Fugui Xu | Searcharxiv

arXiv2020

Experimental Observation of Strong Exciton Effects in Graphene Nanoribbons

Graphene nanoribbons (GNRs) with atomically precise width and edge structures are a promising class of nanomaterials for optoelectronics, thanks to their semiconducting nature and high mobility of charge carriers. Understanding the fundamental static optical properties and ultrafast dynamics of charge carrier generation in GNRs is essential for optoelectronic applications. Combining THz spectroscopy and theoretical calculations, we report a strong exciton effect with binding energy up to 700 meV in liquid-phase-dispersed GNRs with a width of 1.7 nm and an optical bandgap of 1.6 eV, illustrating the intrinsically strong Coulomb interactions between photogenerated electrons and holes. By tracking the exciton dynamics, we reveal an ultrafast formation of excitons in GNRs with a long lifetime over 100 ps. Our results not only reveal fundamental aspects of excitons in GNRs (gigantic binding energy and ultrafast exciton formation etc.), but also highlight promising properties of GNRs for optoelectronic devices.

cond-mat.mes-hall↗

arXiv2019

Multi-wavelength Raman Spectroscopy of Ultra-narrow Nanoribbons Made by Solution-mediated Bottom-up Approach

Here we present a combined experimental and theoretical study of graphene nanoribbons (GNRs), where detailed multi-wavelength Raman measurements are integrated by accurate ab initio simulations. Our study covers several ultra-narrow GNRs, obtained by means of solution-based bottom-up synthetic approach, allowing to rationalize the effect of edge morphology, position and type of functional groups as well as the length on the GNR Raman spectrum. We show that the low-energy region, especially in presence of bulky functional groups is populated by several modes, and a single radial breathing-like mode cannot be identified. In the Raman optical region, we find that, except for the fully-brominated case, all GNRs functionalized at the edges with different side groups show a characteristic dispersion of the D peak (8-22 cm-1/eV). This has been attributed to the internal degrees of freedom of these functional groups, which act as dispersion-activating defects. The G peak shows small to negligible dispersion in most of the cases, with larger values only in presence of poor control of the edges functionalization, exceeding the values reported for highly defected graphene. In conclusion, we have shown that the characteristic dispersion of the G and D peaks offer further insight on the GNR structure and functionalization, by making Raman spectroscopy an important tool for the characterization of GNRs.

cond-mat.mtrl-sci↗