AVS 64th International Symposium & Exhibition | |
Plasma Science and Technology Division | Monday Sessions |
Session PS+AS+SS-MoA |
Session: | Plasma Surface Interactions |
Presenter: | Chen Li, University of Maryland, College Park |
Authors: | C. Li, University of Maryland, College Park T. Hofmann, Carl Zeiss SMT GmbH K. Edinger, Carl Zeiss SMT GmbH G.S. Oehrlein, University of Maryland, College Park |
Correspondent: | Click to Email |
Plasma etching processes capable of highly selective Si3N4 to SiO2 removal are increasingly required in fabrication of current integrated circuit devices. We report fluorocarbon (FC) based remote plasma etching processes for Si3N4 and SiO2 substrates using inductively coupled plasma (ICP) and electron cyclotron wave resonance (ECWR) plasma reactors. For the remote plasma operating conditions direct ion bombardment of the sample surface is prevented and etching is primarily due to chemical reactions by neutral radicals. Such conditions can be realized by either high processing pressure for a remote ICP source or a neutralization plate for an ECWR source. Combinations of fluorocarbon gases, e.g. CF4, with O2 and N2 additives have been evaluated. Etching behavior and surface properties are monitored using in situ ellipsometry. Optical emission spectroscopy (OES) has been used to evaluate the plasma gas phase chemistry. We show that ultra-high Si3N4 to SiO2 etching selectivity can be achieved under remote plasma conditions in both reactors, and that control of the feed gas chemistry plays a key role. As is well-known, low levels of O2 increase oxidation of FC gases and atomic F generation, which leads to increasing Si3N4 etch rate, whereas for high O2 levels the F concentration is reduced and surface oxidation takes place. For these F-rich remote plasma conditions, SiO2 is hardly etched and Si3N4 to SiO2 etching selectivity of 7 and 87 were observed for the ICP and ECWR system, respectively. The observed etching behavior will be discussed using surface chemical studies of Si3N4 and SiO2 by vacuum transferred x-ray photoelectron spectroscopy (XPS).