting, catalytic, insulating, and electrode materials, with potential to offer other performance and possess novel physical states. This work uncovers that Li$_5$N as an electride possess four novel physical states simultaneously: electride state, super-coordinated state, superconducting state, and superionic state. By obtaining high-pressure phase diagrams of the Li-N system at 150-350 GPa using a crystal structure search algorithm, we find that Li$_5$N can remain stable as P6/mmm structure and has a 14-fold super-coordination number, as verified by Bader charge and electron localization function analysis. Aditionally, we find that its superconducting transition temperature decreases continuously with increasing pressure, contrary to the behavior of most high-pressure superconducting materials. Its superconducting transition temperature reaches the highest among all known electride at 150 GPa (Tc = 48.97 K). Besides, Li$_5$N exhibits the superionic state at 3000 K, in which N atoms act like solid, while some Li atoms flow like liquid. The above results are further verified at a macroscopic level by using deep learning potential molecular dynamics simulations.

We report a combined experimental and theoretical study on intriguing magnetic properties of quasiferroelectric orthochromates. Large single crystals of the family of RECrO$_3$ (RE = Y, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) compounds were successfully grown. Neutron Laue study indicates a good quality of the obtained single crystals. Applied magnetic-field and temperature dependent magnetization measurements reveal their intrinsic magnetic properties, especially the antiferromagnetic (AFM) transition temperatures. Density functional theory studies of the electronic structures were carried out using the Perdew-Burke-Ernzerhof functional plus Hubbard $U$ method. Crystallographic information and magnetism were theoretically optimized systematically. When RE$^{3+}$ cations vary from Y$^{3+}$ and Eu$^{3+}$ to Lu$^{3+}$ ions, the calculated $t$-$e$ orbital hybridization degree and N\'{e}el temperature behave similarly to the experimentally-determined AFM transition temperature with variation in cationic radius. We found that the $t$-$e$ hybridization is anisotropic, causing a magnetic anisotropy of Cr$^{3+}$ sublattices. This was evaluated with the nearest-neighbour $J_1$-$J_2$ model. Our research provides a picture of the electronic structures during the $t$-$e$ hybridization process while changing RE ions and sheds light on the nature of the weak ferromagnetism coexisting with predominated antiferromagnetism. The available large RECrO$_3$ single crystals build a platform for further studies of orthochromates., Comment: 22 pages, 12 figures, 3 tables