TY - JOUR
T1 - Electrosynthesis of ethylene glycol from C1 feedstocks in a flow electrolyzer
AU - Xia, Rong
AU - Wang, Ruoyu
AU - Hasa, Bjorn
AU - Lee, Ahryeon
AU - Liu, Yuanyue
AU - Ma, Xinbin
AU - Jiao, Feng
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Ethylene glycol is a widely utilized commodity chemical, the production of which accounts for over 46 million tons of CO2 emission annually. Here we report a paired electrocatalytic approach for ethylene glycol production from methanol. Carbon catalysts are effective in reducing formaldehyde into ethylene glycol with a 92% Faradaic efficiency, whereas Pt catalysts at the anode enable formaldehyde production through methanol partial oxidation with a 75% Faradaic efficiency. With a membrane-electrode assembly configuration, we show the feasibility of ethylene glycol electrosynthesis from methanol in a single electrolyzer. The electrolyzer operates a full cell voltage of 3.2 V at a current density of 100 mA cm−2, with a 60% reduction in energy consumption. Further investigations, using operando flow electrolyzer mass spectroscopy, isotopic labeling, and density functional theory (DFT) calculations, indicate that the desorption of a *CH2OH intermediate is the crucial step in determining the selectively towards ethylene glycol over methanol.
AB - Ethylene glycol is a widely utilized commodity chemical, the production of which accounts for over 46 million tons of CO2 emission annually. Here we report a paired electrocatalytic approach for ethylene glycol production from methanol. Carbon catalysts are effective in reducing formaldehyde into ethylene glycol with a 92% Faradaic efficiency, whereas Pt catalysts at the anode enable formaldehyde production through methanol partial oxidation with a 75% Faradaic efficiency. With a membrane-electrode assembly configuration, we show the feasibility of ethylene glycol electrosynthesis from methanol in a single electrolyzer. The electrolyzer operates a full cell voltage of 3.2 V at a current density of 100 mA cm−2, with a 60% reduction in energy consumption. Further investigations, using operando flow electrolyzer mass spectroscopy, isotopic labeling, and density functional theory (DFT) calculations, indicate that the desorption of a *CH2OH intermediate is the crucial step in determining the selectively towards ethylene glycol over methanol.
UR - http://www.scopus.com/inward/record.url?scp=85165958301&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-40296-9
DO - 10.1038/s41467-023-40296-9
M3 - Article
C2 - 37516779
AN - SCOPUS:85165958301
SN - 2041-1723
VL - 14
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 4570
ER -