A molecular simulation analysis of producing monatomic carbon chains by stretching ultranarrow graphene nanoribbons
Zenan Qi, Fengpeng Zhao, Xiaozhou Zhou, Zehui Sun, Harold S Park and, Hengan Wu

TL;DR
This study uses atomistic simulations to explore how ultranarrow graphene nanoribbons can be stretched to form stable monatomic carbon chains, revealing chirality and width-dependent deformation mechanisms with potential nanoelectronic applications.
Contribution
It provides new insights into the formation processes, deformation mechanisms, and stability of monatomic carbon chains from ultranarrow GNRs, highlighting the influence of chirality and width.
Findings
Stable MACCs with >100% fracture strain can be formed.
Deformation processes depend strongly on GNR chirality.
Ultranarrow GNRs facilitate full MACC formation.
Abstract
Atomistic simulations were utilized to develop fundamental insights regarding the elongation process starting from ultranarrow graphene nanoribbons (GNRs) and resulting in monatomic carbon chains (MACCs). There are three key findings. First, we demonstrate that complete, elongated, and stable MACCs with fracture strains exceeding 100% can be formed from both ultranarrow armchair and zigzag GNRs. Second, we demonstrate that the deformation processes leading to the MACCs have strong chirality dependence. Specifically, armchair GNRs first form DNA-like chains, then develop into monatomic chains by passing through an intermediate configuration in which monatomic chain sections are separated by two-atom attachments. In contrast, zigzag GNRs form rope-ladder-like chains through a process in which the carbon hexagons are first elongated into rectangles; these rectangles eventually coalesce…
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