Using first-principles calculations, we investigate electromechanical properties of two-dimensional (2D) hexagonal and pentagonal materials as a function of electron and hole dopings, in which 2D materials including graphene, chair-like graphane, table-like graphane, penta-graphene (PG), hydrogenated penta-graphene (HPG), and penta-CN2 are considered. We find that the actuation responses such as actuation strain, stress generated, and work area-density per cycle of the 2D materials in the case of hole doping are substantially larger than those of electron doping. Moreover, the electromechanical properties of the 2D materials can be improved by hydrogenation. In particular, the actuation strain and work area-density per cycle of graphane and HPG are much larger than those of graphene and PG for hole doping, respectively. Interestingly, both the 2D hexagonal and pentagonal materials show an asymmetric dependence of theoretical strength (a maximum value of the stress that the materials can achieve by applying the strain) on the electron and hole dopings. These results provide an important insight into the electromechanical properties of the 2D hexagonal and pentagonal materials, which are useful for artificial muscle applications.
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ACS Omega
December 2024
Electronic Structure and Atomistic Dynamics Interdisciplinary Group (GEEDAI), Center for Natural and Human Sciences (CCNH), Federal University of ABC (UFABC), Avenida dos Estados 5001, 09210-580 Santo Andre, Sao Paulo, Brazil.
Tetra-Penta-Deca-Hexa graphene (TPDH) is a new two-dimensional (2D) carbon allotrope with attractive electronic and mechanical properties. It is composed of tetragonal, pentagonal, decagonal and hexagonal carbon rings. When TPDH graphene is sliced into quasi-one-dimensional (1D) structures such as nanoribbons, it exhibits a range of behaviors, from semimetallic to semiconducting.
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December 2024
School of Civil Engineering, University of Sydney, Sydney, NSW 2006, Australia.
Disordered hyperuniform materials are increasingly drawing attention due to their unique physical properties, associated with global isotropy and locally broken orientational symmetry, that set them apart from traditional crystalline materials. Using a dynamic space-partitioning process, we generate disordered hyperuniform cellular structures where distinct patterns of pentagonal and heptagonal topological defects emerge within hexagonal domains. The microscopic defect dynamics are guided by local topological transitions, commonly observed in viscoelastic systems.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Incorporation of heteroatoms and/or non-hexagonal rings into polycyclic aromatic hydrocarbons (PAHs) can alter their intrinsic structures and physical properties. However, it is challenging to construct PAHs featuring boron/carbon composition and non-hexagonal combination. Herein, we disclose the selective synthesis of spiro-type and pentagon/heptagon-containing boron-doped polycyclic π-systems by the Scholl reaction.
View Article and Find Full Text PDFMaterials (Basel)
November 2024
School of Physics, State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China.
Angew Chem Int Ed Engl
November 2024
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, 100190, Beijing, P. R. China.
The transfer-free character of graphene growth on Silicon Carbide (SiC) makes it compatible with state-of-the-art Si semiconductor technologies for directly fabricating high-end electronics. Although significant progress has been achieved in epitaxial growth of graphene on SiC recently, the underlying nucleation mechanism remains elusive. Here, we present a theoretical study to elucidate graphene near-equilibrium nucleation on Si-terminated hexagonal-SiC(0001) surface.
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