Van der Waals heterostructures is a unique class of layered artificial solids that offers the possibility of manipulating their physical properties via controlled composition, order and relative rotation of adjacent atomic planes. Here we use atomic resolution transmission electron microscopy to reveal the lattice reconstruction in twisted MoS 2 and WS 2 bilayers. For 3R stacking, a tessellated pattern of mirror reflected triangular 3R domains emerges, separated by a network of partial dislocations for the twist angles θ < 2 •. The electronic properties of these 3R domains appear qualitatively different from 2H TMDs, featuring layer-polarized conduction band states caused by lack of both inversion and mirror symmetry. In contrast, for 2H stacking, stable 2H domains dominate, with nuclei of a second metastable phase. This appears as a kagome-like pattern at θ ∼ 1 • , transitioning at θ → 0 to a hexagonal array of screw dislocations separating large-area 2H domains. The tunneling measurements show that such reconstruction creates strong piezoelectric textures, opening a new avenue for engineering of 2D material properties.
The
localized surface plasmon resonance (LSPR) excitation in plasmonic
nanoparticles has been used to accelerate several catalytic transformations
under visible-light irradiation. In order to fully harness the potential
of plasmonic catalysis, multimetallic nanoparticles containing a plasmonic
and a catalytic component, where LSPR-excited energetic charge carriers
and the intrinsic catalytic active sites work synergistically, have
raised increased attention. Despite several exciting studies observing
rate enhancements, controlling reaction selectivity remains very challenging.
Here, by employing multimetallic nanoparticles combining Au, Ag, and
Pt in an Au@Ag@Pt core–shell and an Au@AgPt nanorattle architectures,
we demonstrate that reaction selectivity of a sequential reaction
can be controlled under visible light illumination. The control of
the reaction selectivity in plasmonic catalysis was demonstrated for
the hydrogenation of phenylacetylene as a model transformation. We
have found that the localized interaction between the triple bond
in phenylacetylene and the Pt nanoparticle surface enables selective
hydrogenation of the triple bond (relative to the double bond in styrene)
under visible light illumination. Atomistic calculations show that
the enhanced selectivity toward the partial hydrogenation product
is driven by distinct adsorption configurations and charge delocalization
of the reactant and the reaction intermediate at the catalyst surface.
We believe these results will contribute to the use of plasmonic catalysis
to drive and control a wealth of selective molecular transformations
under ecofriendly conditions and visible light illumination.
Through simultaneously enhancing the power factor by engineering the extra light band and enhancing phonon scatterings by introducing a high density of stacking faults, a record figure‐of‐merit over 2.0 is achieved in p‐type AgSbTe2−xSex alloys. Density functional theory calculations confirm the presence of the light valence band with large degeneracy in AgSbTe2, and that alloying with Se decreases the energy offset between the light valence band and the valence band maximum. Therefore, a significantly enhanced power factor is realized in p‐type AgSbTe2−xSex alloys. In addition, transmission electron microscopy studies indicate the appearance of stacking faults and grain boundaries, which together with grain boundaries and point defects significantly strengthen phonon scatterings, leading to an ultralow thermal conductivity. The synergetic strategy of simultaneously enhancing power factor and strengthening phonon scattering developed in this study opens up a robust pathway to tailor thermoelectric performance.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.