Observation of Termination-Dependent Topological Connectivity in a Magnetic Weyl Kagome Lattice.

Engineering surfaces and interfaces of materials promises great potential in the field of heterostructures and quantum matter designers, with the opportunity to drive new many-body phases that are absent in the bulk compounds. Here, we focus on the magnetic Weyl kagome system Co3Sn2S2 and show how for the terminations of different samples the Weyl points connect differently, still preserving the bulk-boundary correspondence. Scanning tunneling microscopy has suggested such a scenario indirectly, and here, we probe the Fermiology of Co3Sn2S2 directly, by linking it to its real space surface distribution. By combining micro-ARPES and first-principles calculations, we measure the energy-momentum spectra and the Fermi surfaces of Co3Sn2S2 for different surface terminations and show the existence of topological features depending on the top-layer electronic environment. Our work helps to define a route for controlling bulk-derived topological properties by means of surface electrostatic potentials, offering a methodology for using Weyl kagome metals in responsive magnetic spintronics.

Synthesis, chiral crystal structure, and magnetic properties of Ba3Ga2O5Cl2.

A new compound, Ba3Ga2O5Cl2, isostructural with Ba3Fe2O5Cl2, was synthesized by solid-state reaction in air. Through single-crystal and powder X-ray diffraction analysis, the crystal structure was determined to be cubic with chiral space group I213 and unit-cell parameter a = 9.928 (1) Å. The Ga3+ ions in Ba3Ga2O5Cl2 are coordinated by O atoms and form GaO4 tetrahedra. Ten neighboring GaO4 tetrahedra are further bridged through corner sharing and rotation along the body diagonal, producing the chiral structure. Magnetization measurements indicate temperature-independent diamagnetic behavior, which is qualitatively consistent with core diamagnetism from all the constituent elements.

Spin Reorientation in Antiferromagnetic MnPd5Se with an Anti-CeCoIn5 Structure Type.

MnPd5Se, a derivative of the anti-CeCoIn5-type phase, was synthesized from a high-temperature solid-state reaction, structurally determined by X-ray diffraction, and magnetically characterized with a combined magnetic measurement and neutron powder diffraction (NPD). According to the X-ray diffraction results, MnPd5Se crystallizes in a layered tetragonal structure with the same space group as CeCoIn5, P4/mmm (No. 123). MnPd5Se shows antiferromagnetic ordering around 80 K on the basis of the magnetic property measurements. An A-type antiferromagnetic structure was revealed from the analysis of neutron powder diffraction results at 300, 50, and 6 K. Moreover, a spin orientation rotation was observed as the temperature decreased. Pd L3 X-ray absorption near edge spectroscopy results for MnPd5Se semiqualitatively correlate with the calculated density of states supporting a nominal 0.2 electron transfer into the Pd d orbital from either Se or Mn in the compound. The discovery of MnPd5Se, along with our previously reported MnT5Pn (T = Pd or Pt; Pn = P or As), provides a tunable system for studying the magnetic ordering from ferromagnetism to antiferromagnetism with the strong spin-orbit coupling effect.

Spin stiffness of chromium-based van der Waals ferromagnets.

Low temperature magnetization of CrI3, CrSiTe3and CrGeTe3single crystals were systematically studied. Based on the temperature dependence of extrapolated spontaneous magnetization from magnetic isotherms measured at different temperatures, the spin stiffness constant (D) and spin excitation gap (Δ) were extracted according to Bloch's law. For spin stiffness,Dis estimated to be 27 ± 6 meV Å2, 20 ± 3 meV Å2and 38 ± 7 meV Å2for CrI3, CrSiTe3and CrGeTe3respectively. Spin excitation gaps determined via Bloch's formulation have larger error bars yielding 0.59 ± 0.34 meV (CrI3), 0.37 ± 0.22 meV (CrSiTe3) and 0.28 ± 0.19 meV (CrGeTe3). Among all three studied compounds, larger spin stiffness value leads to higher ferromagnetic transition temperature.

Low-Temperature Fusible Silver Micro/Nanodendrites-Based Electrically Conductive Composites for Next-Generation Printed Fuse-Links.

We systematically investigate the long-neglected low-temperature fusing behavior of silver micro/nanodendrites and demonstrate the feasibility of employing this intriguing property for the printed electronics application, i.e., printed fuse-links. Fuse-links have experienced insignificant changes since they were invented in the 1890s. By introducing silver micro/nanodendrites-based electrically conductive composites (ECCs) as a printed fusible element, coupled with the state-of-the-art printed electronics technology, key performance characteristics of a fuse-link are dramatically improved as compared with the commercially available counterparts, including an expedient fabrication process, lower available rated current (40% of the minimum value of Littelfuse 467 series fuses), shorter response time (only 3.35% of the Littelfuse 2920L030 at 1.5 times of the rated current), milder surface temperature rise (16.89 °C lower than FGMB) and voltage drop (only 24.26% of FGMB) in normal operations, easier to mass produce, and more flexible in product design. This technology may inspire the development of future printed electronic components.