Valerie Hsieh

The "gold-tape" exfoliation technique can deterministically exfoliate macroscopic transition metal dichalcogenide (TMD) monolayers from bulk single crystals, overcoming limitations of the widely used "Scotch-tape" method, but concerns over the quality of the large-area monolayers remain. Here we introduce a critical step improving the gold-tape method by eliminating a previously unknown polymer residue layer on the TMD surface. The resulting pristine and millimeter-scale TMD monolayers exhibit defect density, charge carrier mobility, and excitonic properties intrinsic to the parent crystal. Imaging, transport, and spectroscopy on length scales spanning 6 orders of magnitude demonstrate the viability of gold-exfoliated TMD monolayers for the deterministic fabrication of high-performance van der Waals devices, including moiré interfaces.

Surface plasmon polaritons (SPPs) provide a window into the nano-optical, electrodynamic response of their host material and its dielectric environment. Graphene/α-RuCl₃ serves as an ideal model system for imaging SPPs since the large work function difference between these two layers facilitates charge transfer that hole dopes graphene with n ∼ 10¹³ cm^-2 free carriers. In this work, we study the emergent THz response of graphene/α-RuCl₃ heterostructures using our home-built cryogenic scanning near-field optical microscope. Using phase-resolved imaging, we clearly observe long wavelength, heavily damped THz SPPs in a series of variable-size graphene cavities. From this, we extract the plasmonic wavelength and scattering rate in the graphene/α-RuCl₃ heterostructures. We determine that the measured plasmon wavelength and electronic scattering rate match our heterostructures' theoretically predicted values. Our results demonstrate that shaping graphene into bespoke cavity structures enables observation and quantification of SPPs in heavily doped graphene that are largely not addressable with other experimental techniques. Moreover, the manifest lack of metallicity observed in the adjacent doped α-RuCl₃ layer provides significant constraints on the nature of the interfacial charge transfer in this 2D heterostructure.

Moiré superlattices in twisted two-dimensional materials have generated tremendous excitement as a platform for achieving quantum properties on demand. However, the moiré pattern is highly sensitive to the interlayer atomic registry, and current assembly techniques suffer from imprecise control of the average twist angle, spatial inhomogeneity in the local twist angle, and distortions caused by random strain. We manipulated the moiré patterns in hetero- and homobilayers through in-plane bending of monolayer ribbons, using the tip of an atomic force microscope. This technique achieves continuous variation of twist angles with improved twist-angle homogeneity and reduced random strain, resulting in moiré patterns with tunable wavelength and ultralow disorder. Our results may enable detailed studies of ultralow-disorder moiré systems and the realization of precise strain-engineered devices.

Twisted van der Waals multilayers are widely regarded as a rich platform to access novel electronic phases thanks to the multiple degrees of freedom available for controlling their electronic and chemical properties. Here, we propose that the stacking domains that form naturally due to the relative twist between successive layers act as an additional "knob" for controlling the behavior of these systems and report the emergence and engineering of stacking domain-dependent surface chemistry in twisted few-layer graphene. Using mid-infrared near-field optical microscopy and atomic force microscopy, we observe a selective adhesion of metallic nanoparticles and liquid water at the domains with rhombohedral stacking configurations of minimally twisted double bi- and trilayer graphene. Furthermore, we demonstrate that the manipulation of nanoparticles located at certain stacking domains can locally reconfigure the moiré superlattice in their vicinity at the micrometer scale. Our findings establish a new approach to controlling moiré-assisted chemistry and nanoengineering.