Issue 12, 2020

Plasma CVD of B–C–N thin films using triethylboron in argon–nitrogen plasma

Abstract

Amorphous boron–carbon–nitrogen (B–C–N) films with low density are potentially interesting as alternative low-dielectric-constant (low-κ) materials for future electronic devices. Such applications require deposition at temperatures below 300 °C, making plasma chemical vapor deposition (plasma CVD) a preferred deposition method. Plasma CVD of B–C–N films is today typically done with separate precursors for B, C and N or with precursors containing B–N bonds and an additional carbon precursor. We present an approach to plasma CVD of B–C–N films based on triethylboron (B(C2H5)3), a precursor with B–C bonds, in an argon–nitrogen plasma. From quantitative analysis with time-of-flight elastic recoil detection analysis (ToF-ERDA), we find that the deposition process can afford B–C–N films with a B/N ratio between 0.9–1.3 and B/C ratios between 3.4–8.6 and where the films contain from 3.6 to 7.8 at% H and from 6.6 to 20 at% O. The films have low density, from 0.32 to 1.6 g cm−3 as determined from cross-section scanning electron micrographs and ToF-ERDA with morphologies ranging from smooth films to separated nanowalls. Scanning transmission electron microscopy shows that C and BN do not phase-separate in the film. The static dielectric constant κ, measured by capacitance–voltage measurements, varies with the Ar concentration in the range from 3.3 to 35 for low and high Ar concentrations, respectively. We suggest that this dependence is caused by the energetic bombardment of plasma species during film deposition.

Graphical abstract: Plasma CVD of B–C–N thin films using triethylboron in argon–nitrogen plasma

Article information

Article type
Paper
Submitted
05 Feb 2020
Accepted
18 Feb 2020
First published
18 Feb 2020
This article is Open Access
Creative Commons BY license

J. Mater. Chem. C, 2020,8, 4112-4123

Plasma CVD of B–C–N thin films using triethylboron in argon–nitrogen plasma

L. Souqui, J. Palisaitis, H. Högberg and H. Pedersen, J. Mater. Chem. C, 2020, 8, 4112 DOI: 10.1039/D0TC00616E

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