it has been challenging to adequately investigate the properties of nanosystems with radical nature using conventional electronic structure methods. We address this challenge by calculating the electronic properties of linear carbon chains (l-cc[n]) and cyclic carbon chains (c-cc[n]) with n = 10-100 carbon atoms, using thermally-assisted-occupation density functional theory (TAO-DFT). For all the cases investigated, l-cc[n]/c-cc[n] are ground-state singlets, and c-cc[n] are energetically more stable than l-cc[n]. the electronic properties of l-cc[n]/c-cc[n] reveal certain oscillation patterns for smaller n, followed by monotonic changes for larger n. For the smaller carbon chains, odd-numbered l-cc[n] are more stable than the adjacent even-numbered ones; c-cc[4m + 2]/c-CC[4m] are more/less stable than the adjacent odd-numbered ones, where m are positive integers. As n increases, l-cc[n]/c-cc[n] possess increasing polyradical nature in their ground states, where the active orbitals are delocalized over the entire length of l-cc[n] or the whole circumference of c-cc[n]. Carbon is the most versatile element in forming various structures. In bulk phase, graphite and diamond, which are well-known materials, have been used for centuries. In nanoforms, fullerenes and graphene have been studied in detail for decades. In general, nanostructures can be classified into three categories: zero-dimensional (0D), one-dimensional (1D), and two-dimensional (2D) nanomaterials. Carbon forms all these nanostructures with unique shapes and properties. Over the past few decades, carbon nanomaterials have been widely studied, and applied in diverse industries 1-3. A number of carbon nanostructures have been synthesized and applied in different fields. The 0D carbon nanomaterials include clusters, quantum dots, nanoflakes, and buckyballs 3. Among them, the C 60 fullerene molecule (containing 12 pentagons and 20 hexagons), where the carbon atoms are sp 2-sp 3-hybridized, has been a popular carbon nanomaterial 1. The discovery of C 60 has led to the flourishment of carbon nanomaterials in various ways. Graphite is a bulk layered material, where the sp 2-hybridized carbon atoms in each layer are arranged in a hexagonal lattice. The 2D carbon nanomaterial, graphene, can be obtained by mechanically exfoliating a single layer of carbon atoms from graphite 2. Thus, graphene, which is a perfect arrangement of hexagons made up of sp 2-hybridized carbon atoms in a 2D planar surface, can be the thinnest (i.e., single-atom-thick) material synthesized ever. Graphene is a zero-gap semiconductor or semimetal with massless Dirac fermions with linear dispersion at low energy. Because of the Dirac-cone feature, graphene has huge potential in electronics applications 2. The discovery of graphene has also led to the discovery of other 2D materials. Besides, if a graphene sheet can be rolled up to form a seamless cylinder, one obtains a carbon nanotube (CNT), which belongs to the class of 1D nanostructures. Note that CNTs were first observed by Iijima in 19...

Due to the presence of strong static correlation effects and noncovalent interactions, accurate prediction of the electronic and hydrogen storage properties of Li-adsorbed acenes with n linearly fused benzene rings (n = 3–8) has been very challenging for conventional electronic structure methods. To meet the challenge, we study these properties using our recently developed thermally-assisted-occupation density functional theory (TAO-DFT) with dispersion corrections. In contrast to pure acenes, the binding energies of H2 molecules on Li-adsorbed acenes are in the ideal binding energy range (about 20 to 40 kJ/mol per H2). Besides, the H2 gravimetric storage capacities of Li-adsorbed acenes are in the range of 9.9 to 10.7 wt%, satisfying the United States Department of Energy (USDOE) ultimate target of 7.5 wt%. On the basis of our results, Li-adsorbed acenes can be high-capacity hydrogen storage materials for reversible hydrogen uptake and release at ambient conditions.

No abstract

It has been extremely difficult for conventional computational approaches to reliably predict the properties of multi-reference systems (i.e., systems possessing radical character) at the nanoscale. To resolve this, we employ thermally-assisted-occupation density functional theory (TAO-DFT) to predict the electronic and hydrogen storage properties of Li-terminated linear boron chains (Li2Bn), with n boron atoms (n = 6, 8, …, and 16). From our TAO-DFT results, Li2Bn, which possess radical character, can bind up to 4 H2 molecules per Li, with the binding energies in the desirable regime (between 20 and 40 kJ/mol per H2). The hydrogen gravimetric storage capacities of Li2Bn range from 7.9 to 17.0 wt%, achieving the ultimate goal of the United States Department of Energy. Accordingly, Li2Bn could be promising media for storing and releasing H2 at temperatures much higher than the boiling point of liquid nitrogen.

Accurate prediction of the electronic and hydrogen storage properties of linear carbon chains (Cn) and Li-terminated linear carbon chains (Li2Cn), with n carbon atoms (n = 5–10), has been very challenging for traditional electronic structure methods, due to the presence of strong static correlation effects. To meet the challenge, we study these properties using our newly developed thermally-assisted-occupation density functional theory (TAO-DFT), a very efficient electronic structure method for the study of large systems with strong static correlation effects. Owing to the alteration of the reactivity of Cn and Li2Cn with n, odd-even oscillations in their electronic properties are found. In contrast to Cn, the binding energies of H2 molecules on Li2Cn are in (or close to) the ideal binding energy range (about 20 to 40 kJ/mol per H2). In addition, the H2 gravimetric storage capacities of Li2Cn are in the range of 10.7 to 17.9 wt%, satisfying the United States Department of Energy (USDOE) ultimate target of 7.5 wt%. On the basis of our results, Li2Cn can be high-capacity hydrogen storage materials that can uptake and release hydrogen at temperatures well above the easily achieved temperature of liquid nitrogen.

No abstract

No abstract

It remains rather difficult for traditional computational methods to reliably predict the properties of nanosystems, especially for those possessing pronounced radical character. Accordingly, in this work, we adopt the recently formulated thermally-assisted-occupation density functional theory (TAO-DFT) to study two-atom-wide linear boron nanoribbons l -BNR[2, n ] and two-atom-wide cyclic boron nanoribbons c -BNR[2, n ], which exhibit polyradical character when the n value (i.e., the number of boron atoms along the length of l -BNR[2, n ] or the circumference of c -BNR[2, n ]) is considerably large. We calculate various electronic properties associated with l -BNR[2, n ] and c -BNR[2, n ], with n ranging from 6 to 100. Our results show that l -BNR[2, n ] and c -BNR[2, n ] have singlet ground states for all the n values examined. The electronic properties of c -BNR[2, n ] exhibit more pronounced oscillatory patterns than those of l -BNR[2, n ] when n is small, and converge to the respective properties of l -BNR[2, n ] when n is sufficiently large. The larger the n values, the stronger the static correlation effects that originate from the polyradical nature of these ribbons. Besides, the active orbitals are found to be delocalized along the length of l -BNR[2, n ] or the c ircumference of c -BNR[2, n ]. The analysis of the size-dependent electronic properties indicates that l -BNR[2, n ] and c -BNR[2, n ] can be promising for nanoelectronic devices.