Regulation Lattice Oxygen Mobility via Dual Single Atoms for Simultaneously Enhancing VOC Oxidation and NO<sub><i>x</i></sub> Reduction

Synergistic catalytic removal of multipollutants (e.g., volatile organic compound (VOC) oxidation and nitrogen oxide (NO<sub><i>x</i></sub>) reduction) is highly demanded due to the increasingly strict emission standards. The prevention of the key reactive intermediate species nitrite excessive oxidation over the supported noble-metal catalysts, rather than the traditional low-efficiency transition metal oxide catalysts, remains a great challenge. Herein, a sound strategy of Pd single atoms saturated with acidic transition element ligands is proposed. The coexistence of Pd and V dual single atoms strengthens the adsorption of reactants, while synergistic interaction between dual atoms and surface oxygen weakens activation of lattice oxygen, thus significantly reducing the overoxidation of nitrite. Meanwhile, the neutralization of the active Pd and inert V sites results in a rational decrease in the redox property of Pd and an obvious increase in that of V. The Pd<sub>1</sub>V<sub>1</sub>/CeO<sub>2</sub> dual single-atom catalyst achieves 90% conversion of NO<sub><i>x</i></sub> and toluene at 238 and 230 °C and has a large temperature window (>150 °C) for NO<sub><i>x</i></sub> reduction. This research makes a breakthrough in the development of efficient supported noble-/transition-metal dual single-atom catalysts for VOC and NO<sub><i>x</i></sub> simultaneous purification.

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Publication Details

Journal
Environmental Science & Technology
Published
2024-09-16
DOI
https://doi.org/10.1021/acs.est.4c03049
Citations
36
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
4.22

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article

Regulation Lattice Oxygen Mobility via Dual Single Atoms for Simultaneously Enhancing VOC Oxidation and NOx Reduction

Zhiwei Wang, Peiqi Chu, Zhenxia Zhao, Yuxi Liu et al.
36 citations
Environmental Science & Technology
Catalytic Processes in Materials Science
4.22
article

Regulation Lattice Oxygen Mobility via Dual Single Atoms for Simultaneously Enhancing VOC Oxidation and NOx Reduction

Zhiwei Wang, Peiqi Chu, Zhenxia Zhao, Yuxi Liu, Jiguang Deng, Long Zhang, Wei Lü, Guangsheng Guo, Hongxing Dai, Erhong Duan
article en
36 citations

Abstract

Synergistic catalytic removal of multipollutants (e.g., volatile organic compound (VOC) oxidation and nitrogen oxide (NO<sub><i>x</i></sub>) reduction) is highly demanded due to the increasingly strict emission standards. The prevention of the key reactive intermediate species nitrite excessive oxidation over the supported noble-metal catalysts, rather than the traditional low-efficiency transition metal oxide catalysts, remains a great challenge. Herein, a sound strategy of Pd single atoms saturated with acidic transition element ligands is proposed. The coexistence of Pd and V dual single atoms strengthens the adsorption of reactants, while synergistic interaction between dual atoms and surface oxygen weakens activation of lattice oxygen, thus significantly reducing the overoxidation of nitrite. Meanwhile, the neutralization of the active Pd and inert V sites results in a rational decrease in the redox property of Pd and an obvious increase in that of V. The Pd<sub>1</sub>V<sub>1</sub>/CeO<sub>2</sub> dual single-atom catalyst achieves 90% conversion of NO<sub><i>x</i></sub> and toluene at 238 and 230 °C and has a large temperature window (>150 °C) for NO<sub><i>x</i></sub> reduction. This research makes a breakthrough in the development of efficient supported noble-/transition-metal dual single-atom catalysts for VOC and NO<sub><i>x</i></sub> simultaneous purification.

Environmental Science & TechnologyVol. 58(39)
Guangxi University (CN), Hebei University of Science and Technology (CN), Beijing University of Technology (CN)
National Natural Science Foundation of China, Beijing Municipal Education Commission, Natural Science Foundation of Hebei Province
Clean water and sanitation
Openalex Percentile: Top 3%
Catalytic Processes in Materials Science
4.22
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