Abstract

Various mechanisms have been proposed to explain photo-assisted etching (PAE) of Si, including photogenerated carrier-mediated etching, photon-stimulated desorption, and photon-induced damage (breaking of Si–Si bonds) caused mainly by vacuum ultraviolet photons irradiating the substrate. In this study, the authors use optical emission spectroscopy to gain an insight into possible in-plasma PAE mechanisms. Emissions from Cl, Si, SiCl, and Ar were recorded as a function of power while etching p-Si in Cl2/Ar Faraday-shielded inductively coupled plasmas at a pressure of 60 mTorr with no substrate bias. Under these conditions, ion-assisted etching was negligible and PAE was dominant. The Si:Ar optical emission intensity ratio, ISi/IAr (proportional to the etching rate of Si), increased substantially with power. Accounting for the contribution to this signal from the dissociation of SiClx (x = 1–4) etch products, the residual increase in the emission indicated that the PAE rate also increased with power. Time resolved emissions were also recorded in a pulsed plasma where power was modulated between 500 and 300 W. ISi/IAr was found to modulate with the instantaneous power. This rules out the photon-induced damage mechanism since, if this mechanism was dominant, the ISi/IAr signal would not be modulated.

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