Single‐Atom Ru Anchored Mesoporous TiO <sub>2</sub> Phase‐Junction Promotes Photocatalytic Biomass Conversion

D Duoxin Shi (College of Energy Materials and Chemistry College of Chemistry and Chemical Engineering Inner Mongolia University Hohhot 010070 China) J Jiaming Zhang (College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering) Z Zheng Qi L Linlin Duan (College of Chemistry and Materials, Department of Chemistry, Laboratory of Advanced Materials) R Ruohan Yu (Wuhan University of Technology the Sanya Science and Education Innovation) Q Qin Yue (Institute of Fundamental and Frontier Sciences) D Di Meng T Tianke Kang L Linjie Liu K Kun Lan (College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering) W Wei Li D Dongyuan Zhao (Laboratory of Advanced Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion, Fudan University, 220 Handan, Shanghai 200433, P. R. China) L Limin Wu (School of Chemistry and Chemical Engineering) Y Yuzhu Ma (College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering)

Abstract

Abstract Constructing advanced semiconductor nanoreactors is an effective route to boost the efficient photocatalytic conversion of biomasses to high‐value‐added products. Herein, single‐atom anchored flower‐like mesoporous TiO 2 nanoreactors with tunable anatase‐rutile crystalline phases are prepared via a micelle‐interface confined co‐assembly strategy (Ru 0.5 /A&amp;R‐TNs). This approach not only facilitates the introduction of various monatomic/diatomic (e.g., Ru, Mo, Pd, Pt, etc.) sites but also spontaneously induces the TiO 2 phase transformation from anatase to rutile, achieving precise control of two‐phase ratios. The interface of the two phases with abundant oxygen vacancies (O v ) facilitates the adsorption and activation of 5‐hydroxymethylfurfural (HMF), which exhibits a high photocatalytic HMF oxidation to DFF (selectivity of 90.8%). Based on the optimal phase compositions, the doping of Ru single‐atom further exhibits a high atom utilization and suitable electronic structure. Therefore, the Ru 0.5 /A&amp;R‐TNs achieve the cascade conversion from HMF to 5‐formyl‐2‐furoic acid with a selectivity of 75.8%. This research provides innovative ways for single‐atom catalyst synthesis, and the mechanism of synergistic catalytic action may provide new guidance for the photocatalytic conversion of high‐value‐added products from HMF.

Article Details

Volume / Issue Vol. 37, Issue 38
Published September 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

D

Duoxin Shi

College of Energy Materials and Chemistry College of Chemistry and Chemical Engineering Inner Mongolia University Hohhot 010070 China

J

Jiaming Zhang

College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering

Z

Zheng Qi

L

Linlin Duan

College of Chemistry and Materials, Department of Chemistry, Laboratory of Advanced Materials

R

Ruohan Yu

Wuhan University of Technology the Sanya Science and Education Innovation

Q

Qin Yue

Institute of Fundamental and Frontier Sciences

D

Di Meng

T

Tianke Kang

L

Linjie Liu

K

Kun Lan

College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering

W

Wei Li

D

Dongyuan Zhao

Laboratory of Advanced Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion, Fudan University, 220 Handan, Shanghai 200433, P. R. China

L

Limin Wu

School of Chemistry and Chemical Engineering

Y

Yuzhu Ma

College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering