Highly anisotropic and robust excitons in monolayer black phosphorus

Xiaomu Wang, Aaron M. Jones, Kyle L. Seyler, Vy Tran, Yichen Jia, Huan Zhao, Han Wang, Li Yang, Xiaodong Xu, Fengnian Xia

Research output: Contribution to journalArticlepeer-review

1262 Scopus citations

Abstract

Semi-metallic graphene and semiconducting monolayer transition-metal dichalcogenides are the most intensively studied two-dimensional materials of recent years. 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. 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 2.2eV, from which we estimate an exciton binding energy of ∼ 0.9eV, 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.

Original languageEnglish
Pages (from-to)517-521
Number of pages5
JournalNature Nanotechnology
Volume10
Issue number6
DOIs
StatePublished - Jun 6 2015
Externally publishedYes

Funding

The UW facility is partially supported by the State of Washington through the University of Washington Clean Energy Institute. V.T. and L.Y. are supported by the National Science Foundation (DMR-1207141). The authors acknowledge Mildred Dresselhaus at Massachusetts Institute of Technology for helpful comments during the preparation of the manuscript. This work was mainly supported by the Office of Naval Research (N00014-14-1-0565). M.J., K.S. and X.X. are supported by the Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division (DE-SC0008145 and DE-SC0012509). H.Z. and H.W. are supported by Army Research Laboratory (W911NF-14-2-0113). The use of facilities in Yale was supported by Yale Institute for Nanoscience and Quantum Engineering (YINQE) and the National Science Foundation (MRSEC DMR-1119826).

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