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通过在非常规的基于磷含氧阴离子的电解质中进行等离子体电解来定制铜电极以增强一氧化碳电还原性能

Tailoring Cu Electrodes for Enhanced CO Electroreduction through Plasma Electrolysis in Non-Conventional Phosphorus-Oxoanion-Based Electrolytes.

作者信息

Elnagar Mohamed M, Menezes Pramod V, Parada Walter A, Mattausch Yannick, Kibler Ludwig A, Mayrhofer Karl J J, Jacob Timo

机构信息

Institute of Electrochemistry, Ulm University, 89069, Ulm, Germany.

Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (HI ERN), Egerlandstr. 3, 91058, Erlangen, Germany.

出版信息

ChemSusChem. 2023 Dec 7;16(23):e202300934. doi: 10.1002/cssc.202300934. Epub 2023 Sep 5.

Abstract

This study presents a green, ultra-fast, and facile technique for the fabrication of micro/nano-structured and porous Cu electrodes through in-liquid plasma electrolysis using phosphorous-oxoanion-based electrolytes. Besides the preferential surface faceting, the Cu electrodes exhibit unique surface structures, including octahedral nanocrystals besides nanoporous and microporous structures, depending on the employed electrolyte. The incorporation of P-atoms into the Cu surfaces is observed. The modified Cu electrodes display increased roughness, leading to higher current densities for CO electroreduction reaction. The selectivity of the modified Cu electrodes towards C products is highest for the Cu electrodes treated in Na HPO and Na PO electrolytes, whereas those treated in Na H PO produce the most H . The Cu electrode treated in Na PO produces ethylene (23 %) at -1.1 V vs. RHE, and a comparable amount of acetaldehyde (15 %) that is typically observed for Cu(110) single crystals. The enhanced selectivity is attributed to several factors, including the surface morphology, the incorporation of phosphorus into the Cu structure, and the formation of Cu(110) facets. Our results not only advance our understanding of the influence of the electrolyte's nature on the plasma electrolysis of Cu electrodes, but also underscores the potential of in-liquid plasma treatment for developing efficient Cu electrocatalysts for sustainable CO conversion.

摘要

本研究提出了一种绿色、超快速且简便的技术,用于通过使用基于磷氧阴离子的电解质进行液内等离子体电解来制备微/纳米结构和多孔的铜电极。除了优先的表面刻面外,根据所使用的电解质,铜电极还呈现出独特的表面结构,包括除了纳米多孔和微孔结构之外的八面体纳米晶体。观察到磷原子掺入到铜表面。改性后的铜电极显示出粗糙度增加,导致用于CO电还原反应的电流密度更高。在NaHPO和NaPO电解质中处理的铜电极对C产物的选择性最高,而在NaHPO中处理的铜电极产生的H最多。在NaPO中处理的铜电极在相对于可逆氢电极(RHE)为-1.1V时产生乙烯(23%),以及与Cu(110)单晶通常观察到的相当量的乙醛(15%)。选择性的提高归因于几个因素,包括表面形态、磷掺入铜结构以及Cu(110)面的形成。我们的结果不仅推进了我们对电解质性质对铜电极等离子体电解影响的理解,而且还强调了液内等离子体处理在开发用于可持续CO转化的高效铜电催化剂方面的潜力。

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