Graphullerite: A Thermally Conductive and Remarkably Ductile Allotrope of Polymerized Carbon.

The understanding of the fundamental relationships between chemical bonding and material properties, especially for carbon allotropes with diverse orbital hybridizations, is significant from both scientific and applicative standpoints. Here, we elucidate the influence of the intermolecular covalent bond configuration on the mechanical and thermal properties of polymerized fullerenes by performing systematic atomistic simulations on graphullerite, a newly synthesized crystalline polymer of C with a hexagonal lattice similar to that of graphene. Specifically, we show that the polymerization of C molecules into two-dimensional sheets (and three-dimensional layered structures) offers tunable control over their mechanical and thermal properties via the replacement of weak intermolecular van der Waals interactions between the fullerene molecules with strong sp covalent bonds.

A few-layer covalent network of fullerenes.

The two natural allotropes of carbon, diamond and graphite, are extended networks of sp-hybridized and sp-hybridized atoms, respectively. By mixing different hybridizations and geometries of carbon, one could conceptually construct countless synthetic allotropes. Here we introduce graphullerene, a two-dimensional crystalline polymer of C that bridges the gulf between molecular and extended carbon materials.

Pore Size Dictates Anisotropic Thermal Conductivity of Two-Dimensional Covalent Organic Frameworks with Adsorbed Gases.

Two-dimensional covalent organic frameworks (2D COFs) are a class of modular polymeric crystals with high porosities and large surface areas, which position them as ideal candidates for applications in gas storage and separation technologies. In this work, we study the influence of pore geometry on the anisotropic heat transfer mechanisms in 2D COFs through systematic atomistic simulations. More specifically, by studying COFs with varying pore sizes and gas densities, we demonstrate that the cross-plane thermal conductivity along the direction of the laminar pores can either be decreased due to solid-gas scattering (for COFs with relatively smaller pores that are ≲2 nm) or increased due to additional heat transfer pathways introduced by the gas adsorbates (for COFs with relatively larger pores).

Supramolecular Interactions Lead to Remarkably High Thermal Conductivities in Interpenetrated Two-Dimensional Porous Crystals.

The design of innovative porous crystals with high porosities and large surface areas has garnered a great deal of attention over the past few decades due to their remarkable potential for a variety of applications. However, heat dissipation is key to realizing their potential. We use systematic atomistic simulations to reveal that interpenetrated porous crystals formed from two-dimensional (2D) frameworks possess remarkable thermal conductivities at high porosities in comparison to their three-dimensional (3D) single framework and interpenetrated 3D framework counterparts.