The electromagnetic field enhancement mechanisms leading to surface-enhanced Raman scattering
(SERS) of R6G molecules near Ti3C2Tx MXene flakes of different shapes and sizes are analyzed theoretically. In COMSOL simulations for the enhancement factor (EF) of SERS, the dye molecule is modeled
as a small sphere with polarizability spectrum based on experimental data. It is demonstrated for the
first time, that in the wavelength range 500 nm − 1000 nm the enhancement of Raman signal is largely
conditioned by quadrupole surface plasmon (QSP) oscillations that induce strong polarization of MXene substrate. We show that in 
vis-NIR spectral range quadrupole SP resonances, strengthened due to
interband transitions (IBT) provide EF values of the order of 105 - 107 in agreement with experimental
data. The weak sensitivity of the EF to the shape and size of MXene nanoparticles (NPs) is interpreted
as a consequence of the low dependence of the absorption cross-section of QSP oscillations and IBT
on the geometry of the flakes. This reveals a new feature - the independence of EF on the geometry of
MXene substrates, allowing to avoid the monitoring of the shape and size of flakes during their synthe-
sis. Thus, MXene flakes can be advantageous for easy manufacturing of universal substrates for SERS
applications. The electromagnetic SERS enhancement is determined by the “lightning rod” and “hot-spot” effects due to partial overlapping of absorption spectrum of the R6G molecule with these MXene resonances.