Abstract
Power-to-chemical technologies with CO(2) as feedstock recycle CO(2) and store energy into value-added compounds. Plasma discharges fed by renewable electricity are a promising approach to CO(2) conversion. However, controlling the mechanisms of plasma dissociation is crucial to improving the efficiency of the technology. We have investigated pulsed nanosecond discharges, showing that while most of the energy is deposited in the breakdown phase, CO(2) dissociation only occurs after an order of microsecond delay, leaving the system in a quasi-metastable condition in the intervening time. These findings indicate the presence of delayed dissociation mechanisms mediated by CO(2) excited states rather than direct electron impact. This "metastable" condition, favorable for an efficient CO(2) dissociation, can be prolonged by depositing more energy in the form of additional pulses and critically depends on a sufficiently short interpulse time.