A Universal Method to Transform Aromatic Hydrocarbon Molecules into Confined Carbyne inside Single-Walled Carbon Nanotubes

TL;DR

This paper introduces a universal low-temperature method to synthesize confined carbyne inside single-walled carbon nanotubes using aromatic hydrocarbons, enabling property tuning and extending synthesis to various nanostructures.

Contribution

It presents a novel, versatile approach for converting aromatic hydrocarbons into confined carbyne inside SWCNTs, overcoming previous limitations to multi-walled CNTs.

Findings

Effective aromatic precursors identified for CC formation.

Optimal SWCNT diameters are 0.9-1.3 nm for synthesis.

Resonance Raman confirms CC optical band gap at 2.353 eV.

Abstract

Carbyne, a sp1-hybridized allotrope of carbon, is a linear carbon chain with exceptional theoretically predicted properties that surpass those of sp2-hybridized graphene and carbon nanotubes (CNTs). However, the existence of carbyne has been debated due to its instability caused by Peierls distortion, which limits its practical development. The only successful synthesis of carbyne has been achieved inside CNTs, resulting in a form known as confined carbyne (CC). However, CC can only be synthesized inside multi-walled CNTs, limiting its property-tuning capabilities to the inner tubes of the CNTs. Here, we present a universal method for synthesizing CC inside single-walled carbon nanotubes (SWCNTs) with diameter of 0.9-1.3 nm. Aromatic hydrocarbon molecules are filled inside SWCNTs and subsequently transformed into CC under low-temperature annealing. A variety of aromatic hydrocarbon molecules are confirmed as effective precursors for formation of CC, with Raman frequencies centered around 1861 cm-1. Enriched (6,5) and (7,6) SWCNTs with diameters less than 0.8 nm are less effective than the SWCNTs with diameter of 0.9-1.3 nm for CC formation. Furthermore, resonance Raman spectroscopy reveals that optical band gap of the CC at 1861 cm-1 is 2.353 eV, which is consistent with the result obtained using a linear relationship between the Raman signal and optical band gap. This newly developed approach provides a versatile route for synthesizing CC from various precursor molecules inside diverse templates, which is not limited to SWCNTs but could extend to any templates with appropriate size, including molecular sieves, zeolites, boron nitride nanotubes, and metal-organic frameworks.