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Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides
Published on: November 21, 2013
A new phosphorene allotrope: the assembly of phosphorene nanoribbons and chains
Congling Dai1, Xinyong Cai1, Yuxiang Ni1
1School of Physical Science and Technology, Key Laboratory of Advanced Technology of Materials, Ministry of Education of China, Southwest Jiaotong University, Chengdu 610031, China. hongyanw@swjtu.edu.cn.
Abstract:
Phosphorene allotrope monolayers such as blue and red phosphorus are being designed and synthesized to be used in the optoelectronics field due to their tunable bandgap and high mobility. Using the organic molecule self-assembly method similar to the synthesis of graphene allotropes, a novel phosphorene allotrope, P567 monolayer, with five-, six-, and seven-membered rings is designed through the assembly of black phosphorus chains and blue phosphorene nanoribbons. Ab initio molecular dynamics, phonon dispersion, and elastic constants demonstrate the dynamic, thermal, and mechanical stability of the P567 monolayer. Additionally, the first-principles calculations show that the P567 monolayer is an indirect bandgap semiconductor with moderate bandgap and high anisotropic mobility (4.47 × 103 cm2 V-1 s-1). Compared with black phosphorene, the suitable band edge position and higher optical absorption coefficient (105 cm-1) make the P567 monolayer more likely to be used as a photocatalytic hydrolysis material. The P567 monolayer is a viable candidate for use in innovative optoelectronic devices and the assembly method provides a rational approach to designing phosphorus allotropes with high photocatalytic efficiency.
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