Thermal Stability and Rehybridization of Carbon Bonding in Tetrahedral Amorphous Carbon

نویسندگان

  • David S. Grierson
  • Andrew Konicek
  • J P. Sullivan
  • Robert W. Carpick
  • D. S. Grierson
  • A. V. Sumant
  • A. R. Konicek
  • T. A. Friedmann
  • J. P. Sullivan
چکیده

We preform a quantitative investigation of the energetics of thermally induced sp3 → sp2 conversion of carboncarbon bonds in tetrahedral amorphous carbon (ta-C) films by using near edge x-ray absorption fine structure (NEXAFS) and Raman spectroscopy. We investigate the evolution of the bonding configuration in ta-C thin films subjected to high temperature annealing in flowing Argon gas using a rapid thermal annealing furnace over the range of 200-1000 oC. We observe no substantial change in bonding structure below 600 oC, and by 1000 oC a significant increase in the sp2 bonding in the film is observed. No oxygen bonding is detected in the NEXAFS spectra, but we do observe an isosbestic point, demonstrating that the thermally driven sp3 → sp2 conversion reaction occurs without passing through an intermediate transition state. This allows us to use NEAFS spectra of thermally annealed ta-C films to quantitatively determine that the activation energy for directly converting the sp3-bonded carbon to the sp

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

MAGNETISATION AND ELECTRON SPIN RESONANCE STUDIES OF TETRAHEDRAL AMORPHOUS CARBON

The magnetisation and electron spin resonance (ESR) spectrum of two specimens of tetrahedral amorphous carbon (ta-C), deposited from a filtered cathodic arc, were measured over a wide temperature range. The magnetisation was found to consist of superparamagnetic, paramagnetic and diamagnetic contributions. The superparamagnetic contribution resembled that recently found in carbon prepared from ...

متن کامل

Wear, Plasticity, and Rehybridization in Tetrahedral Amorphous Carbon

Wear in self-mated tetrahedral amorphous carbon (ta-C) films is studied by molecular dynamics and nearedge X-ray absorption fine structure spectroscopy. Both theory and experiment demonstrate the formation of a soft amorphous carbon (a-C) layer with increased sp content, which grows faster than an a-C tribolayer found on selfmated diamond sliding under similar conditions. The faster sp ! sp tra...

متن کامل

Photoconductivity in highly tetrahedral diamondlike amorphous carbon

A photoconductive effect is observed in tetrahedral amorphous carbon (ta-C) or amorphous diamond films with a high proportion of sp3 bonding and a structure analogous to amorphous silicon. The spectral response is shown to peak at around 750400 nm and extend into the near UV region. The maximum photoresponse coincides wit.h the optical absorption edge. The quantum efficiency of 300 nm thick fil...

متن کامل

Stress reduction and bond stability during thermal annealing of tetrahedral amorphous carbon

A comprehensive study of the stress release and structural changes caused by postdeposition thermal annealing of tetrahedral amorphous carbon ~ta-C! on Si has been carried out. Complete stress relief occurs at 600–700 °C and is accompanied by minimal structural modifications, as indicated by electron energy loss spectroscopy, Raman spectroscopy, and optical gap measurements. Further annealing i...

متن کامل

uv Studies of Tetrahedral Bonding in Diamondlike Amorphous Carbon

We report ultraviolet (uv) Raman scattering studies of hydrogen-free, diamondlike amorphous carbon thin films with a wide range of tetrahedral bonding. The uv Raman spectra are shown to provide direct evidence for the presence of sp-bonded C atoms in these materials. The experimental results are found to be in excellent agreement with theoretical predictions and contribute to an improved unders...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013