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March 7, 2026Journal of the American Chemical Society5 citations

Efficient and Selective Hydroxyl-Mediated Photocatalytic Ethane Oxidation to Acetic Acid

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SYSiyuan YangGZGuangyao ZhaiJXJunchi Xu

Key Points

  • The research aims to develop an efficient strategy for converting ethane into acetic acid using photocatalytic methods.
  • Utilized a photocatalytic system combining Pd nanoparticles and titanium dioxide nanocrystals.
  • Promoted the generation of hydroxyl radicals to activate C(sp3)-H bonds.
  • Operated under mild temperature conditions with light illumination.
  • Achieved acetic acid productivity of approximately 5.65 mmol g<sub>photocatalyst</sub><sup>-1</sup> h<sup>-1</sup>.
  • Produced an acetic acid concentration of around 40 mM in 102 hours.
  • Maintained close to 100% selectivity for acetic acid in liquid phase products.

Abstract

Ethane offers a promising feedstock for sustainable acetic acid production. However, the chemical inertness of ethane and the multiple ethane oxidation steps greatly restrict the acetic acid productivity and selectivity. In this work, we report a photocatalytic strategy that promotes the generation of •OH to accelerate C (sp3) -H bond activation while steering sequential ethane oxidation to produce acetic acid. Our approach leverages spatially decoupled photoredox sites by integrating Pd nanoparticles onto titanium dioxide nanocrystals with mainly exposed 001 facets, enabling synergistic activation of molecular oxygen and water for enhanced •OH generation under mild conditions. This photocatalytic system achieves an acetic acid productivity of ∼5. 65 mmol gphotocatalyst-1 h-1, producing an aqueous acetic acid solution of ∼40 mM in 102 h under light illumination with close to 100% acetic acid selectivity in liquid phase products. Our findings establish an efficient approach for selective alkane valorization to synthesize value-added chemicals at ambient temperature.

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Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/69abc2175af8044f7a4eb630https://doi.org/10.1021/jacs.5c21702
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