Twisted charge-density-wave patterns in bilayer 2D crystals and modulated electronic states

The twistronics of the atomic-thick two-dimensional (2D) van der Waals materials has opened a new venue to investigate the interlayer coupling. Till now, most studies focus on the twist of atomic lattices and the resulted moiré superstructures, while the reports about the twist of charge density waves (CDW), the superstructures of which are from individual layers are limited. Here, using molecular beam epitaxy, we construct bilayer (BL) 1T-NbSe2 vertical structures. With high resolution scanning tunneling microscopy observations, we identify two cases of CDW twisted stacking with atomic precision. The typical twist angles are 0o and 60o between the 1st and the 2nd layer, although the top Se atomic lattices of these two layers are parallel. Compared to the single layer case, the dI/dV at BL shows an insulator-to-metal transition, with the Hubbard bands shrinking towards the Fermi level (EF ). More intriguingly, interlayer coupling states rise near EF , which are dependent on the CDW twist angles. These findings give fresh insight into the engineering of 2D materials by CDW twisting and are potentially applicable for future nanoelectronic devices.

Skyrmion lattice creep at ultra-low current densities

Magnetic skyrmions are well-suited for encoding information because they are nano-sized, topologically stable, and only require ultra-low critical current densities jc to depin from the underlying atomic lattice. Above jc skyrmions exhibit well-controlled motion, making them prime candidates for race-track memories. In thin films thermally-activated creep motion of isolated skyrmions was observed below jc as predicted by theory. Uncontrolled skyrmion motion is detrimental for race-track memories and is not fully understood. Notably, the creep of skyrmion lattices in bulk materials remains to be explored. Here we show using resonant ultrasound spectroscopy—a probe highly sensitive to the coupling between skyrmion and atomic lattices—that in the prototypical skyrmion lattice material MnSi depinning occurs at $${j}_{c}^{* }$$ j c * that is only 4 percent of jc. Our experiments are in excellent agreement with Anderson-Kim theory for creep and allow us to reveal a new dynamic regime at ultra-low current densities characterized by thermally-activated skyrmion-lattice-creep with important consequences for applications.

Recent advances in 2D, 3D and higher-order topological photonics

Over the past decade, topology has emerged as a major branch in broad areas of physics, from atomic lattices to condensed matter. In particular, topology has received significant attention in photonics because light waves can serve as a platform to investigate nontrivial bulk and edge physics with the aid of carefully engineered photonic crystals and metamaterials. Simultaneously, photonics provides enriched physics that arises from spin-1 vectorial electromagnetic fields. Here, we review recent progress in the growing field of topological photonics in three parts. The first part is dedicated to the basics of topological band theory and introduces various two-dimensional topological phases. The second part reviews three-dimensional topological phases and numerous approaches to achieve them in photonics. Last, we present recently emerging fields in topological photonics that have not yet been reviewed. This part includes topological degeneracies in nonzero dimensions, unidirectional Maxwellian spin waves, higher-order photonic topological phases, and stacking of photonic crystals to attain layer pseudospin. In addition to the various approaches for realizing photonic topological phases, we also discuss the interaction between light and topological matter and the efforts towards practical applications of topological photonics.

Three-dimensional superlattice engineering with block copolymer epitaxy

Three-dimensional (3D) structures at the nanometer length scale play a crucial role in modern devices, but their fabrication using traditional top-down approaches is complex and expensive. Analogous to atomic lattices, block copolymers (BCPs) spontaneously form a rich variety of 3D nanostructures and have the potential to substantially simplify 3D nanofabrication. Here, we show that the 3D superlattice formed by BCP micelles can be controlled by lithographically defined 2D templates matching a crystallographic plane in the 3D superlattice. Using scanning transmission electron microscopy tomography, we demonstrate precise control over the lattice symmetry and orientation. Excellent ordering and substrate registration can be achieved, propagating through 284-nanometer-thick films. BCP epitaxy also showed exceptional lattice tunability, with a continuous Bain transformation from a body-centered cubic to a face-centered cubic lattice. Lattice stability was mediated by molecular packing frustration, and surface-induced lattice reconstruction was observed, leading to the formation of a unique honeycomb lattice.