Shen, Xiaoqiang

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26ba01ba-6772-4c17-917e-5b46a7b1899d
  • Shen, Xiaoqiang (2)
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Author's Bibliography

Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts

Tang, Tian; Ye, Lyumeng; Chen, Yanrong; Xue, Jingyu; Shen, Xiaoqiang; Chen, Jinfei; Quarcoo, Fiona Hammond; Rac, Vladislav; Rakić, Vesna; Li, Xinbao; Du, Xuesen

(2024)

TY  - JOUR
AU  - Tang, Tian
AU  - Ye, Lyumeng
AU  - Chen, Yanrong
AU  - Xue, Jingyu
AU  - Shen, Xiaoqiang
AU  - Chen, Jinfei
AU  - Quarcoo, Fiona Hammond
AU  - Rac, Vladislav
AU  - Rakić, Vesna
AU  - Li, Xinbao
AU  - Du, Xuesen
PY  - 2024
UR  - https://www.sciencedirect.com/science/article/pii/S0926337323010111
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/6464
AB  - The unique interface synergistic catalytic properties for metal oxide-supported catalysts have long been explored in several critical heterogeneous catalytic processes (e.g., CO oxidation reactions). However, interfacial synergistic catalysis is still a hitherto undescribed mechanism due to the lack of direct evidence at the atomic level. Thereinto, the CuOx-supported CeO2 (CuOx/CeO2) catalyst is a typical case. Herein, a combination study including representative theoretical calculations, in situ DRIFTS spectra and tailored molecular probe experiments supports a new carbonate-interface mediated Mars-van Krevelen (M−vK) mechanism for CO oxidation, i.e., CO molecules form carbonate intermediate species directly between spatial proximity (2.99 Å) double lattice oxygen sites with low oxygen vacancies formation energy (EformOv = 0.82 eV/0.83 eV) at the copper−ceria interface. The reaction energy barrier of this process is 0.32 eV, much lower than the 1.23 eV of the conventional M−vK mechanism. Besides, the spatial effect of double oxygen vacancies (Ov) generated by the depletion of intermediate carbonate species promotes the sustained and dynamic activation of O2, hence facilitating the efficient operation of the M−vK mechanism at low temperatures.
T2  - Applied Catalysis B: Environmental
T2  - Applied Catalysis B: EnvironmentalApplied Catalysis B: Environmental
T1  - Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts
SP  - 123368
VL  - 342
DO  - 10.1016/j.apcatb.2023.123368
ER  - 
@article{
author = "Tang, Tian and Ye, Lyumeng and Chen, Yanrong and Xue, Jingyu and Shen, Xiaoqiang and Chen, Jinfei and Quarcoo, Fiona Hammond and Rac, Vladislav and Rakić, Vesna and Li, Xinbao and Du, Xuesen",
year = "2024",
abstract = "The unique interface synergistic catalytic properties for metal oxide-supported catalysts have long been explored in several critical heterogeneous catalytic processes (e.g., CO oxidation reactions). However, interfacial synergistic catalysis is still a hitherto undescribed mechanism due to the lack of direct evidence at the atomic level. Thereinto, the CuOx-supported CeO2 (CuOx/CeO2) catalyst is a typical case. Herein, a combination study including representative theoretical calculations, in situ DRIFTS spectra and tailored molecular probe experiments supports a new carbonate-interface mediated Mars-van Krevelen (M−vK) mechanism for CO oxidation, i.e., CO molecules form carbonate intermediate species directly between spatial proximity (2.99 Å) double lattice oxygen sites with low oxygen vacancies formation energy (EformOv = 0.82 eV/0.83 eV) at the copper−ceria interface. The reaction energy barrier of this process is 0.32 eV, much lower than the 1.23 eV of the conventional M−vK mechanism. Besides, the spatial effect of double oxygen vacancies (Ov) generated by the depletion of intermediate carbonate species promotes the sustained and dynamic activation of O2, hence facilitating the efficient operation of the M−vK mechanism at low temperatures.",
journal = "Applied Catalysis B: Environmental, Applied Catalysis B: EnvironmentalApplied Catalysis B: Environmental",
title = "Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts",
pages = "123368",
volume = "342",
doi = "10.1016/j.apcatb.2023.123368"
}
Tang, T., Ye, L., Chen, Y., Xue, J., Shen, X., Chen, J., Quarcoo, F. H., Rac, V., Rakić, V., Li, X.,& Du, X.. (2024). Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts. in Applied Catalysis B: Environmental, 342, 123368.
https://doi.org/10.1016/j.apcatb.2023.123368
Tang T, Ye L, Chen Y, Xue J, Shen X, Chen J, Quarcoo FH, Rac V, Rakić V, Li X, Du X. Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts. in Applied Catalysis B: Environmental. 2024;342:123368.
doi:10.1016/j.apcatb.2023.123368 .
Tang, Tian, Ye, Lyumeng, Chen, Yanrong, Xue, Jingyu, Shen, Xiaoqiang, Chen, Jinfei, Quarcoo, Fiona Hammond, Rac, Vladislav, Rakić, Vesna, Li, Xinbao, Du, Xuesen, "Diving into the interface-mediated Mars-van Krevelen (M−vK) characteristic of CuOx-supported CeO2 catalysts" in Applied Catalysis B: Environmental, 342 (2024):123368,
https://doi.org/10.1016/j.apcatb.2023.123368 . .
3

Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species

Wan, Yuyi; Yang, Guangpeng; Xiang, Jinyao; Shen, Xiaoqiang; Yang, Dafei; Chen, Yanrong; Rac, Vladislav; Rakić, Vesna; Du, Xuesen

(Royal Soc Chemistry, Cambridge, 2020)

TY  - JOUR
AU  - Wan, Yuyi
AU  - Yang, Guangpeng
AU  - Xiang, Jinyao
AU  - Shen, Xiaoqiang
AU  - Yang, Dafei
AU  - Chen, Yanrong
AU  - Rac, Vladislav
AU  - Rakić, Vesna
AU  - Du, Xuesen
PY  - 2020
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5328
AB  - Cu-SAPO-34 catalysts with varied Cu loadings were synthesized through ion exchange to study the influence of water on the NH3-SCR reaction. The catalytic activities were evaluated by selective catalytic reduction of NO under a reactant feed in the presence/absence of water. Transient experiments were designed to study the response of NO conversion to the presence of water. H-2-TPR and DFT calculations were performed to study the reducibility of Cu species. NH3-TPD and XPS were conducted to reveal the migration of Cu species. The results show that water could remarkably improve NO reduction activities and the promoting effect is more significant on the catalyst with low Cu loading. Both transient and permanent influences were found in this promoting phenomenon. For the transient influence, water has been proved to accelerate the re-oxidation half-cycle. Moreover, water can enhance the promoting effect of the SCR feed on the migration of Cu species. These unanchored Cu ions migrate to defect sites to form active sites, which lead to a permanent influence of water.
PB  - Royal Soc Chemistry, Cambridge
T2  - Dalton Transactions
T1  - Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species
EP  - 773
IS  - 3
SP  - 764
VL  - 49
DO  - 10.1039/c9dt03848e
ER  - 
@article{
author = "Wan, Yuyi and Yang, Guangpeng and Xiang, Jinyao and Shen, Xiaoqiang and Yang, Dafei and Chen, Yanrong and Rac, Vladislav and Rakić, Vesna and Du, Xuesen",
year = "2020",
abstract = "Cu-SAPO-34 catalysts with varied Cu loadings were synthesized through ion exchange to study the influence of water on the NH3-SCR reaction. The catalytic activities were evaluated by selective catalytic reduction of NO under a reactant feed in the presence/absence of water. Transient experiments were designed to study the response of NO conversion to the presence of water. H-2-TPR and DFT calculations were performed to study the reducibility of Cu species. NH3-TPD and XPS were conducted to reveal the migration of Cu species. The results show that water could remarkably improve NO reduction activities and the promoting effect is more significant on the catalyst with low Cu loading. Both transient and permanent influences were found in this promoting phenomenon. For the transient influence, water has been proved to accelerate the re-oxidation half-cycle. Moreover, water can enhance the promoting effect of the SCR feed on the migration of Cu species. These unanchored Cu ions migrate to defect sites to form active sites, which lead to a permanent influence of water.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Dalton Transactions",
title = "Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species",
pages = "773-764",
number = "3",
volume = "49",
doi = "10.1039/c9dt03848e"
}
Wan, Y., Yang, G., Xiang, J., Shen, X., Yang, D., Chen, Y., Rac, V., Rakić, V.,& Du, X.. (2020). Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species. in Dalton Transactions
Royal Soc Chemistry, Cambridge., 49(3), 764-773.
https://doi.org/10.1039/c9dt03848e
Wan Y, Yang G, Xiang J, Shen X, Yang D, Chen Y, Rac V, Rakić V, Du X. Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species. in Dalton Transactions. 2020;49(3):764-773.
doi:10.1039/c9dt03848e .
Wan, Yuyi, Yang, Guangpeng, Xiang, Jinyao, Shen, Xiaoqiang, Yang, Dafei, Chen, Yanrong, Rac, Vladislav, Rakić, Vesna, Du, Xuesen, "Promoting effects of water on the NH3-SCR reaction over Cu-SAPO-34 catalysts: transient and permanent influences on Cu species" in Dalton Transactions, 49, no. 3 (2020):764-773,
https://doi.org/10.1039/c9dt03848e . .
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