Insights into the Synergistic Promotion Effect of Cu and W Modification on the Catalytic Performance of α-Fe<sub>2</sub>O<sub>3</sub> for NH<sub>3</sub>-SCR of NO<i><sub><i>x</i></sub></i>

A dual-element modification strategy was proposed to promote the catalytic performance of the α-Fe<sub>2</sub>O<sub>3</sub> catalyst for the selective catalytic reduction of NO<i><sub><i>x</i></sub></i> by NH<sub>3</sub> (NH<sub>3</sub>-SCR of NO<i><sub><i>x</i></sub></i>) at both low and high temperatures. By optimizing the loading amount of CuO (4 wt %) and WO<sub>3</sub> (5 wt %), a wide operating temperature window (150-350 °C) was achieved on the modified α-Fe<sub>2</sub>O<sub>3</sub> catalyst (W<sub>5</sub>/Cu<sub>4</sub>/Fe). Further characterizations revealed that the enhanced low-temperature activity could be attributed to the improved redox performance of α-Fe<sub>2</sub>O<sub>3</sub> through CuO modification, while the superior high-temperature activity was primarily ascribed to the enhanced surface acidity induced by WO<sub>3</sub> modification. The synergistic effect of CuO and WO<sub>3</sub> modifications facilitated the NH<sub>3</sub>-SCR reaction on the modified α-Fe<sub>2</sub>O<sub>3</sub> catalysts to efficiently proceed through the Eley-Rideal (E-R) mechanism pathway. This provided compelling evidence that the catalytic performance of NH<sub>3</sub>-SCR catalysts at different temperatures was dominantly governed by distinct factors (e.g., redox property and surface acidity), offering valuable insights for the rational design of robust catalysts for NO<i><sub><i>x</i></sub></i> abatement.

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Publication Details

Journal
Inorganic Chemistry
Published
2025-05-06
DOI
https://doi.org/10.1021/acs.inorgchem.5c01039
Citations
2
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
1.04

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article

Insights into the Synergistic Promotion Effect of Cu and W Modification on the Catalytic Performance of α-Fe2O3 for NH3-SCR of NOx

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Insights into the Synergistic Promotion Effect of Cu and W Modification on the Catalytic Performance of α-Fe2O3 for NH3-SCR of NOx

Pengkai Jin, Chengyan Ge, Kaili Ma, Wei Tan, Jingfang Sun, Lin Dong, Qianni Cheng, Wang Song, Yirui Yang, Wanting Yan
article en
2 citations

Abstract

A dual-element modification strategy was proposed to promote the catalytic performance of the α-Fe<sub>2</sub>O<sub>3</sub> catalyst for the selective catalytic reduction of NO<i><sub><i>x</i></sub></i> by NH<sub>3</sub> (NH<sub>3</sub>-SCR of NO<i><sub><i>x</i></sub></i>) at both low and high temperatures. By optimizing the loading amount of CuO (4 wt %) and WO<sub>3</sub> (5 wt %), a wide operating temperature window (150-350 °C) was achieved on the modified α-Fe<sub>2</sub>O<sub>3</sub> catalyst (W<sub>5</sub>/Cu<sub>4</sub>/Fe). Further characterizations revealed that the enhanced low-temperature activity could be attributed to the improved redox performance of α-Fe<sub>2</sub>O<sub>3</sub> through CuO modification, while the superior high-temperature activity was primarily ascribed to the enhanced surface acidity induced by WO<sub>3</sub> modification. The synergistic effect of CuO and WO<sub>3</sub> modifications facilitated the NH<sub>3</sub>-SCR reaction on the modified α-Fe<sub>2</sub>O<sub>3</sub> catalysts to efficiently proceed through the Eley-Rideal (E-R) mechanism pathway. This provided compelling evidence that the catalytic performance of NH<sub>3</sub>-SCR catalysts at different temperatures was dominantly governed by distinct factors (e.g., redox property and surface acidity), offering valuable insights for the rational design of robust catalysts for NO<i><sub><i>x</i></sub></i> abatement.

Inorganic ChemistryVol. 64(19)
State Key Laboratory of Pollution Control and Resource Reuse (CN), Analysis and Testing Centre (CN), Yancheng Institute of Technology (CN), Nanjing University (CN)
China Association for Science and Technology, National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province
Openalex Percentile: Top 26%
Catalytic Processes in Materials Science
1.04
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