Developing catalysts with high activity, durability, and water resistance for ozone decomposition is crucial to regulate the pollution of ozone in the troposphere, especially in indoor air. To overcome the shortcomings of metal oxide catalysts with respect to their durability and water resistance, Fe-Co double-atom catalyst (DAC) is proposed as a novel catalyst for ozone decomposition. Here, through a systematic study using density functional theory (DFT) calculations and microkinetic modeling, the adsorption and catalytic decomposition of O3 on Fe-Co DAC have been examined based on adsorption configuration, orbital hybridization, and electron transfer. Based on Eley-Rideal (E-R) and Langmuir-Hinshelwood (L-H) reaction mechanisms, the mechanisms of ozone decomposition on Fe-Co DAC were explored by analyzing reaction paths and energy variations. To confirm the water-resistant of Fe-Co DAC, competitive adsorption behavior between O3 and dominant environmental gases was discussed through ab initio molecular dynamic (AIMD) simulation. The dominant reaction mechanism of ozone decomposition is L-H and the rate-determining step is the desorption of the first oxygen molecule from the surface of Fe-Co DAC which has an energy barrier of 0.78 eV. Due to this relatively low energy barrier and high turnover frequency (TOF), the optimal operation window of catalytic O3 decomposition on Fe-Co DAC is <500 K suggesting that catalytic decomposition of O3 on Fe-Co DAC can occur at room temperature. This theoretical study provides new insights for designing novel catalysts for ozone decomposition and fundamental guidance for subsequent experimental research.
Keywords: Catalytic decomposition; Competitive adsorption; Double-atom catalyst; Microkinetic modeling; Ozone; Water resistance.
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