Ni-doped MoS2 has useful
tribological, optoelectronic,
and catalytic properties. Experiment and theory on doped MoS2 have focused on monolayers or finite particles: theoretical studies
of bulk Ni-doped MoS2 are lacking and the mechanisms by
which Ni alters bulk properties are largely unsettled. We use density
functional theory calculations to determine the structure, mechanical
properties, electronic properties, and formation energies of bulk
Ni-doped 2H-MoS2 as a function of doping concentration.
We find four metastable structures: Mo or S substitution and tetrahedral
(t-) or octahedral (o-) intercalation. We compute phase diagrams as
a function of chemical potential to guide experimental synthesis.
Convex hull analysis shows that t-intercalation (favored over o-intercalation,
with doping formation energy ∼10 meV per Ni) is stable against
phase segregation and other compounds containing Ni, Mo, and S. Intercalation
forms strong interlayer covalent bonds and does not increase the c-parameter. Ni-doping creates new states in the electronic
density of states in MoS2 and shifts the Fermi level. We
calculate infrared and Raman spectra and find new peaks and shifts
in existing peaks that are unique to each dopant site, and therefore
may be used to identify the site experimentally, which has thus far
been challenging.
We present results of atomic-force-microscopy-based friction measurements on Re-doped molybdenum disulfide (MoS2). In stark contrast to the widespread observation of decreasing friction with increasing number of layers on two-dimensional (2D) materials, friction on Re-doped MoS2 exhibits an anomalous, i.e., inverse dependence on the number of layers. Raman spectroscopy measurements combined with ab initio calculations reveal signatures of Re intercalation. Calculations suggest an increase in out-of-plane stiffness that inversely correlates with the number of layers as the physical mechanism behind this remarkable observation, revealing a distinctive regime of puckering for 2D materials.
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