Anion intercalation enables efficient and stable carboxylate upgrading via aqueous non-Kolbe electrolysis

Next-generation techniques for sustainable carboxylate production generate carboxylate salts as the primary outcome. To circumvent the costly conversion of carboxylate salts to acids, we demonstrate the aqueous (non-)Kolbe electrolysis process as an alternative strategy to generate downstream value-added chemicals. Upon revealing the irreversible oxidation-induced charge transfer inhibition on the graphite anode, we propose an anion intercalation strategy to mitigate the stability problem induced by the ever-increasing overpotential. In acetate decarboxylation, we observe a high Faradaic efficiency of ~95% for non-Kolbe products (methanol and methyl acetate) at wide current densities ranging from 0.05 to 1 A cm<sup>-2</sup> and long-term stability at current densities of 0.15 and 0.6 A cm<sup>-2</sup> for 130 and 35 h, respectively. We also extended this strategy for the upgrading of long-chain carboxylates such as propionate, butyrate, and succinate. Our work provides valuable guidance for carboxylate upgrading and extendable strategy for overcoming passivation challenges in catalysis.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-04-19
DOI
https://doi.org/10.1038/s41467-025-58924-x
Citations
6
Primary Topic
Covalent Organic Framework Applications
Type
article
Field-Weighted Citation Impact
3.11

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Anion intercalation enables efficient and stable carboxylate upgrading via aqueous non-Kolbe electrolysis

Chuan Xia, Weiqing Xue, Tingting Zheng, Jie Zeng et al.
6 citations
Nature Communications
Covalent Organic Framework Applications
3.11
article

Anion intercalation enables efficient and stable carboxylate upgrading via aqueous non-Kolbe electrolysis

Chuan Xia, Weiqing Xue, Tingting Zheng, Jie Zeng, Qiu Jiang, Peitao Liu, Xu Li, Yongsheng Ji, Xinran Feng, Chunxiao Liu, Xinyan Zhang, Jun Luo, Laihao Luo, Donghao Zhao
article en
6 citations

Abstract

Next-generation techniques for sustainable carboxylate production generate carboxylate salts as the primary outcome. To circumvent the costly conversion of carboxylate salts to acids, we demonstrate the aqueous (non-)Kolbe electrolysis process as an alternative strategy to generate downstream value-added chemicals. Upon revealing the irreversible oxidation-induced charge transfer inhibition on the graphite anode, we propose an anion intercalation strategy to mitigate the stability problem induced by the ever-increasing overpotential. In acetate decarboxylation, we observe a high Faradaic efficiency of ~95% for non-Kolbe products (methanol and methyl acetate) at wide current densities ranging from 0.05 to 1 A cm<sup>-2</sup> and long-term stability at current densities of 0.15 and 0.6 A cm<sup>-2</sup> for 130 and 35 h, respectively. We also extended this strategy for the upgrading of long-chain carboxylates such as propionate, butyrate, and succinate. Our work provides valuable guidance for carboxylate upgrading and extendable strategy for overcoming passivation challenges in catalysis.

Nature CommunicationsVol. 16(1)
University of Science and Technology of China (CN), University of Electronic Science and Technology of China (CN), Hefei National Center for Physical Sciences at Nanoscale (CN), Anhui University of Technology (CN)
National Key Research and Development Program of China
Clean water and sanitation
Openalex Percentile: Top 8%
Covalent Organic Framework Applications
3.11
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.