First-principles calculations are carried out to investigate the hydrogen separation characteristics of two-dimensional carbon allotropes consisting of sp-and sp 2 -hybridized carbon atoms, i.e., graphyne, graphdiyne, and rhombic-graphyne. The selectivities for H 2 over several gas molecules, including CO, N 2 , and CH 4 , are found to be sensitive to the pore sizes and shapes. The penetration barriers generally decrease exponentially with the pore sizes. Our results reveal that graphyne with small pores is unsuitable for the purpose of hydrogen separation. Graphdiyne, with larger pores, exhibits a high selectivity (10 9 ) for hydrogen over large gas molecules such as CH 4 , but a relatively low selectivity (10 3 ) over small molecules such as CO and N 2 . The large differences in diffusion barriers for molecules penetration through a rhombic-graphyne monolayer, which possesses pore size in between that of graphyne and graphdiyne, lead to a high selectivity (>10 16 ) for hydrogen separation from the others. The results suggest that the abundant pores of different sizes in these carbon allotropes make them ideal molecular sieves for gas separation applications directed toward different separation needs and objectives.

We have carried out first-principles calculations to explore the energetics and dynamics of Li in graphdiyne monolayers. The porous structure of graphdiyne enables both in-plane and out-plane diffusion of Li ions with moderate barriers, 0.35–0.52 eV. A unique Li occupation pattern named as a triangular pattern is identified, with Li atoms occupying three symmetric sites in the triangular-like pores. Based on this occupation pattern, the Li storage capacity of single-layer graphdiyne can be as high as LiC3, which is twice the capacity of commonly used graphite (LiC6). With high Li mobility and high storage capacity, this experimentally available porous carbon material is expected to find applications in efficient lithium storage.

The geometries, stabilities, and electronic properties of Bn and AlBn clusters, up to n=12, have been systematically investigated by using the density-functional approach. The results of Bn clusters are in good agreement with previous conclusions. When the Al atom is doped in Bn clusters, the lowest-energy structures of the AlBn clusters favor two-dimensional and can be obtained by adding one Al atom on the peripheral site of the stable Bn when n

The catalytic behavior of transition metals (Sc to Zn) combined in polymeric phthalocyanine (Pc) is investigated systematically by using first-principles calculations. The results indicate that CoPc exhibits the highest catalytic activity for CO oxidation at room temperature with low energy barriers. By exploring the two well-established mechanisms for CO oxidation with O2 , namely, the Langmuir-Hinshelwood (LH) and the Eley-Rideal (ER) mechanisms, it is found that the first step of CO oxidation catalyzed by CoPc is the LH mechanism (CO + O2 → CO2 + O) with energy barrier as low as 0.65 eV. The second step proceeds via both ER and LH mechanisms (CO + O → CO2 ) with small energy barriers of 0.10 and 0.12 eV, respectively. The electronic resonance among Co-3d, CO-2π*, and O2 -2π* orbitals is responsible for the high activity of CoPc. These results have significant implications for a novel avenue to fabricate organometallic sheet nanocatalysts for CO oxidation with low cost and high activity.

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