Density functional theory (DFT) computations were performed to investigate the electronic properties and Li storage capability of Ti(3)C(2), one representative MXene (M represents transition metals, and X is either C or/and N) material, and its fluorinated and hydroxylated derivatives. The Ti(3)C(2) monolayer acts as a magnetic metal, while its derived Ti(3)C(2)F(2) and Ti(3)C(2)(OH)(2) in their stable conformations are semiconductors with small band gaps. Li adsorption forms a strong Coulomb interaction with Ti(3)C(2)-based hosts but well preserves its structural integrity. The bare Ti(3)C(2) monolayer exhibits a low barrier for Li diffusion and high Li storage capacity (up to Ti(3)C(2)Li(2) stoichiometry). The surface functionalization of F and OH blocks Li transport and decreases Li storage capacity, which should be avoided in experiments. The exceptional properties, including good electronic conductivity, fast Li diffusion, low operating voltage, and high theoretical Li storage capacity, make Ti(3)C(2) MXene a promising anode material for Li ion batteries.

The geometries, formation energies, and electronic and magnetic properties of N-doping defects, including single atom substitution and pyridine- and pyrrole-like substructures in zigzag graphene nanoribbons (ZGNRs), were investigated by means of spin-unrestricted density functional theory computations. The edge carbon atoms are more easily substituted with N atoms, and three-nitrogen vacancy (3NV) defect and four-nitrogen divacancy (4ND) defect also prefer the ribbon edge. Single N atom substitution and pyridine- and pyrrole-like N-doping defects can all break the degeneracy of the spin polarization of pristine ZGNRs. One single N atom substitution makes the antiferromagnetic semiconducting ZGNRs into spin gapless semiconductors, while double edge substitution transforms N-doped graphenes into metals. Pyridine- and pyrrole-like N-doping defects make ZGNRs into half-metals or spin gapless semiconductors. These results suggest the potential applications of N-doped ZGNRs in nanoelectronics.

In this paper, MnO2 nanomaterials of different crystallographic types and crystal morphologies have been selectively synthesized via a facile hydrothermal route and electrochemically investigated as the cathode active materials of primary and rechargeable batteries. Beta-MnO2 nano/microstructures, including one-dimensional (1-D) nanowires, nanorods, and nanoneedles, as well as 2-D hexagramlike and dendritelike hierarchical forms, were obtained by simple hydrothermal decomposition of an Mn(NO3)2 solution under controlled reaction conditions. Alpha- and gamma-MnO2 nanowires and nanorods were also prepared on the basis of previous literature. The as-synthesized samples were characterized by instrumental analyses such as XRD, SEM, TEM, and HRTEM. Furthermore, the obtained 1-D alpha- and gamma-MnO2 nanostructures were found to exhibit favorable discharge performance in both primary alkaline Zn-MnO2 cells and rechargeable Li-MnO2 cells, showing their potential applications in high-energy batteries.

We demonstrated in this paper the shape-controlled synthesis of ZnIn2S4, CuInS2, and CuInSe2 nano- and microstructures through a facile solution-based route. One-dimensional ZnIn2S4 nanotubes and nanoribbons were synthesized by a solvothermal method with pyridine as the solvent, while ZnIn2S4 solid or hollow microspheres were hydrothermally prepared in the presence of a surfactant such as cetyltrimethylammonium bromide (CTAB) or poly(ethylene glycol) (PEG). The mechanisms related to the phase formation and morphology control of ZnIn2S4 are proposed and discussed. The UV-vis absorption spectra show that the as-prepared nano- and micromaterials have strong absorption in a wide range from UV to visible light and that their band gaps are somewhat relevant to the size and morphology. The photoluminescence measurements of the ZnIn2S4 microspheres at room temperature reveal intense excitation at approximately 575 nm and red emission at approximately 784 nm. Furthermore, CuInS2 and CuInSe2 with different morphologies such as spheres, platelets, rods, and fishbone-like shapes were also obtained by similar hydrothermal and solvothermal synthesis.

No abstract

High‐power alkaline Zn–MnO2 batteries with superior discharge performance have been constructed using γ‐MnO2 nanowires/nanotubes (see Figure) and electrolytic zinc powder as the cathode and anode active materials, respectively. The improvement in discharge performance over commercial batteries is believed to be derived from the lower inner resistance of the batteries and the high utilization efficiency of the active materials.

We demonstrate computationally that two-dimensional polyphenylene is a typical semiconductor with a wide band gap, and the porous structure endows polyphenylene remarkably high selectivity for H(2) permeability relative to CO(2), CO and CH(4). This experimentally available porous graphene is expected to find applications in a hydrogen energy society.

The structural and electronic properties of graphane nanoribbons, i.e., completely hydrogenated graphene nanoribbons, were investigated by means of density functional theory computations. Because all the carbon atoms are sp 3 -hybridized and saturated with hydrogen atoms, graphane nanoribbons present completely different electronic properties compared with graphene nanoribbons. Independent of the chirality, graphane nanoribbons are always wide-band-gap semiconductors. Graphane nanoribbons have favorable formation energies, and can be realized by hydrogenating graphene nanoribbons or cutting experimentally available graphanes. These one-dimensional hydrocarbons will find their potential applications to nanotechnology after further band structure tuning.