Superhard and Superconducting Bilayer Borophene.

Two-dimensional superconductors, especially the covalent metals such as borophene, have received significant attention due to their new fundamental physics, as well as potential applications. Furthermore, the bilayer borophene has recently ignited interest due to its high stability and versatile properties. Here, the mechanical and superconducting properties of bilayer-δ6 borophene are explored by means of first-principles computations and anisotropic Migdal-Eliashberg analytics. We find that the coexistence of strong covalent bonds and delocalized metallic bonds endows this structure with remarkable mechanical properties (maximum 2D-Young's modulus of ~570 N/m) and superconductivity with a critical temperature of ~20 K. Moreover, the superconducting critical temperature of this structure can be further boosted to ~46 K by applied strain, which is the highest value known among all borophenes or two-dimensional elemental materials.

A novel 2D intrinsic metal-free ferromagnetic semiconductor Si3C8 monolayer.

Metal-free magnets, a special kind of ferromagnetic (FM) material, have evolved into an important branch of magnetic materials for spintronic applications. We herein propose a silicon carbide (Si3C8) monolayer and investigate its geometric, electronic, and magnetic properties by using first-principles calculations. The thermal and dynamical stability of the Si3C8 monolayer was confirmed by ab initio molecular dynamics and phonon dispersion simulations. Our results show that the Si3C8 monolayer is a FM semiconductor with a band gap of 1.76 eV in the spin-down channel and a Curie temperature of 22 K. We demonstrate that the intrinsic magnetism of the Si3C8 monolayer is derived from pz orbitals of C atoms via superexchange interactions. Furthermore, the half-metallic state in the FM Si3C8 monolayer can be induced by electron doping. Our work not only illustrates that carrier doping could manipulate the magnetic states of the FM Si3C8 monolayer but also provides an idea to design two-dimensional metal-free magnetic materials for spintronic applications.

Defective Biphenylene as High-Efficiency Hydrogen Evolution Catalysts.

Electrocatalysts play a pivotal role in advancing the application of water splitting for hydrogen production. This research unveils the potential of defective biphenylenes as high-efficiency catalysts for the hydrogen evolution reaction. Using first-principles simulations, we systematically investigated the structure, stability, and catalytic performance of defective biphenylenes. Our findings unveil that defect engineering significantly enhances the electrocatalytic activity for hydrogen evolution. Specifically, biphenylene with a double-vacancy defect exhibits an outstanding Gibbs free energy of -0.08 eV, surpassing that of Pt, accompanied by a remarkable exchange current density of -3.08 A cm-2, also surpassing that of Pt. Furthermore, we find the preference for the Volmer-Heyrovsky mechanism in the hydrogen evolution reaction, with a low energy barrier of 0.80 eV. This research provides a promising avenue for developing novel metal-free electrocatalysts for water splitting with earth-abundant carbon elements, making a significant step toward sustainable hydrogen production.

A two-dimensional borophene monolayer with ideal Dirac nodal-line fermions.

As a relatively new member of two-dimensional materials, borophene has gained huge interest over the past years, especially in the field of discovering new topological materials, such as Dirac nodal line semimetals. Here, based on first-principles calculations, for the first time, we find a completely flat borophene monolayer (named χ2/9) with ideal Dirac nodal line states around the Fermi level. A tight-binding model using the Slater-Koster approach is proposed to demonstrate that the unique electronic feature of χ2/9 that mainly originated from the first-nearest neighbor interactions of the pz orbitals of boron. According to our symmetry analysis, the Dirac nodal line in χ2/9 is guaranteed by the out-of-plane mirror or C2 rotational symmetry and the negligible pz orbital coupling. The chemical bonding analysis reveals the rare electronic properties of this material, which can be attributed to the multicentered π bonds.

Comprehensive Screening of Halogen-Containing Oxide Double Perovskites A2BXO6 (X = Cl, Br, and I) for Photovoltaic Applications.

The new halogen-containing oxide double perovskites A2BXO6 (X = Cl, Br, and I) have attracted much attention because of their superb electronic properties in halide double perovskites and their high stability in oxide double perovskites. Herein, 408 A2BXO6 double perovskites have been systematically screened by high-throughput computation. Refer to the empirical structural factors phase diagram (t-u), which uses large-scale first-principles calculations. Fourteen stable perovskites are finally confirmed; moreover, 11 of them have never been reported before. Our results show that Ba2AgIO6 and Sr2AgIO6 are the most preferable candidates for photovoltaic applications, of which Sr2AgIO6 has balanceable electron and hole effective masses, a quasi-direct band gap, and strong optical absorption. Importantly, Sr2AgIO6 was successfully synthesized by the solution method. Our work enriches the family of double perovskites, and the tentative experimental evidence undoubtedly hints at their great potential applications in the near future.

Tuning magnetism at the two-dimensional limit: a theoretical perspective.

The discovery of two-dimensional (2D) magnetic materials provides an ideal testbed for manipulating the magnetic properties at the atomically thin and 2D limit. This review gives recent progress in the emergent 2D magnets and heterostructures, focusing on the theory side. We summarize different theoretical models, ranging from the atomic to micrometer-scale, used to describe magnetic orders. Then, the current strategies for tuning magnetism in 2D materials are further discussed, such as electric field, magnetic field, strain, optics, chemical functionalization, and spin-orbit engineering. Finally, we conclude with the future challenges and opportunities for 2D magnetism.

An ideal two-dimensional nodal-ring semimetal in tetragonal borophene oxide.

Free-standing stable two-dimensional (2D) boron monolayers, i.e., borophenes, usually settle into triangular lattices with different ratios of monoatomic vacancies. However, a stable polymorph can be drastically distinct from a free-standing one upon charge doping or on a substrate, as evidenced by the free-standing unstable hexagonal borophene that was prepared on the Al(111) substrate [Sci. Bull., 2018, 63, 282]. Moreover, 2D borophenes prefer to be oxidized to form more stable borophene oxides under ambient conditions. In this work, with the help of first-principles calculations, we propose a stable borophene oxide (t-B2O) through oxidizing the free-standing unstable T-borophene. More interestingly, t-B2O is a topological nodal-ring semimetal protected by in-plane mirror symmetry and characterized by a topological index. The energy fluctuation of the nodal ring is small and no extraneous bands are entangled with the nodal ring around the Fermi level. Two tight-binding models are developed to elucidate the orbital interactions and the formation of the nodal ring. Our work not only discovers a new ideal 2D topological nodal-ring semimetal, but the method used here also provides a fresh view in the search for 2D materials.

2D honeycomb borophene oxide: a promising anode material offering super high capacity for Li/Na-ion batteries.

Rational design of novel two-dimensional (2D) electrode materials with high capacity is crucial for the further development of Li-ion and Na-ion batteries. Herein, based on first-principles calculations, we systemically investigate Li and Na storage behaviors in the recently discovered 2D topological nodal-loop metal-the honeycomb borophene oxide (h-B2O). We show that h-B2O is an almost ideal anode material. It has good conductivity before and after Li/Na adsorption, fast ion diffusion with diffusion barrier less than 0.5 eV, low open-circuit voltage (<1 V), and small lattice change (<6.2%) during intercalation. Most remarkably, its theoretical storage capacity is extremely high, reaching up to 2137 mAh · g-1 for Li and 1425 mAh · g-1 for Na. Its Li storage capacity is more than six times higher than graphite (~372 mAh · g-1), and is almost the highest among all 2D materials discovered to date. Our results strongly suggest that 2D h-B2O is an exceedingly promising anode material for both Li- and Na-ion batteries with super high capacity.

Two-dimensional honeycomb borophene oxide: strong anisotropy and nodal loop transformation.

The search for topological semimetals is mainly focused on heavy-element compounds by following the footsteps of previous research on topological insulators, with less attention on light-element materials. However, the negligible spin orbit coupling with light elements may turn out to be beneficial for realizing topological band features. Here, using first-principles calculations, we propose a new two-dimensional light-element material-the honeycomb borophene oxide (h-B2O), which has nontrivial topological properties. The proposed structure is based on the recently synthesized honeycomb borophene on an Al (111) substrate [W. Li, L. Kong, C. Chen, J. Gou, S. Sheng, W. Zhang, H. Li, L. Chen, P. Cheng and K. Wu, Sci. Bull., 2018, 63, 282-286]. The h-B2O monolayer is completely flat, unlike the oxides of graphene or silicene. We systematically investigate the structural properties of h-B2O, and find that it has very good stability and exhibits significant mechanical anisotropy. Interestingly, the electronic band structure of h-B2O hosts a nodal loop centered around the Y point in the Brillouin zone, protected by the mirror symmetry. Furthermore, under moderate lattice strain, the single nodal loop can be transformed into two loops, each penetrating through the Brillouin zone. The loops before and after the transition are characterized by different [Doublestruck Z] × [Doublestruck Z] topological indices. Our work not only predicts a new two-dimensional material with interesting physical properties, but also offers an alternative approach to search for new topological phases in 2D light-element systems.

Cr2TiC2-based double MXenes: novel 2D bipolar antiferromagnetic semiconductor with gate-controllable spin orientation toward antiferromagnetic spintronics.

Antiferromagnetic (AF) spin devices could be one of the representative components for applications of spintronics thanks to the numerous advantages such as resistance to magnetic field perturbation, stray field-free operation, and ultrahigh device operation speed. However, detecting and manipulating the spin of AF materials is still a major challenge due to the absence of a net magnetic moment and spin degeneracy in the band structure. Bipolar antiferromagnetic semiconductors are promising solutions to these problems. Herein, using density functional theory calculations, we present asymmetrical functionalized double MXenes (Cr2TiC2FCl) that behave as a novel bipolar antiferromagnetic semiconductor (BAFS) with vanishing magnetism, in which the valence band and conduction band around the Fermi level exhibit opposite spin directions. Remarkably, gate voltage can manipulate the spin orientation of the AF Cr2TiC2FCl and lead to a transition from BAFS to half-metal antiferromagnets (HMAF). Moreover, the mixed functionalized double MXenes with various F/Cl concentrations show the BAFS feature due to the different chemical environment for the Cr atom. Our results presented herein open a new strategy towards AF spintronics and the realization of the AF spin field effect transistor.

Double Kagome Bands in a Two-Dimensional Phosphorus Carbide P2C3.

The interesting properties of Kagome bands, consisting of Dirac bands and a flat band, have attracted extensive attention. However, materials with only one Kagome band around the Fermi level cannot possess physical properties of Dirac Fermions and strong correlated Fermions simultaneously. Here, we propose a new type of band structure, double Kagome bands, which can realize coexistence of the two kinds of Fermions. Moreover, the new band structure is found to exist in a new two-dimensional material, phosphorus carbide P2C3. The carbide material shows good stability and unusual electronic properties. Strong magnetism appears in the structure by hole doping of the flat band, which results in spin splitting of the Dirac bands. The edge states induced by Dirac and flat bands coexist on the Fermi level, indicating outstanding transport characteristics. In addition, a possible route to experimentally grow P2C3 on some suitable substrates such as the Ag(111) surface is also discussed.

Three-dimensional Pentagon Carbon with a genesis of emergent fermions.

Carbon, the basic building block of our universe, enjoys a vast number of allotropic structures. Owing to its bonding characteristic, most carbon allotropes possess the motif of hexagonal rings. Here, with first-principles calculations, we discover a new metastable three-dimensional carbon allotrope entirely composed of pentagon rings. The unique structure of this Pentagon Carbon leads to extraordinary electronic properties, making it a cornucopia of emergent topological fermions. Under lattice strain, Pentagon Carbon exhibits topological phase transitions, generating a series of novel quasiparticles, from isospin-1 triplet fermions to triply degenerate fermions and further to Hopf-link Weyl-loop fermions. Its Landau level spectrum also exhibits distinct features, including a huge number of almost degenerate chiral Landau bands, implying pronounced magneto-transport signals. Our work not only discovers a remarkable carbon allotrope with highly rare structural motifs, it also reveals a fascinating hierarchical particle genesis with novel topological fermions beyond the Dirac and Weyl paradigm.

Dirac Nodal Lines and Tilted Semi-Dirac Cones Coexisting in a Striped Boron Sheet.

The enchanting Dirac fermions in graphene stimulated us to seek other 2D Dirac materials, and boron monolayers may be a good candidate. So far, a number of monolayer boron sheets have been theoretically predicted, and three have been experimentally prepared. However, none of intrinsic sheets possess Dirac electrons near the Fermi level. Herein, by means of density functional theory computations, we identified a new boron monolayer, namely, hr-sB, with two types of Dirac fermions coexisting in the sheet: One type is related to Dirac nodal lines traversing Brillouin zone (BZ) with velocities approaching 106 m/s, and the other is related to tilted semi-Dirac cones with strong anisotropy. This newly predicted boron monolayer consists of hexagon and rhombus stripes. With an exceptional stability comparable to the experimentally achieved boron sheets, it is rather optimistic to grow hr-sB on some suitable substrates such as the Ag (111) surface.

Semi-Dirac semimetal in silicene oxide.

A semi-Dirac semimetal is a material that exhibits linear band dispersion in one direction and quadratic band dispersion in the orthogonal direction and, therefore, hosts massless and massive fermions at the same point in the momentum space. While a number of interesting physical properties have been predicted in semi-Dirac semimetals, it has been rare to realize such materials in condensed matter. Based on the fact that some honeycomb materials are easily oxidized or chemically absorb other atoms, here, we theoretically propose an approach of modifying their band structures by covalent addition of group-VI elements and strain engineering. We predict a silicene oxide with the chemical formula of Si2O to be a candidate semi-Dirac semimetal. Our approach is backed by the analysis and understanding of the effect of p-orbital frustration on the band structure of graphene-like materials.

Electron and phonon properties and gas storage in carbon honeycombs.

A new kind of three-dimensional carbon allotrope, termed carbon honeycomb (CHC), has recently been synthesized [PRL 116, 055501 (2016)]. Based on the experimental results, a family of graphene networks has been constructed, and their electronic and phonon properties are studied by various theoretical approaches. All networks are porous metals with two types of electron transport channels along the honeycomb axis and they are isolated from each other: one type of channel originates from the orbital interactions of the carbon zigzag chains and is topologically protected, while the other type of channel is from the straight lines of the carbon atoms that link the zigzag chains and is topologically trivial. The velocity of the electrons can reach ∼10(6) m s(-1). Phonon transport in these allotropes is strongly anisotropic, and the thermal conductivities can be very low when compared with graphite by at least a factor of 15. Our calculations further indicate that these porous carbon networks possess high storage capacity for gaseous atoms and molecules in agreement with the experiments.

Towards three-dimensional Weyl-surface semimetals in graphene networks.

Graphene as a two-dimensional topological semimetal has attracted much attention for its outstanding properties. In contrast, three-dimensional (3D) topological semimetals of carbon are still rare. Searching for such materials with salient physics has become a new direction in carbon research. Here, using first-principles calculations and tight-binding modeling, we propose a new class of Weyl semimetals based on three types of 3D graphene networks. In the band structures of these materials, two flat Weyl surfaces appear in the Brillouin zone, which straddle the Fermi level and are robust against external strain. Their unique atomic and electronic structures enable applications in correlated electronics, as well as in energy storage, molecular sieves, and catalysis. When the networks are cut, the resulting slabs and nanowires remain semimetallic with Weyl lines and points at the Fermi surfaces, respectively. Between the Weyl lines, flat surface bands emerge with possible strong magnetism. The robustness of these structures can be traced back to a bulk topological invariant, ensured by the sublattice symmetry, and to the one-dimensional Weyl semimetal behavior of the zigzag carbon chain.

Fluorine-Doped and Partially Oxidized Tantalum Carbides as Nonprecious Metal Electrocatalysts for Methanol Oxidation Reaction in Acidic Media.

A nonprecious metal electrocatalyst based on fluorine-doped tantalum carbide with an oxidative surface on graphitized carbon (TaCx FyOz/(g)C) is developed by using a simple one-pot in situ ion exchange and adsorption method, and the TaCxFyOz/(g)C shows superior performance and durability for methanol oxidation reaction and extreme tolerance to CO poisoning in acidic media.