Theory of Graphene Raman Spectroscopy
Eric J. Heller, Yuan Yang, Lucas Kocia, Wei Chen, Shiang Fang, Mario, Borunda, Efthimios Kaxiras

TL;DR
This paper extends the classical Kramers-Heisenberg-Dirac Raman scattering theory to crystalline graphene, providing a comprehensive explanation for its Raman spectrum and introducing new mechanisms like transition sliding.
Contribution
It is the first to adapt KHD theory to graphene, contrasting it with the double resonance model, and introduces the transition sliding mechanism for phonon production.
Findings
KHD theory explains all features of graphene's Raman spectrum.
Transition sliding accounts for the brightness of the 2D mode.
Doping experiments support the sliding mechanism.
Abstract
Raman spectroscopy plays a key role in studies of graphene and related carbon systems. Graphene is perhaps the most promising material of recent times for many novel applications, including electronics. In this paper, the traditional and well established Kramers-Heisenberg-Dirac (KHD) Raman scattering theory (1925-1927) is extended to crystalline graphene for the first time. It demands different phonon production mechanisms and phonon energies than does the popular "double resonance" Raman scattering model. The latter has never been compared to KHD. Within KHD, phonons are produced instantly along with electrons and holes, in what we term an electron-hole-phonon triplet, which does not suffer Pauli blocking. A new mechanism for double phonon production we name "transition sliding" explains the brightness of the 2D mode and other overtones, as a result of linear (Dirac cone) electron…
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Taxonomy
TopicsGraphene research and applications · Graphene and Nanomaterials Applications · Fullerene Chemistry and Applications
