Abstract

The synthesis of silicon carbonitride by low-temperature plasma-enhanced chemical vapor deposition and the machining of nanomechanical resonators in this material are reported. Films with thickness of 1μm, 200nm, and 50nm were deposited using ammonia, nitrogen, and diethylsilane as precursors. X-ray photoelectron spectroscopy indicated that usage of higher NH3:DES gas flow ratios results in higher nitrogen and low carbon contents in the deposited films. In addition, annealing of the material enabled the full tunability of its residual stress from the compressive to the tensile range. Infrared spectroscopy indicated that desorption of incorporated hydrogen was responsible for those changes. Assaying of resonant cantilevers fabricated from 200-nm-thick films yielded root-modulus-over-density values as high as √(E∕ρ)=8.35×103m∕s, comparable to those of silicon. Doubly clamped beams were also fabricated from 50-nm-thick films of low (σ=80MPa) and high (σ=220MPa) tensile stresses. Beam resonators fabricated in the lower stress material showed resonance qualities ranging between 3000 and 5000, and resonant frequencies between f=6.1MHz and f=16MHz. Beam resonators machined in the higher stress material experienced quality factors between 8000 and 23 000 and frequencies between f=7.6 and 24MHz. These values correspond to fQ products as high as of 1.5×1011s−1, exceeding the performance of previously reported silicon resonators.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.