An etching system based on the interaction of electrons extracted from a direct current hollow cathode (HC) Ar plasma and injected toward an Si3N4 covered silicon substrate located in the downstream reactive environment created by an additional remote CF4/O2 plasma source was developed and evaluated. By controlling the properties of the injected beam electrons, this approach allows to deliver energy to a surface functionalized by exposure to reactive species and initiate surface etching. The energy of the primary beam electrons is controlled by the acceleration voltage relative to the HC discharge. Ar atoms flow from the high-pressure HC discharge into the low pressure downstream reactive environment in the process chamber. For an acceleration voltage greater than the ionization potential of Ar and/or process gas species, the energetic primary beam electrons produce a secondary plasma in the process chamber and can also cause additional dissociation. The authors have characterized the properties of the secondary plasma and also surface etching of Si3N4 as a function of process parameters, including acceleration voltage (0–80 V), discharge current of the HC discharge (1–2 A), pressure (3.5–20 mTorr), source to substrate distance (1.5–5 cm), and feed gas composition (20% and 80% O2 in CF4/O2). The electron energy probability function measured with a Langmuir probe about 2.5 cm below the extraction ring suggests several major groups of electrons for this situation, including high energy primary beam electrons with an energy that varies as the acceleration voltage is changed and low-energy electrons produced by beam electron-induced ionization of the Ar gas in the process chamber. When a remote CF4/O2 plasma is additionally coupled to the process chamber, Si3N4 surfaces can be functionalized, and by varying the energy of the beam electrons, Si3N4 etching can be induced by electron-neutral synergy effect with plasma-surface interaction. For conditions without beam electron injection, the remote plasma etching rate of Si3N4 depends strongly on the O2 concentration in the CF4/O2 processing gas mixture and can be suppressed for O2-rich process conditions by the formation of an SiONF passivation layer on the Si3N4 surface. The combination of the HC electron beam (HCEB) source with the remote plasma source makes it possible to induce Si3N4 etching for O2-rich remote plasma conditions where remote plasma by itself produces negligible Si3N4 etching. The electron enhanced etching of Si3N4 depends strongly on the O2/CF4 mixing ratio reflecting changing arrival rates of O and F species at the surface. Optical emission spectroscopy was used to estimate the ratio of gas phase F and O densities and found to be controlled by the gas mixing ratio and independent of HCEB operating conditions. At this time, the detailed sequence of events operative in the etching mechanism is unclear. While the increase of the electron energy is ultimately responsible for initiating surface etching, presently, the authors cannot rule out a role of ions from the simultaneously produced secondary plasma in plasma-surface interaction mechanisms.