Inverse decoration of TiOx to NiSn alloy nanoparticles for efficient hydrodeoxygenation of m-cresol

Hydrodeoxygenation (HDO) of phenolics is crucial for lignin-to-fuel production via fast pyrolysis. The reaction under atmospheric H<sub>2</sub> pressure offers compatibility with pyrolysis conditions, high aromatic selectivity and low H<sub>2</sub> consumption, but suffers from coking-induced catalyst deactivation. In this work, we report a TiO<sub>x</sub>-decorated NiSn/SiO<sub>2</sub> catalyst (Ti-NiSn/SiO<sub>2</sub>), achieving 100% deoxygenation selectivity and enhanced stability in m-cresol HDO. The superior performance stems from: (i) the interfacial synergy between TiO<sub>x</sub> and NiSn alloy that facilitates C-O bond cleavage with a reduced energy barrier; (ii) the geometric isolation and electron-donating properties of Sn, which suppress undesirable side reactions and mitigate coke formation; and (iii) the inverse TiO<sub>x</sub> decoration strategy, which enables effective interface chemistry while minimizing acidic sites that could otherwise accelerate coking. This study presents a design strategy for constructing inverse oxide-alloy interface catalysts, offering multi-faceted advantages for HDO and other complex catalytic transformations.

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Journal
Nature Communications
Published
2025-12-19
DOI
https://doi.org/10.1038/s41467-025-67624-5
Primary Topic
Catalysis and Hydrodesulfurization Studies
Type
article
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article

Inverse decoration of TiOx to NiSn alloy nanoparticles for efficient hydrodeoxygenation of m-cresol

Yaowen Xu, Shixiang Yu, Maolin Wang, Ding Ma et al.
Nature Communications
Catalysis and Hydrodesulfurization Studies
article

Inverse decoration of TiOx to NiSn alloy nanoparticles for efficient hydrodeoxygenation of m-cresol

Yaowen Xu, Shixiang Yu, Maolin Wang, Ding Ma, Xiaodong Yi, Chengyu Li, Jiankang Zhao, Feifei Yang, Wei Zhou
article en

Abstract

Hydrodeoxygenation (HDO) of phenolics is crucial for lignin-to-fuel production via fast pyrolysis. The reaction under atmospheric H<sub>2</sub> pressure offers compatibility with pyrolysis conditions, high aromatic selectivity and low H<sub>2</sub> consumption, but suffers from coking-induced catalyst deactivation. In this work, we report a TiO<sub>x</sub>-decorated NiSn/SiO<sub>2</sub> catalyst (Ti-NiSn/SiO<sub>2</sub>), achieving 100% deoxygenation selectivity and enhanced stability in m-cresol HDO. The superior performance stems from: (i) the interfacial synergy between TiO<sub>x</sub> and NiSn alloy that facilitates C-O bond cleavage with a reduced energy barrier; (ii) the geometric isolation and electron-donating properties of Sn, which suppress undesirable side reactions and mitigate coke formation; and (iii) the inverse TiO<sub>x</sub> decoration strategy, which enables effective interface chemistry while minimizing acidic sites that could otherwise accelerate coking. This study presents a design strategy for constructing inverse oxide-alloy interface catalysts, offering multi-faceted advantages for HDO and other complex catalytic transformations.

Nature CommunicationsVol. 17(1)
University of Science and Technology of China (CN), Xiamen University (CN), Peking University (CN), China University of Mining and Technology (CN), Hefei National Center for Physical Sciences at Nanoscale (CN), Beijing National Laboratory for Molecular Sciences (CN)
Tencent, Beijing Synchrotron Radiation Facility
Openalex Percentile: Top 58%
Catalysis and Hydrodesulfurization Studies
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