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用于将CO电还原为甲酸盐的三相界面工程化分级多孔电极

Triple-Phase Interface Engineered Hierarchical Porous Electrode for CO Electroreduction to Formate.

作者信息

Shi Tong, Liu Dong, Liu Ning, Zhang Ying, Feng Hao, Li Qiang

机构信息

State Key Laboratory of Multiphase Flow in Power Engineering, School of Energy and Power Engineering, Xi'an Jiaotong University, Xi'an, 710049, China.

MIIT Key Laboratory of Thermal Control of Electronic Equipment, School of Energy and Power Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.

出版信息

Adv Sci (Weinh). 2022 Oct;9(30):e2204472. doi: 10.1002/advs.202204472. Epub 2022 Sep 1.

Abstract

The aqueous electrochemical CO reduction to valuable products is seen as one of the most promising candidates to achieve carbon neutrality yet still suffers from poor selectivity and lower current density. Highly efficient CO reduction significantly relies on well-constructed electrode to realize efficient and stable triple-phase contact of CO , electrolyte, and active sites. Herein, a triple-phase interface engineering approach featuring the combination of hierarchical porous morphology design and surface modification is presented. A hierarchical porous electrode is constructed by depositing bismuth nanosheet array on copper foam followed by trimethoxy (1H,1H,2H,2H-heptadecafluorodecyl) silane modification on the nanosheet surface. This electrode not only achieves highly selective and efficient CO reduction performance with formate selectivity above 90% over wide potentials and a partial current density over -90 mA cm in H-cell but also maintains a superior stability during the long-term operation. It is demonstrated that this remarkable performance is attributed to the construction of efficient and stable triple-phase interface. Theoretical calculations also show that the modified surface optimizes the activation path by lowering thermodynamic barriers of the key intermediates *OCHO for the formation of formate during electrochemical CO reduction.

摘要

将水电化学CO还原为有价值的产物被视为实现碳中和最有前景的途径之一,但仍存在选择性差和电流密度较低的问题。高效的CO还原很大程度上依赖于精心构建的电极,以实现CO、电解质和活性位点的高效稳定三相接触。在此,提出了一种三相界面工程方法,其特点是将分级多孔形态设计与表面改性相结合。通过在泡沫铜上沉积铋纳米片阵列,然后在纳米片表面进行三甲氧基(1H,1H,2H,2H-十七氟癸基)硅烷改性,构建了一种分级多孔电极。该电极不仅在宽电位范围内实现了高选择性和高效的CO还原性能,在H型电池中甲酸根选择性高于90%,部分电流密度超过-90 mA cm,而且在长期运行过程中保持了优异的稳定性。结果表明,这种卓越的性能归因于高效稳定的三相界面的构建。理论计算还表明,改性表面通过降低电化学CO还原过程中形成甲酸根的关键中间体*OCHO的热力学势垒,优化了活化路径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88da/9596843/1376c6c80c2b/ADVS-9-2204472-g008.jpg

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