Energy‐Efficient, Sustainable Cascade Glucose Electrooxidation into Glucaric Acid

M Mingming He C Chao Huang M Mingzi Sun (Department of Chemistry) R Ruixuan Wang Y Yun Song J Jianjun Su (Department of Chemistry and State Key Laboratory of Marine Environmental Health) W Weihua Guo Y Yinger Xin (Department of Chemistry and State Key Laboratory of Marine Environmental Health) Q Qiang Zhang Y Yong Liu G Geng Li (Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China) Z Zihao Li (State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering) R Rui Xue B Bolong Huang (Department of Chemistry) B Ben Zhong Tang (School of Science and Engineering, Guangdong Basic Research Center of Excellence for Aggregate Science, The Chinese University of Hong Kong (Shenzhen), Longgang, Shenzhen 518172, Guangdong, P. R. China) R Ruquan Ye (Department of Chemistry and State Key Laboratory of Marine Environmental Health)

Abstract

ABSTRACT Glucaric acid (GRA) is a critical platform chemical for manufacturing biodegradable materials. Selective glucose (GLU) electrooxidation into GRA provides a sustainable route for biomass valorization. However, conventional methods suffer from energy‐intensive processes due to excessive operational potential exceeding 1.2 V. Here we demonstrate an energy‐efficient tandem system that decouples GRA electrosynthesis into cascade GLU‐to‐gluconic acid (GNA) and GNA‐to‐GRA oxidation. When pairing an Au/C catalyst for selective aldehyde oxidation and an AuPt/C catalyst for hydroxyl oxidation, we achieve 91.8% Faradaic efficiency and nearly 100% conversion efficiency at 0.6 V RHE for GLU‐to‐GNA oxidation, and 81% Faradaic efficiency and 90% conversion efficiency at 0.55 V RHE for GNA‐to‐GRA oxidation. Chronoamperometry demonstrates ∼100% substrate conversion with a minor decrease in product selectivity, confirming the catalyst's excellent stability. Our tandem system improves the overall GLU‐to‐GRA energy efficiency from 13.8% for conventional one‐step route to 31.8%. When oxygen reduction is selected as paired reaction, our system not only enables efficient chemical electrosynthesis, but is also estimated to generate electricity of 1.24 × 10 5  kWh per kiloton GRA, outperforming traditional method with energy consumption of 4.31 × 10 5  kWh. Our work establishes a sustainable and economically viable pathway for biomass valorization, offering a blueprint for circular, carbon‐neutral chemical production.

Article Details

Volume / Issue Vol. 38, Issue 10
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

M

Mingming He

C

Chao Huang

M

Mingzi Sun

Department of Chemistry

R

Ruixuan Wang

Y

Yun Song

J

Jianjun Su

Department of Chemistry and State Key Laboratory of Marine Environmental Health

W

Weihua Guo

Y

Yinger Xin

Department of Chemistry and State Key Laboratory of Marine Environmental Health

Q

Qiang Zhang

Y

Yong Liu

G

Geng Li

Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China

Z

Zihao Li

State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering

R

Rui Xue

B

Bolong Huang

Department of Chemistry

B

Ben Zhong Tang

School of Science and Engineering, Guangdong Basic Research Center of Excellence for Aggregate Science, The Chinese University of Hong Kong (Shenzhen), Longgang, Shenzhen 518172, Guangdong, P. R. China

R

Ruquan Ye

Department of Chemistry and State Key Laboratory of Marine Environmental Health