posted on 2019-02-12, 00:00authored byWei Wu, Mayra Daniela Morales-Acosta, Yongqiang Wang, Michael Thompson Pettes
Isotopes of an element
have the same electron number but differ
in neutron number and atomic mass. However, due to the thickness-dependent
properties in MX<sub>2</sub> (M = Mo, W; X = S, Se, Te) transition
metal dichalcogenides (TMDs), the isotopic effect in atomically thin
TMDs still remains unclear especially for phonon-assisted indirect
excitonic transitions. Here, we report the first observation of the
isotope effect on the electronic and vibrational properties of a TMD
material, using naturally abundant <sup>NA</sup>W<sup>NA</sup>Se<sub>2</sub> and isotopically pure <sup>186</sup>W<sup>80</sup>Se<sub>2</sub> bilayer single crystals over a temperature range of
4.4–300 K. We demonstrate a higher optical band gap energy
in <sup>186</sup>W<sup>80</sup>Se<sub>2</sub> than in <sup>NA</sup>W<sup>NA</sup>Se<sub>2</sub> (3.9 ± 0.7 meV from 4.41 to 300
K), which is surprising as isotopes are neutral impurities. Phonon
energies decrease in the isotopically pure crystal due to the atomic
mass dependence of harmonic oscillations, with correspondingly longer
E<sub>2g</sub> and A<sup>2</sup><sub>1g</sub> phonon lifetimes than
in the naturally abundant sample. The change in electronic band gap
renormalization energy is postulated as being the dominant mechanism
responsible for the change in optical emission spectra.