Heterolytic Hydrogenation and H<sup>–</sup> Migration-Assisted Hydrodeoxygenation Reaction under Mild Conditions over Pt/TiO<sub>2</sub>-D

Hydrodeoxygenation of lignin-derived guaiacol to aromatic products under mild conditions was achieved using an interesting Pt/TiO2-D catalyst. The defects in TiO2-D played a pivotal role in H2 dissociation and exhibited a unique capability for the migration of active H species on the surface and within the bulk phase of TiO2-D, resulting in the formation of a “H reservoir” adjacent to the Pt active sites. Consequently, Pt/TiO2-D exhibited superb activity for the cleavage of the C–O bond under extremely low hydrogen concentration (1 atm 10% H2/Ar). Moreover, the H−migration into the TiO2-D bulk induced the formation of a new Ti3O5 crystalline phase, creating additional defects, which in turn accelerated H2 activation, the formation of Pt-H species, and the H reservoir, which account for the satisfactory ability of Pt/TiO2-D for guaiacol adsorption and C–O cleavage under mild conditions.

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Publication Details

Journal
ACS Catalysis
Published
2024-09-03
DOI
https://doi.org/10.1021/acscatal.4c04196
Citations
39
Primary Topic
Catalysis and Hydrodesulfurization Studies
Type
article
Field-Weighted Citation Impact
8.29

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article

Heterolytic Hydrogenation and H– Migration-Assisted Hydrodeoxygenation Reaction under Mild Conditions over Pt/TiO2-D

Fengyu Zhao, Chao Zhang, Tingting Xiao, Xinchao Wang et al.
39 citations
ACS Catalysis
Catalysis and Hydrodesulfurization Studies
8.29
article

Heterolytic Hydrogenation and H– Migration-Assisted Hydrodeoxygenation Reaction under Mild Conditions over Pt/TiO2-D

Fengyu Zhao, Chao Zhang, Tingting Xiao, Xinchao Wang, Yanchun Liu
article en
39 citations

Abstract

Hydrodeoxygenation of lignin-derived guaiacol to aromatic products under mild conditions was achieved using an interesting Pt/TiO2-D catalyst. The defects in TiO2-D played a pivotal role in H2 dissociation and exhibited a unique capability for the migration of active H species on the surface and within the bulk phase of TiO2-D, resulting in the formation of a “H reservoir” adjacent to the Pt active sites. Consequently, Pt/TiO2-D exhibited superb activity for the cleavage of the C–O bond under extremely low hydrogen concentration (1 atm 10% H2/Ar). Moreover, the H−migration into the TiO2-D bulk induced the formation of a new Ti3O5 crystalline phase, creating additional defects, which in turn accelerated H2 activation, the formation of Pt-H species, and the H reservoir, which account for the satisfactory ability of Pt/TiO2-D for guaiacol adsorption and C–O cleavage under mild conditions.

ACS CatalysisVol. 14(18)
University of Science and Technology of China (CN), Northeast Normal University (CN), Chinese Academy of Sciences (CN), Changchun Institute of Applied Chemistry (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 1%
Catalysis and Hydrodesulfurization Studies
8.29
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Heterolytic Hydrogenation and H<sup>–</sup> Migration-Assisted Hydrodeoxygenation Reaction under Mild Conditions over Pt/TiO<sub>2</sub>-D — Fengyu Zhao, Chao Zhang, et al. · ACS Catalysis (2024) | TGRS Research Map | TGRS