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Metal Support Interaction in Pt Nanoparticles Partially Confined in the Mesopores of Microsized Mesoporous CeO2 for Highly Efficient Purification of Volatile Organic Compounds
Abstract
The Pt/CeO 2 nanocomposites of Pt nanoparticles partially confined in the mesopores of microsized mesoporous CeO 2 (1.0% Pt/CeO 2 -MM) or supported on the surface of CeO 2 nanocubes (1.0% Pt/CeO 2 -NC) with the same Pt loading of 1.0 wt % were prepared by the impregnation of microsized mesoporous CeO 2 or CeO 2 nanocubes with Pt(NO 3 ) 2 aqueous solution, followed by the reduction with NaBH 4 aqueous solution. 1.0%Pt/CeO 2 -MM exhibits much higher catalytic activity for benzene oxidation than 1.0%Pt/CeO 2 -NC. Compared to 1.0% Pt/CeO 2 -NC, the reaction temperatures of T 50 and T 90 (corresponding to a benzene conversion = 50% and 90%) for 1.0% Pt/CeO 2 -MM tremendously decreases by Δ T 50 = 149 °C and Δ T 90 = 196 °C, respectively. The turnover frequency (TOF) of 1.0% Pt/CeO 2 -MM at 140 °C increases by 9.0 times as compared to that of 1.0% Pt/CeO 2 -NC. The tremendous enhancement in the catalytic activity is due to a novel metal support interaction in 1.0% Pt/CeO 2 -MM. The novel metal support interaction is theoretically studied by density function theory (DFT) calculation and experimentally studied by CO-TPR, CO-TPD, H 2 pulse titration, and HRTEM. The theoretical and experimental evidence reveal that the partial confinement of Pt nanoparticles in the mesopores of microsized mesoporous CeO 2 leads to a significant enhancement in the activity of the surface lattice oxygen around the interface between Pt nanoparticles and CeO 2, thus tremendously increasing the catalytic activity.
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The surface science of titanium dioxide
Diebold, U. (2003) · Surface Science Reports · doi:10.1016/s0167-5729(02)00100-0 · Cited by 7,944
Bruix, A., Rodriguez, J. A., Ramírez, P. J., Senanayake, S. D., Evans, J., Park, J. B., Stacchiola, D., Liu, P., Hrbek, J., & Illas, F. (2012) · Journal of the American Chemical Society · doi:10.1021/ja302070k · Cited by 839
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Li, X., Yu, J., Jaroniec, M., & Chen, X. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00400 · Cited by 2,304
An, J., Wang, Y., Lu, J., Zhang, J., Zhang, Z., Xu, S., Liu, X., Zhang, T., Gocyla, M., Heggen, M., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b01742 · Cited by 258
Metadata
- Authors
- Mao, M., Lv, H., Li, Y., Yang, Y., Zeng, M., Li, N., & Zhao, X.
- Venue
- ACS Catalysis
- Publisher
- American Chemical Society (ACS)
- Published
- 2015-12-16
- Volume
- 6
- Issue
- 1
- Pages
- 418-427
- ISSN
- 2155-5435 (ISSN-L)
- OpenAlex
- W2338428912
- Cited by
- 166
- References
- 2
- FWCI
- 4.66
- Type
- journal article
- Language
- en
- Open access
- closed
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- Mao, M., Lv, H., Li, Y., Yang, Y., Zeng, M., Li, N., & Zhao, X. (2016). Metal Support Interaction in Pt Nanoparticles Partially Confined in the Mesopores of Microsized Mesoporous CeO2 for Highly Efficient Purification of Volatile Organic Compounds. ACS Catalysis. https://doi.org/10.1021/acscatal.5b02371
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