arXiv subjects

Antonius Armanious

Publications and source records attributed to Antonius Armanious.

4 recordsLinked to original sources

arXiv2026

Reduction of intrinsic losses in nanomechanical silicon nitride resonators through thermal treatment in ultrahigh vacuum

Since the discovery of dissipation dilution, silicon nitride (SiN) nanomechanical resonators have set the benchmark for ultracoherent mechanical systems, with geometry and strain engineering driving remarkable gains in the $f \cdot Q$ product. Surface loss, however, has remained the dominant and largely unaddressed dissipation channel. Here, we demonstrate a geometry-independent approach that directly targets surface loss: thermal treatment in ultrahigh vacuum. Treatment at 1000$^{\circ}$C enhances the intrinsic quality factor of dissipation-diluted SiN membrane resonators by up to a factor of 20, reduces the surface loss eightfold, and simultaneously increases the tensile stress. Photothermal infrared spectroscopy and $\textit{in situ}$ X-ray photoelectron spectroscopy trace the enhancement to thermally activated silanol condensation - the conversion of surface hydroxyl terminations into siloxane bridges - and the reversibility of both quality factor and stress under controlled humidity confirms the surface-chemical origin. These results establish surface chemistry as a tunable parameter for next-generation ultracoherent nanomechanical resonators.

physics.app-ph↗

arXiv2026

HF Etching and Silanization: Evidence for the Role of Surface Hydroxyl Groups in Silicon Nitride Resonator Loss

Silicon nitride $SiN_x$ nanomechanical resonators are central to sensing, quantum technologies, and fundamental physics experiments due to their exceptional mechanical quality factors (Q). However, as resonator thickness approaches the nano-scale, surface-related dissipation limits performance. Here, we investigate the role of surface chemistry in low-stress Si-rich SiNx membranes through a combination of hydrofluoric acid (HF) etching and trimethylchlorosilane (TMCS) silanization, correlated with surface characterization and mechanical measurements. Preliminary analysis by TEM-EELS, XPS, RBS/ERDA, and XRR reveals a native oxide surface layer (1-2 nm). Surface modification by HF and TMCS was subsequently evaluated using XPS, photothermal FTIR, contact-angle measurements, and intrinsic quality factor ($Q_{int}$) characterization. While HF etching effectively removes the native oxide and TMCS introduces hydrophobic $Si-(CH_3)_3$ termination, neither oxide thickness nor surface energy correlates with mechanical dissipation. TMCS treatments produce the largest enhancements, increasing $Q_{int}$ by up to 50%, whereas HF etching alone yields lower gains of 20-25%. These findings suggest surface hydroxyl groups as a key contributor to energy loss in $SiN_x$ resonators and demonstrate that chemical functionalization can substantially suppress surface dissipation.

cond-mat.mtrl-sci↗

arXiv2026

Determination of the intrinsic mechanical quality factor in high-stress silicon nitride resonators

Recent advances in silicon nitride nanomechanical resonators have pushed mechanical quality factors to ultra-high values by combining stress-induced dissipation dilution with mode-shape engineering. Neither mechanism alters the intrinsic quality factor $Q_{\mathrm{intr}}$. Targeting the intrinsic loss itself therefore remains an untapped route to even higher $Q$. Doing so first requires reliable quantification of $Q_{\mathrm{intr}}$, which has proven challenging. Here we present a robust methodology that quantifies $Q_{\mathrm{intr}}$ by combining automated mode identification with systematic ringdown measurements over a large number of mechanical modes. Applied to high-stress silicon nitride membranes, it reveals a systematic dependence of $Q_{\mathrm{intr}}$ on thickness that cannot be described using established models, particularly in the ultra-thin limit. We account for this trend with a phenomenological model that incorporates a thickness-dependent loss channel. Together, our method and model open a route toward a microscopic understanding of intrinsic dissipation and toward directly mitigating its loss channels.

physics.app-ph↗

arXiv2021

Determination of Nano-sized Adsorbate Mass in Solution using Mechanical Resonators: Elimination of the so far Inseparable Liquid Contribution

Assumption-free mass quantification of nanofilms, nanoparticles, and (supra)molecular adsorbates in liquid environment remains a key challenge in many branches of science. Mechanical resonators can uniquely determine the mass of essentially any adsorbate; yet, when operating in liquid environment, the liquid dynamically coupled to the adsorbate contributes significantly to the measured response, which complicates data interpretation and impairs quantitative adsorbate mass determination. Employing the Navier-Stokes equation for liquid velocity in contact with an oscillating surface, we show that the liquid contribution can be eliminated by measuring the response in solutions with identical kinematic viscosity but different densities. Guided by this insight, we used quartz crystal microbalance (QCM), one of the most widely-employed mechanical resonator, to demonstrate that kinematic-viscosity matching can be utilized to accurately quantify the dry mass of systems such as adsorbed rigid nanoparticles, tethered biological nanoparticles (lipid vesicles), as well as highly hydrated polymeric films. The same approach applied to the simultaneously measured energy dissipation made it possible to quantify the mechanical properties of the adsorbate and its attachment to the surface, as demonstrated by, for example, probing the hydrodynamic stablization induced by nanoparticles crowding. Finally, we envision that the possibility to simultaneously determine the dry mass and mechanical properties of adsorbates as well as the liquid contributions will provide the experimental tools to use mechanical resonators for applications beyond mass determination, as for example to directly interrogate the orientation, spatial distribution, and binding strength of adsorbates without the need for complementary techniques.

physics.app-ph↗