Searcharxiv⌕ Search

arXiv subjects

Luiz G. Cançado

Publications and source records attributed to Luiz G. Cançado.

3 recordsLinked to original sources

Theory for tip-enhanced Raman spectroscopy of two-dimensional materials including out-of-plane Raman response

Tip-Enhanced Raman Spectroscopy (TERS) can be used to make nanoscale spatial measurements of 2D materials, such as graphene and transition metal dichalcogenides (TMDs). The TERS theory introduced in [L. Cançado et al., Phys. Rev. X 4, 031054 (2014)], however, was tailored for graphene, whose out-of-plane Raman response is neglected. In the present work, we include the out-of-plane response in the TERS theory. In doing so, we provide an exact analytical expression for the field propagation between the tip and the sample, and show that the contribution to the TERS signal that scatters first at the sample, then at the tip (sample-tip, or TS) is important only when the out-of-plane response is significant. We extensively study the variation of TERS experimental measurements when varying physical parameters of the system, like the tip radius, the out-of-plane response, the TERS coherence length, and others. It becomes evident that the TERS enhancement is very sensitive to the out-of-plane Raman response of the phonon mode, while normalized tip-approach measurements are more sensitive to the coherence length, and we show that the medium refractive index leads to an effective tip enhancement factor $f_e$. Our results lead to the conclusion that, in general, a strong TERS enhancement is a necessary condition for investigating the physics discussed here, which here means surveying the difference in TERS signals between different Raman modes. We use our model to analyze some graphene TERS experiments, showing that they are consistent with a negligible out-of-plane Raman response and a nonzero TERS coherence length in the fitting.

physics.optics↗

Lattice dynamics localization in low-angle twisted bilayer graphene

A low twist angle between the two stacked crystal networks in bilayer graphene enables self-organized lattice reconstruction with the formation of a periodic domain. This superlattice modulates the vibrational and electronic structures, imposing new rules for electron-phonon coupling and the eventual observation of strong correlation and superconductivity. Direct optical images of the crystal superlattice in reconstructed twisted bilayer graphene are reported here, generated by the inelastic scattering of light in a nano-Raman spectroscope. The observation of the crystallographic structure with visible light is made possible due to lattice dynamics localization, the images resembling spectral variations caused by the presence of strain solitons and topological points. The results are rationalized by a nearly-free-phonon model and electronic calculations that highlight the relevance of solitons and topological points, particularly pronounced for structures with small twist angles. We anticipate our discovery to play a role in understanding Jahn-Teller effects and electronic Cooper pairing, among many other important phonon-related effects, and it may be useful for characterizing devices in the most prominent platform for the field of twistronics.

cond-mat.mes-hall↗

Evidence for a pressure-induced phase transition of few-layer graphene to 2D diamond

We unveil the diamondization mechanism of few-layer graphene compressed in the presence of water, providing robust evidence for the pressure-induced formation of 2D diamond. High-pressure Raman spectroscopy provides evidence of a phase transition occurring in the range of 4-7 GPa for 5-layer graphene and graphite. The pressure-induced phase is partially transparent and indents the silicon substrate. Our combined theoretical and experimental results indicate a gradual top-bottom diamondization mechanism, consistent with the formation of diamondene, a 2D ferromagnetic semiconductor. High-pressure x-ray diffraction on graphene indicates the formation of hexagonal diamond, consistent with the bulk limit of eclipsed-conformed diamondene.

cond-mat.mtrl-sci↗