Efficient electrochemical production of glucaric acid and H2 via glucose electrolysis

Glucose electrolysis offers a prospect of value-added glucaric acid synthesis and energy-saving hydrogen production from the biomass-based platform molecules. Here we report that nanostructured NiFe oxide (NiFeO x ) and nitride (NiFeN x ) catalysts, synthesized from NiFe layered double hydroxide nan...

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Published inNature communications Vol. 11; no. 1; pp. 265 - 11
Main Authors Liu, Wu-Jun, Xu, Zhuoran, Zhao, Dongting, Pan, Xiao-Qiang, Li, Hong-Chao, Hu, Xiao, Fan, Zhi-Yong, Wang, Wei-Kang, Zhao, Guo-Hua, Jin, Song, Huber, George W., Yu, Han-Qing
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 14.01.2020
Nature Publishing Group
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Summary:Glucose electrolysis offers a prospect of value-added glucaric acid synthesis and energy-saving hydrogen production from the biomass-based platform molecules. Here we report that nanostructured NiFe oxide (NiFeO x ) and nitride (NiFeN x ) catalysts, synthesized from NiFe layered double hydroxide nanosheet arrays on three-dimensional Ni foams, demonstrate a high activity and selectivity towards anodic glucose oxidation. The electrolytic cell assembled with these two catalysts can deliver 100 mA cm −2 at 1.39 V. A faradaic efficiency of 87% and glucaric acid yield of 83% are obtained from the glucose electrolysis, which takes place via a guluronic acid pathway evidenced by in-situ infrared spectroscopy. A rigorous process model combined with a techno-economic analysis shows that the electrochemical reduction of glucose produces glucaric acid at a 54% lower cost than the current chemical approach. This work suggests that glucose electrolysis is an energy-saving and cost-effective approach for H 2 production and biomass valorization. Renewable biomass conversion may afford high-value products from common materials, but catalysts usually require expensive metals and exhibit poor selectivities. Here, authors employ nickel-iron oxide and nitride electrocatalysts to produce H 2 and to convert glucose to glucaric acid selectively.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-14157-3