Gavin B. Osterhoudt

Local phonon mode in thermoelectric Bi2Te2Se from charge neutral antisites

Local modes caused by defects play a significant role in the thermal transport properties of thermoelectrics. Of particular interest are charge-neutral defects that suppress thermal conductivity, without significantly reducing electrical transport. Here, we report a temperature dependent Raman study that identifies such a mode in a standard thermoelectric material, Bi2Te2Se. One of the modes observed, whose origin has been debated for decades, was shown most likely to be an antisite defect induced local mode. The anomalous temperature independent broadening of the local mode is ascribed to the random arrangement of Se atoms. The temperature renormalization of all modes is well explained by an anharmonic model–Klemenss model.

Low vibration high numerical aperture automated variable temperature Raman microscope

Raman micro-spectroscopy is well suited for studying a variety of properties and has been applied to a wide range of areas. Combined with tuneable temperature, Raman spectra can offer even more insights into the properties of materials. However, previous designs of variable temperature Raman microscopes have made it extremely challenging to measure samples with low signal levels due to thermal and positional instabilities as well as low collection efficiencies. Thus contemporary Raman microscope has found limited applicability to probing the subtle physics involved in phase transitions and hysteresis. This paper describes a new design of a closed-cycle, Raman microscope with full polarization rotation. High collection efficiency, thermal stability, and mechanical stability are ensured by both deliberate optical, cryogenic, and mechanical design. Measurements on two samples, Bi2Se3 and V2O3, which are challenging due to low thermal conductivities, low signal levels, and/or hysteretic effects, are measured with previously undemonstrated temperature resolution.

Controlling Magnetic and Optical Properties of the van der Waals Crystal CrCl3−xBrx via Mixed Halide Chemistry

Magnetic van der Waals (vdW) materials are the centerpiece of atomically thin devices with spintronic and optoelectronic functions. Exploring new chemistry paths to tune their magnetic and optical properties enables significant progress in fabricating heterostructures and ultracompact devices by mechanical exfoliation. The key parameter to sustain ferromagnetism in 2D is magnetic anisotropy-a tendency of spins to align in a certain crystallographic direction known as easy-axis. In layered materials, two limits of easy-axis are in-plane (XY) and out-of-plane (Ising). Light polarization and the helicity of topological states can couple to magnetic anisotropy with promising photoluminescence or spin-orbitronic functions. Here, a unique experiment is designed to control the easy-axis, the magnetic transition temperature, and the optical gap simultaneously in a series of CrCl3-x Brx crystals between CrCl3 with XY and CrBr3 with Ising anisotropy. The easy-axis is controlled between the two limits by varying spin-orbit coupling with the Br content in CrCl3-x Brx . The optical gap, magnetic transition temperature, and interlayer spacing are all tuned linearly with x. This is the first report of controlling exchange anisotropy in a layered crystal and the first unveiling of mixed halide chemistry as a powerful technique to produce functional materials for spintronic devices.

Possible structural transformation and enhanced magnetic fluctuations in exfoliated α-RuCl3

Abstract We present Raman spectroscopy experiments on exfoliated α -RuCl 3 , from tens of nm thick down to single layers. Besides unexpectedly finding this material to be air stable, in the thinnest layers we observe the appearance with decreasing temperature of a symmetry-forbidden mode in crossed polarization, along with an anomalous broadening of a mode at 164 cm −1 that is known to couple to a continuum of magnetic excitations. This may be due to an enhancement of magnetic fluctuations and evidence for a distorted honeycomb lattice in single- and bilayer samples.