Yuanqing He
;
Chongyang Ma
;
Shiheng Mo
;
Chung-Li Dong
;
Wei Chen
;
Shuo Chen
;
Huan Pang
;
Renzhi Ma
;
Shuangyin Wang
;
Yuqin Zou
説明:
(abstract)The electrochemical oxidation of 5-hydroxymethylfurfural (HMFOR) in alkaline electrolyte is a promising strategy for producing high-value chemicals from biomass derivatives. However, the disproportionation of aldehyde groups under strong alkaline conditions and the polymerization of HMF to form humic substances can impact the purity of 2,5-furandicarboxylic acid (FDCA) products. The use of neutral electrolytes offers an alternative environment for electrolysis, but the lack of OH− ions in the electrolyte often leads to low current density and low yields of FDCA. In this study, a sandwich-structured catalyst, consisting of Ru clusters confined between unilamellar MnO2 nanosheets (S-Ru/MnO2), was used in conjunction with an electrochemical pulse method to realize the electrochemical conversion of 5-hydroxymethylfurfural into FDCA in neutral electrolytes. Pulse electrolysis and the strong electron transfer between Ru clusters and MnO2 nanosheets help maintain Ru in a low oxidation state, ensuring high activity. The increased *OH generation led to a groundbreaking current density of 47 mA/cm2 at 1.55 V vs. reversible hydrogen electrode (RHE) and an outstanding yield rate of 98.7 % for FDCA in a neutral electrolyte. This work provides a strategy that combines electrocatalyst design with an electrolysis technique to achieve remarkable performance in neutral HMFOR.
権利情報:
キーワード: Electrocatalysts, Nanostructure, Electrochemical pulse
刊行年月日: 2024-09-12
出版者: Elsevier BV
掲載誌:
研究助成金:
原稿種別: 著者最終稿 (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.5335
公開URL: https://doi.org/10.1016/j.scib.2024.09.013
関連資料:
その他の識別子:
連絡先:
更新時刻: 2025-09-12 08:30:33 +0900
MDRでの公開時刻: 2025-09-12 08:18:13 +0900
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