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.
Authors
- Qian Xi (ORCID: https://orcid.org/0000-0002-4119-2913)
- Tierui Zhang (ORCID: https://orcid.org/0000-0002-7948-9413)
- Junyu Gao (ORCID: https://orcid.org/0000-0002-1340-443X)
- Li‐Zhu Wu (ORCID: https://orcid.org/0000-0002-5561-9922)
- Yunxuan Zhao (ORCID: https://orcid.org/0009-0009-0538-2873)
- Tao Hu (ORCID: https://orcid.org/0000-0002-0889-4841)
- Lei Kang (ORCID: https://orcid.org/0000-0002-9993-6399)
- Jinhu Wang (ORCID: https://orcid.org/0000-0002-9061-8634)
Institutions
- Chinese Academy of Sciences (CN)
- Technical Institute of Physics and Chemistry (CN)
- University of Chinese Academy of Sciences (CN)
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
- Type
- article
- Field-Weighted Citation Impact
- 0.67