4.8 Article

Nanoimaging of the Edge-Dependent Optical Polarization Anisotropy of Black Phosphorus

Journal

NANO LETTERS
Volume 22, Issue 8, Pages 3180-3186

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.1c03849

Keywords

black phosphorus; 2D materials; anisotropic material; edge electronic states

Funding

  1. Office of Basic Energy Sciences, U.S. Department of Energy [DE-SC0021950]
  2. University of Chicago Materials Research Science and Engineering Center - National Science Foundation [DMR-2011854, DMR-1420709]
  3. National Science Foundation [DMR-2011854]
  4. MRSEC [DMR-2011854, DMR1420709]
  5. University of Chicago
  6. Neubauer Family Assistant Professors Program
  7. Office of Science of the U.S. Department of Energy [DE-AC0500OR22725]
  8. U.S. Department of Energy (DOE) [DE-SC0021950] Funding Source: U.S. Department of Energy (DOE)

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This study used polarization-dependent photoemission electron microscopy to visualize the anisotropic optical absorption of black phosphorus (BP) flakes and found different characteristics of optical absorption at the edges compared to the interior. This phenomenon is caused by changes in the charge distribution and transition dipole moments of edge electronic states.
The electronic structure and functionality of 2D materials is highly sensitive to structural morphology, not only opening the possibility for manipulating material properties but also making predictable and reproducible functionality challenging. Black phosphorus (BP), a corrugated orthorhombic 2D material, has in-plane optical absorption anisotropy critical for applications, such as directional photonics, plasmonics, and waveguides. Here, we use polarization-dependent photoemission electron microscopy to visualize the anisotropic optical absorption of BP with 54 nm spatial resolution. We find the edges of BP flakes have a shift in their optical polarization anisotropy from the flake interior due to the 1D confinement and symmetry reduction at flake edges that alter the electronic charge distributions and transition dipole moments of edge electronic states, confirmed with first-principles calculations. These results uncover previously hidden modification of the polarization-dependent absorbance at the edges of BP, highlighting the opportunity for selective excitation of edge states of 2D materials with polarized light.

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