Abstract
Ferroelectricity, the electrostatic counterpart to ferromagnetism, has long been thought to be incompatible with metallicity due to screening of electric dipoles and external electric fields by itinerant charges. Recent measurements, however, demonstrated signatures of ferroelectric switching in the electrical conductance of bilayers and trilayers of WTe2, a semimetallic transition metal dichalcogenide with broken inversion symmetry. An especially promising aspect of this system is that the density of electrons and holes can be continuously tuned by an external gate voltage. This degree of freedom enables measurement of the spontaneous polarization as free carriers are added to the system. Here we employ capacitive sensing in dual-gated mesoscopic devices of bilayer WTe2 to directly measure the spontaneous polarization in the metallic state and quantify the effect of free carriers on the polarization in the conduction and valence bands, separately. We compare our results to a low-energy model for the electronic bands and identify the layer-polarized states that contribute to transport and polarization simultaneously. Bilayer WTe2 is thus shown to be a fully tunable ferroelectric metal and an ideal platform for exploring polar ordering, ferroelectric transitions, and applications in the presence of free carriers.
Original language | English |
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Article number | 5298 |
Journal | Nature Communications |
Volume | 12 |
Issue number | 1 |
DOIs | |
State | Published - Dec 1 2021 |
Funding
We thank Qiong Ma, Kenji Yasuda, Felix Lüpke, Dacen Waters, and Evan Telford for fruitful discussions. B.M.H., S.C.d.l.B., and Q.C. were supported by the Department of Energy under the Early Career award program (DE-SC0018115) for all aspects of this project. Yang Gao and D.X. are supported by the Department of Energy, Basic Energy Sciences, Grant No. DE-SC0012509. J.Y. and D.G.M. acknowledge support from the U.S. Department of Energy (U.S.-DOE), Office of Science - Basic Energy Sciences (BES), Materials Sciences and Engineering Division. W.Z. acknowledges support from the National Key Research and Development Program of China (2019YFA0210004).