Abstract

Paired electroreduction and electrooxidation of organics with water as a feedstock to produce value-added chemicals is meaningful. A comprehensive understanding of reaction mechanism is critical for the catalyst design and relative area development. Here, we have systematically studied the mechanism of the paired electroreduction and electrooxidation of organics on Fe-Mo-based phosphide heterojunctions. It is shown that active H* species for organic electroreduction originate from water. As for organic electrooxidation, among various oxygen species (OH*, OOH*, and O*), OH* free radicals derived from the first step of water dissociation are identified as active species. Furthermore, explicit reaction pathways and their paired advantages are proposed based on theoretical calculations. The paired electrolyzer powered by a solar cell shows a low voltage of 1.594 V at 100 mA cm−2, faradaic efficiency of ≥99%, and remarkable cycle stability. This work provides a guide for sustainable synthesis of various value-added chemicals via paired electrocatalysis.

Production of value-added chemicals by using renewable energy and cheap water attract great interest. Herein, the authors design a paired electrocatalytic system to produce 4-aminobenzyl alcohol at cathode and 2,5-furandicarboxylic acid at anode.

Details

Title
Unraveling the mechanism for paired electrocatalysis of organics with water as a feedstock
Author
Yang, Ganceng 1 ; Jiao, Yanqing 1 ; Yan, Haijing 1 ; Xie, Ying 1 ; Tian, Chungui 1 ; Wu, Aiping 1 ; Wang, Yu 1 ; Fu, Honggang 1 

 Key Laboratory of Functional Inorganic Material Chemistry Ministry of Education of the People’s Republic of China, Heilongjiang University, Harbin, China (GRID:grid.412067.6) (ISNI:0000 0004 1760 1291) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2673449509
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.