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Tsedenia A. Zewdie

Publications and source records attributed to Tsedenia A. Zewdie.

2 recordsLinked to original sources

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 multifold 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↗

Ultrafast light-induced formation of a metastable hidden state in bismuth vanadate

Bismuth vanadate (BiVO$_4$) is a key photocatalyst for solar fuel applications, yet fundamental questions remain regarding the nature of photogenerated polaronic states and the lattice dynamics that govern its light-to-chemical pathways. Here, we use femtosecond optical pump-X-ray probe measurements to track the photoinduced electronic and structural dynamics in BiVO$_4$ across multiple length and time scales. Transient X-ray absorption spectroscopy captures sub-picosecond electron localization within VO$_4$ tetrahedra, consistent with small polaron formation, whereas time-resolved X-ray diffraction reveals a slower, multi-picosecond lattice reorganization into a hidden photoexcited state that is structurally distinct from both the monoclinic ground state and the high-temperature tetragonal phase. Supported by density functional theory, we show that hole-lattice interactions dynamically reduce the ground state monoclinic distortion, stabilizing the hidden state. Our results demonstrate that electron- and hole-lattice coupling jointly shape the excited state landscape, with implications for carrier transport, interfacial energetics, and light-to-chemical energy conversion pathways.

cond-mat.mtrl-sci↗