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Raman signature and phonon dispersion of atomically thin boron nitride

journal contribution
posted on 07.03.2017, 00:00 authored by Qiran CaiQiran Cai, D Scullion, Aleksey Falin, K Watanabe, T Taniguchi, Ying (Ian) ChenYing (Ian) Chen, E J G Santos, Luhua LiLuhua Li
Raman spectroscopy has become an essential technique to characterize and investigate graphene and many other two-dimensional materials. However, there is still a lack of consensus on the Raman signature and phonon dispersion of atomically thin boron nitride (BN), which has many unique properties distinct from graphene. Such a knowledge gap greatly affects the understanding of the basic physical and chemical properties of atomically thin BN as well as the use of Raman spectroscopy to study these nanomaterials. Here, we use both experiment and simulation to reveal the intrinsic Raman signature of monolayer and few-layer BN. We find experimentally that atomically thin BN without interaction with a substrate has a G band frequency similar to that of bulk hexagonal BN (hBN), but strain induced by the substrate can cause a pronounced Raman shift. This is in excellent agreement with our first-principles density functional theory (DFT) calculations at two levels of theory, including van der Waals dispersion forces (opt-vdW) and a fraction of the exact exchange from Hartree-Fock (HF) theory through the hybrid HSE06 functional. Both calculations demonstrate that the intrinsic E2g mode of BN does not depend sensibly on the number of layers. Our simulations also suggest the importance of the exact exchange mixing parameter in calculating the vibrational modes in BN, as it determines the fraction of HF exchange included in the DFT calculations.

History

Journal

Nanoscale

Volume

9

Issue

9

Pagination

3059 - 3067

Publisher

Royal Society of Chemistry

Location

Cambridge, Eng.

eISSN

2040-3372

Language

eng

Publication classification

C1 Refereed article in a scholarly journal

Copyright notice

2017, The Royal Society of Chemistry