4.8 Article

Modulating the Energy Band to Inhibit the Over-oxidation for Highly Selective Anisaldehyde Production Coupled with Robust H2 Evolution from Water Splitting

Journal

ACS CATALYSIS
Volume 11, Issue 14, Pages 8727-8735

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c01520

Keywords

photocatalytic coupled reaction; anisaldehyde production; H-2 evolution; high selectivity

Funding

  1. National Key R&D Program of China [2020YFA0710404]
  2. Beijing Natural Science Foundation [2182077]
  3. National Natural Science Foundation of China [21477136]

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The study introduces a novel photocatalytic method using specific type-II heterojunction photocatalysts to achieve selective conversion of aromatic alcohols to aldehydes and generate H-2 in pure water, with high efficiency and selectivity.
Aromatic aldehydes are important precursors for pharmaceutical, agricultural, and synthetic chemistry. Compared to thermal catalysis and organic solvent synthesis systems, photocatalytic selective conversion of aromatic alcohol to the corresponding aldehyde coupled with H-2 evolution in pure water represents an alternative due to the mild reaction conditions and the renewable energy production. However, this coupling reaction in aqueous solution is still limited by the low selectivity and conversion due to the over-oxidation. Herein, we demonstrated that the typical type-II heterojunction photocatalysts with a moderate energy band can restrain over-oxidation. This strategy effectively separates the photoexcited charge and hampers the complicated radical oxidation process, thus favoring the generation of aldehyde with the robust evolution of H-2 under visible light illumination without any cocatalyst. The system realizes an anisaldehyde (AA) selectivity of over 99% and a 4-methoxybenzyl alcohol (4-MBA) conversion of over 99% in a low concentration of 4-MBA. Furthermore, when the amount of 4-MBA is expanded to the mL level, the system is able to maintain a robust H-2 evolution rate of 291.8 mmol.g(-1).h(-1) at over 99% selectivity for AA. Mechanistic investigation reveals that the photoexcited hole with a moderate potential directly reacts with 4-MBA by promoting the formation of a benzyl carbon radical with abstraction of a hydrogen atom due to the inhibition of (OH)-O-center dot formation. Moreover, the effective contact between water, photocatalysts, and 4-MBA also contributes to enhance the conversion activity and improve the practical application potential. The method can be further extended to various aromatic alcohols and offers a concept for highly selective synthesis of high-added value chemicals coupled with H-2 evolution in pure water.

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