Author
Listed:
- Yan Lin
(China University of Petroleum (East China)
Tsinghua University)
- Hui Li
(China University of Petroleum (East China))
- Xiaodong Miao
(China University of Petroleum (East China))
- Yunayuan Sun
(China University of Petroleum (East China))
- Hao Ren
(China University of Petroleum (East China))
- Xifeng Yu
(China University of Petroleum (East China))
- Wangyang Cui
(China University of Petroleum (East China))
- Mingbo Wu
(China University of Petroleum (East China))
- Zhongtao Li
(China University of Petroleum (East China))
Abstract
Direct electro-epoxidation of propylene (D-EOPO) with a membrane electrode assembly (MEA) system represents a sustainable approach for producing propylene oxide, which can reduce ohmic losses and simplify product separation. To address the challenges of selectivity and activity, we develop an Ag/V catalyst and integrate it into the “liquid-free” MEA reactor for continues D-EOPO. The V in the catalyst facilitates the formation of Ag-O active centers, thereby reducing the generation energy of *O radicals. Meanwhile, V doping also results in a downshift of the d-band center of the Ag sites. Consequently, the formation of the crucial intermediate (*OC3H6) is significantly accelerated through the coupling *O with adsorbed propylene, thereby markedly improving propylene oxide (PO) production. The MEA reactor, integrated with the developed Ag/V catalyst, can maintain a stable production rate of PO at 227 μmol/h over a period of 78 hours. Thus, the “liquid-free” electro-epoxidation protocol developed here exhibits greater industrial applicability.
Suggested Citation
Yan Lin & Hui Li & Xiaodong Miao & Yunayuan Sun & Hao Ren & Xifeng Yu & Wangyang Cui & Mingbo Wu & Zhongtao Li, 2025.
"V activated electro-epoxidation catalyst in membrane electrode assembly system for the production of propylene oxide,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58486-y
DOI: 10.1038/s41467-025-58486-y
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