Spatially-resolved methane decomposition in a short glow discharge: insights into suprathermal hydrogen and radical chemistry
Abstract
This work presents the spatially resolved mapping of methane decomposition chemistry in a short direct-current glow discharge, revealing segregated zones for dissociation and polymerization in an Ar-CH4 mixture at 400 mTorr. Laser-induced fluorescence (LIF), two-photon absorption LIF (TALIF), and optical emission spectroscopy (OES), are used to map the absolute number densities of atomic hydrogen (H), methylidyne (CH), and dicarbon (C2) radicals. The results reveal a segregated chemical environment driven by the non-local electron kinetics. The primary dissociation of methane is confined to the cathode sheath (< 4 mm), where the H atom density peaks at a value (). Analysis of the Halpha} line profile identifies two distinct suprathermal H atom populations with peak kinetic energies of ~110 eV and ~17.5 eV, attributed to ion-surface reflection and electron-impact dissociation, respectively. The densities of secondary radicals CH and C2 peak further from the cathode at the sheath-negative glow boundary (y=4-6 mm), identifying this region as the primary zone for polymerization, with the peak C2 density higher than that of CH by a factor of ~370. The discharge operates under strong non-equilibrium conditions, confirmed by the disparity between the low bulk gas temperature (~570 K) and the high vibrational temperature (3300-4700 K) of the emitting CH(A) radicals, the latter serving as a signature of a specific high-energy dissociative excitation pathway. This work demonstrates how the structured energy landscape of a short glow discharge spatially separates methane dissociation from subsequent polymerization. Kinetic estimates suggest that suprathermal H atoms may play a role in bulk plasma chemistry via abstraction reactions, with predicted CH4 activation rates exceeding those of the thermal H population.
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BibTeX
@misc{yatom2026spatiallyresolved,
title = {{Spatially-resolved methane decomposition in a short glow discharge: insights into suprathermal hydrogen and radical chemistry}},
author = {Shurik Yatom},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2609.17345},
eprint = {2609.17345},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2609.17345},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - Spatially-resolved methane decomposition in a short glow discharge: insights into suprathermal hydrogen and radical chemistry
AU - Shurik Yatom
PY - 2026
DA - 2026/09/15
PB - arXiv
DO - 10.48550/arxiv.2609.17345
UR - https://arxiv.org/abs/2609.17345
AB - This work presents the spatially resolved mapping of methane decomposition chemistry in a short direct-current glow discharge, revealing segregated zones for dissociation and polymerization in an Ar-CH4 mixture at 400 mTorr. Laser-induced fluorescence (LIF), two-photon absorption LIF (TALIF), and optical emission spectroscopy (OES), are used to map the absolute number densities of atomic hydrogen (H), methylidyne (CH), and dicarbon (C2) radicals. The results reveal a segregated chemical environment driven by the non-local electron kinetics. The primary dissociation of methane is confined to the cathode sheath (< 4 mm), where the H atom density peaks at a value (). Analysis of the Halpha} line profile identifies two distinct suprathermal H atom populations with peak kinetic energies of ~110 eV and ~17.5 eV, attributed to ion-surface reflection and electron-impact dissociation, respectively. The densities of secondary radicals CH and C2 peak further from the cathode at the sheath-negative glow boundary (y=4-6 mm), identifying this region as the primary zone for polymerization, with the peak C2 density higher than that of CH by a factor of ~370. The discharge operates under strong non-equilibrium conditions, confirmed by the disparity between the low bulk gas temperature (~570 K) and the high vibrational temperature (3300-4700 K) of the emitting CH(A) radicals, the latter serving as a signature of a specific high-energy dissociative excitation pathway. This work demonstrates how the structured energy landscape of a short glow discharge spatially separates methane dissociation from subsequent polymerization. Kinetic estimates suggest that suprathermal H atoms may play a role in bulk plasma chemistry via abstraction reactions, with predicted CH4 activation rates exceeding those of the thermal H population.
ER -