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Elizabeth Grace Houser

Publications and source records attributed to Elizabeth Grace Houser.

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Vanadium doping induced valley asymmetries in WS$_2$ monolayers

Transition metal dichalcogenide (TMD) monolayers offer an innovative platform for encoding and manipulating information through the valley degree of freedom. While unique valley-related physical phenomena have been reported so far, practical applications still require advanced control over the valley polarization efficiency and the valley Zeeman effect. Recently, the introduction of spin-polarized metal atoms as substitutional defects was reported to break the time-reversal symmetry in TMD monolayers, consequently inducing a room-temperature ferromagnetic ordering and enhancing the valley-dependent optical responses. Here, we report valley asymmetries for vanadium-doped WS$_2$ monolayers. With a given magnetic polarization, one valley exhibits larger Zeeman slope and degree of circular polarization than the other valley. Additionally, the overall degree of circular polarization in the doped samples is approximately twice that of the pristine WS$_2$ monolayer. Density functional theory calculations in the doped structure show that different energy shifts in conduction band edges due to spin-dependent hybridization lead to different exciton energies between valleys, which is consistent with the experimental observations. Our results pave the way for valleytronic technologies based on defect-engineered two-dimensional materials.

cond-mat.mes-hall

Anisotropic Dopant and Strain Architectures in WS$_2$ Nanocrystals Driven by Growth Kinetics

Dopant distribution in two-dimensional semiconductors is typically assumed to be stochastic, limiting deterministic defect engineering. Here, we show that non-equilibrium growth kinetics can be harnessed to define dopant-driven strain architectures in vanadium-doped WS$_2$ monolayers. Using synchrotron X-ray fluorescence, we identify preferential vanadium incorporation, anti-correlated with tungsten content, along crystallographic bisectors. An adsorption-growth-diffusion model with a single kinetic parameter quantitatively captures the dopant segregation arising from preferential corner adsorption and limited diffusion during chemical vapor deposition growth. Hyperspectral Raman imaging demonstrates mechanically induced vibrational responses, revealing localized tensile strain ($\varepsilon \approx0.70\%$) channels associated with the anisotropic dopant distribution. This regime is marked by the depletion of W-site-sensitive in-plane modes and the emergence of a localized $J2$ mode (210~cm$^{-1}$), which our ab-initio calculations attribute to antiphase V$-$V oscillations. These findings establish kinetic segregation as a route to deterministic chemical and strain architectures in 2D semiconductors, enabling programmable defect landscapes and strain engineering during synthesis.

cond-mat.mtrl-sci