{"title":"Promoting Intermediate Stabilization and Coupling for Dimethyl Carbonate Electrosynthesis","authors":"Yuying Mi, Yuanyuan Xue, Yaqin Yan, Shuya Hao, Cejun Hu, Lijuan Zhang, Gengfeng Zheng","doi":"10.1002/smll.202501780","DOIUrl":null,"url":null,"abstract":"The electrocatalytic coupling of methanol and CO to produce dimethyl carbonate (DMC) is an attractive strategy for converting C<sub>1</sub> resources into value-added products, while the controlled adsorption and coupling of two key intermediates, <sup>*</sup>CO and <sup>*</sup>OCH<sub>3</sub>, have not been demonstrated yet. Herein, a heterointerface engineering strategy is developed to modulate intermediate adsorption and facilitate the C─O bond formation. By constructing a Pd and PdO heterostructure catalyst with abundant interfaces (designated as Pd/PdO-r), the Pd<sup>0</sup> sites serve to stabilize <sup>*</sup>CO and the electrophilic Pd<sup>2+</sup> sites can promote the <sup>*</sup>OCH<sub>3</sub> adsorption, thereby optimizing their spatial proximity and reactivity. In addition, the heterointerfaces allow to lower the coupling reaction barrier, enabling an efficient electrocatalytic pathway for the DMC synthesis. Consequently, the Pd/PdO-r heterostructure catalyst exhibited a high Faradaic efficiency of 86% with a DMC yield rate of 252 µmol h<sup>−1</sup> mg<sub>cat</sub><sup>−1</sup> in flow cells. The work suggests an effective approach to design heterointerfaces for enhanced intermediate adsorption and coupling, thus promoting the formation of valuable multicarbon products from C<sub>1</sub> resources.","PeriodicalId":228,"journal":{"name":"Small","volume":"114 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202501780","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The electrocatalytic coupling of methanol and CO to produce dimethyl carbonate (DMC) is an attractive strategy for converting C1 resources into value-added products, while the controlled adsorption and coupling of two key intermediates, *CO and *OCH3, have not been demonstrated yet. Herein, a heterointerface engineering strategy is developed to modulate intermediate adsorption and facilitate the C─O bond formation. By constructing a Pd and PdO heterostructure catalyst with abundant interfaces (designated as Pd/PdO-r), the Pd0 sites serve to stabilize *CO and the electrophilic Pd2+ sites can promote the *OCH3 adsorption, thereby optimizing their spatial proximity and reactivity. In addition, the heterointerfaces allow to lower the coupling reaction barrier, enabling an efficient electrocatalytic pathway for the DMC synthesis. Consequently, the Pd/PdO-r heterostructure catalyst exhibited a high Faradaic efficiency of 86% with a DMC yield rate of 252 µmol h−1 mgcat−1 in flow cells. The work suggests an effective approach to design heterointerfaces for enhanced intermediate adsorption and coupling, thus promoting the formation of valuable multicarbon products from C1 resources.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.