4.8 Article

Highly anisotropic and robust excitons in monolayer black phosphorus

Journal

NATURE NANOTECHNOLOGY
Volume 10, Issue 6, Pages 517-521

Publisher

NATURE RESEARCH
DOI: 10.1038/NNANO.2015.71

Keywords

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Funding

  1. Office of Naval Research [N00014-14-1-0565]
  2. Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division [DE-SC0008145, DE-SC0012509]
  3. Army Research Laboratory [W911NF-14-2-0113]
  4. Yale Institute for Nanoscience and Quantum Engineering (YINQE)
  5. National Science Foundation [MRSEC DMR-1119826, DMR-1207141]
  6. State of Washington through the University of Washington Clean Energy Institute
  7. Direct For Mathematical & Physical Scien
  8. Division Of Materials Research [1207141] Funding Source: National Science Foundation
  9. Division Of Materials Research
  10. Direct For Mathematical & Physical Scien [GRANTS:13743485] Funding Source: National Science Foundation

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Semi-metallic graphene and semiconducting monolayer transition- metal dichalcogenides are the most intensively studied two-dimensional materials of recent years(1,2). Lately, black phosphorus has emerged as a promising new two-dimensional material due to its widely tunable and direct bandgap, high carrier mobility and remarkable in-plane anisotropic electrical, optical and phonon properties(3-9). However, current progress is primarily limited to its thin-film form. Here, we reveal highly anisotropic and strongly bound excitons in monolayer black phosphorus using polarization-resolved photoluminescence measurements at room temperature. We show that, regardless of the excitation laser polarization, the emitted light from the monolayer is linearly polarized along the light effective mass direction and centres around 1.3 eV, a clear signature of emission from highly anisotropic bright excitons. Moreover, photoluminescence excitation spectroscopy suggests a quasiparticle bandgap of 2.2 eV, from which we estimate an exciton binding energy of similar to 0.9 eV, consistent with theoretical results based on first principles. The experimental observation of highly anisotropic, bright excitons with large binding energy not only opens avenues for the future explorations of many-electron physics in this unusual two-dimensional material, but also suggests its promising future in optoelectronic devices.

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