Dual‐Emulsifier Coated Photocatalyst for H <sub>2</sub> O <sub>2</sub> Synthesis in Emulsion via Water Oxidation

Photocatalysis provides a sustainable approach for on-site production of H<sub>2</sub>O<sub>2</sub>, yet single-phase systems generally display unsatisfactory efficiency and low concentration of H<sub>2</sub>O<sub>2</sub> due to rapid reverse reactions and dissociation of H<sub>2</sub>O<sub>2</sub>. Multiphase systems are developed to yield aqueous H<sub>2</sub>O<sub>2</sub> via oxygen reduction by employing hydrophobic photocatalysts, however, the low solubility of oxygen and the possible dissociation of generated H<sub>2</sub>O<sub>2</sub> result in a limited improvement in catalytic performances. Herein, a lauric acid (LA)‒n-dodecyltrimethoxysilane (DTMS) dual-emulsifier coated Pd/TiO<sub>2</sub> (LD-Pd/TiO<sub>2</sub>) is constructed for the synthesis of H<sub>2</sub>O<sub>2</sub> in a water-nonane system via water oxidation with quintozene as an insoluble hydrogen acceptor in water. While DTMS in the composite coating quenches the decomposition of H<sub>2</sub>O<sub>2</sub>, LA facilitates the enrichment of quintozene near the Pd/TiO<sub>2</sub> for a rapid consumption of hydrogen atoms. The LD-Pd/TiO<sub>2</sub> leads to a remarkable H<sub>2</sub>O<sub>2</sub> concentration of 133 mM with decent stability and a high quantum efficiency (6.5% at 365 nm). Additionally, the system can be demulsified gently after reaction, obtaining aqueous H<sub>2</sub>O<sub>2</sub> solution and oil phase with hydrogenated products for simple separation and collection.

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Publication Details

Journal
Advanced Science
Published
2025-10-28
DOI
https://doi.org/10.1002/advs.202517645
Citations
1
Primary Topic
TiO2 Photocatalysis and Solar Cells
Type
article
Field-Weighted Citation Impact
0.36

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article

Dual‐Emulsifier Coated Photocatalyst for H 2 O 2 Synthesis in Emulsion via Water Oxidation

Xueyang Leng, Yanbin Shen, Wujun Zhang, Ren Su et al.
1 citations
Advanced Science
TiO2 Photocatalysis and Solar Cells
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article

Dual‐Emulsifier Coated Photocatalyst for H 2 O 2 Synthesis in Emulsion via Water Oxidation

Xueyang Leng, Yanbin Shen, Wujun Zhang, Ren Su, Hong Gao, Emma Richards, Lingling Xu, Flemming Besenbacher, Yuanwei Lu
article en
1 citations

Abstract

Photocatalysis provides a sustainable approach for on-site production of H<sub>2</sub>O<sub>2</sub>, yet single-phase systems generally display unsatisfactory efficiency and low concentration of H<sub>2</sub>O<sub>2</sub> due to rapid reverse reactions and dissociation of H<sub>2</sub>O<sub>2</sub>. Multiphase systems are developed to yield aqueous H<sub>2</sub>O<sub>2</sub> via oxygen reduction by employing hydrophobic photocatalysts, however, the low solubility of oxygen and the possible dissociation of generated H<sub>2</sub>O<sub>2</sub> result in a limited improvement in catalytic performances. Herein, a lauric acid (LA)‒n-dodecyltrimethoxysilane (DTMS) dual-emulsifier coated Pd/TiO<sub>2</sub> (LD-Pd/TiO<sub>2</sub>) is constructed for the synthesis of H<sub>2</sub>O<sub>2</sub> in a water-nonane system via water oxidation with quintozene as an insoluble hydrogen acceptor in water. While DTMS in the composite coating quenches the decomposition of H<sub>2</sub>O<sub>2</sub>, LA facilitates the enrichment of quintozene near the Pd/TiO<sub>2</sub> for a rapid consumption of hydrogen atoms. The LD-Pd/TiO<sub>2</sub> leads to a remarkable H<sub>2</sub>O<sub>2</sub> concentration of 133 mM with decent stability and a high quantum efficiency (6.5% at 365 nm). Additionally, the system can be demulsified gently after reaction, obtaining aqueous H<sub>2</sub>O<sub>2</sub> solution and oil phase with hydrogenated products for simple separation and collection.

Advanced ScienceVol. 13(3)
Harbin Normal University (CN), Chinese Academy of Sciences (CN), Aarhus University (DK), Soochow University (CN), Suzhou Institute of Nano-tech and Nano-bionics (CN), Cardiff University (GB)
Leverhulme Trust, National Natural Science Foundation of China
Openalex Percentile: Top 37%
TiO2 Photocatalysis and Solar Cells
0.36
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