Ammonia-Assisted Photosynthesis of Ethylene Glycol

Photocatalytic C-C coupling of methanol provides an appealing approach to producing ethylene glycol (EG) with theoretically zero-carbon cost loss. However, the high polarity of the O-H group severely inhibited the formation and desorption of key radical intermediates, resulting in a low ethylene glycol yield and selectivity. Herein, we report an ammonia-assisted method to promote the efficient photosynthesis of ethylene glycol by amino/ammonia modification on the catalyst surface. After optimization, a 45-fold enhancement of the ethylene glycol production rate (5085 μmol g<sup>-1</sup> h<sup>-1</sup>) and an outstanding rise of carbon selectivity can be obtained (91.1%). As revealed by a series of <i>in situ</i> characterizations, we demonstrate that the hydrogen bond between absorbed methanol and the amino group/ammonia could restrain the preferential oxidation of hydroxyl groups on the catalyst surface, leading to the productive production of key ·CH<sub>2</sub>OH for high-efficiency ethylene glycol photosynthesis. This work demonstrated that nonchemical bonding interactions can effectively modulate radical reaction pathways, thereby enabling high-selectivity photocatalysis.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-11-05
DOI
https://doi.org/10.1021/jacs.5c14704
Citations
1
Primary Topic
Catalysis for Biomass Conversion
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article
Field-Weighted Citation Impact
0.67
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article

Ammonia-Assisted Photosynthesis of Ethylene Glycol

Qian Xi, Tierui Zhang, Junyu Gao, Li‐Zhu Wu et al.
1 citations
Journal of the American Chemical Society
Catalysis for Biomass Conversion
0.67
article

Ammonia-Assisted Photosynthesis of Ethylene Glycol

Qian Xi, Tierui Zhang, Junyu Gao, Li‐Zhu Wu, Yunxuan Zhao, Tao Hu, Lei Kang, Jinhu Wang
article en
1 citations

Abstract

Photocatalytic C-C coupling of methanol provides an appealing approach to producing ethylene glycol (EG) with theoretically zero-carbon cost loss. However, the high polarity of the O-H group severely inhibited the formation and desorption of key radical intermediates, resulting in a low ethylene glycol yield and selectivity. Herein, we report an ammonia-assisted method to promote the efficient photosynthesis of ethylene glycol by amino/ammonia modification on the catalyst surface. After optimization, a 45-fold enhancement of the ethylene glycol production rate (5085 μmol g<sup>-1</sup> h<sup>-1</sup>) and an outstanding rise of carbon selectivity can be obtained (91.1%). As revealed by a series of <i>in situ</i> characterizations, we demonstrate that the hydrogen bond between absorbed methanol and the amino group/ammonia could restrain the preferential oxidation of hydroxyl groups on the catalyst surface, leading to the productive production of key ·CH<sub>2</sub>OH for high-efficiency ethylene glycol photosynthesis. This work demonstrated that nonchemical bonding interactions can effectively modulate radical reaction pathways, thereby enabling high-selectivity photocatalysis.

Journal of the American Chemical SocietyVol. 147(46)
Chinese Academy of Sciences (CN), Technical Institute of Physics and Chemistry (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 25%
Catalysis for Biomass Conversion
0.67
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