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Laura I. Wagner

Publications and source records attributed to Laura I. Wagner.

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Al$_{1-x}$Hf$_{x}$N Thin Films with Enhanced Piezoelectric Responses for GHz Surface Acoustic Wave Devices

Ternary compounds obtained by alloying wurtzite AlN with transition metals have emerged as promising materials with significantly enhanced piezoelectric characteristics relative to binary AlN. The increased electromechanical coupling in these compounds boosts the performance of high-frequency acoustic devices. So far, progress has largely focused on Al$_{1-x}$Sc$_x$N, which is costly and poorly compatible with complementary metal-oxide-semiconductor (CMOS) technologies. Here, we investigate aluminum hafnium nitride (Al$_{1-x}$Hf$_{x}$N) as a scalable and potentially CMOS-compatible alternative to Al$_{1-x}$Sc$_x$N. Using reactive co-sputtering on both Si and sapphire substrates, we demonstrate wurtzite Al$_{1-x}$Hf$_{x}$N thin films ($x \leq 0.17$) with strong $c$-axis texture and nearly isotropic lattice expansion upon Hf incorporation. X-ray absorption spectroscopy indicates cross-gap hybridization between N 2$p$ and Hf 5$d$ states, which can enhance the Born effective charge and, thereby, the piezoelectric response. Correspondingly, we observe a nearly two-fold enhancement in the piezoelectric coefficient, $d_{33}$, relative to AlN, despite increasing structural disorder in Al$_{1-x}$Hf$_{x}$N. Building on this finding, we demonstrate Al$_{1-x}$Hf$_{x}$N GHz surface acoustic wave (SAW) resonators that exhibit enhanced performance, as well as efficient excitation of bulk acoustic waves with low propagation losses. These results establish Al$_{1-x}$Hf$_{x}$N as a promising platform for next-generation high-frequency electromechanical devices, with prospects for further piezoelectric enhancements through improved epitaxy.

cond-mat.mtrl-sci

Quantifying Thermal, Photovoltage, and Defect Contributions to Transient Absorption of Ta$_{3}$N$_{5}$ Photoanodes

Ta$_{3}$N$_{5}$ is among the most intensively studied photoanode materials for solar-driven water oxidation, yet its performance often remains limited by short carrier lifetimes and defect mediated recombination. Although transient absorption spectroscopy is widely used to probe carrier dynamics in photoelectrodes, spectral assignments are frequently ambiguous due to overlapping contributions. Here, microsecond-to-second transient absorption of Ta$_{3}$N$_{5}$ thin films is combined with complementary optical spectroscopies to disentangle contributions from lattice heating, electrostatics, and defect states. Photoreflectance reveals three critical points in the Ta$_{3}$N$_{5}$ band structure, including two anisotropic near-edge transitions at 2.14 eV and 2.27 eV and a higher-lying transition near 2.80 eV, all closely aligned with dominant transient absorption features. A previously unreported photo-induced absorption at 2.80 eV is attributed to pump-induced lattice heating, while potential-dependent measurements reveal that near-edge bleach features arise from pump-induced band flattening and subsequent surface photovoltage relaxation. Fitting transient absorption spectra with independently measured thermal and electrostatic components enables quantification of both thermal and photovoltage dynamics, while the sub-bandgap response provides insight into the redistribution of defect charge states. Thus, this approach to quantifying thermal, electrostatic, and defect-mediated contributions to microsecond-to-second transient absorption provides broadly applicable insights into photoexcitation and relaxation mechanisms in functional semiconductor photoelectrodes.

cond-mat.mtrl-sci