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通过长链全氟碳化合物的等离子体沉积制备具有电荷渗透性的疏水涂层。

Hydrophobic Coatings with Charge Permeability via Plasma Deposition of Long-Chain Perfluorocarbons.

作者信息

Delcheva Iliana, Weinfurter Anna, Hui Ka Wai, Gheorghiu Alexandru, Tran Thi Thuy Dung, Vasilev Krasimir, Mougel Victor, Harmer Sarah L, MacGregor Melanie N

机构信息

Institute for Nanoscale Science and Technology, Flinders University, Bedford Park, South Australia 5042, Australia.

Department of Chemistry and Applied Biosciences, Laboratory of Inorganic Chemistry ETH Zürich, Vladimir Prelog Weg. 1-5, CH-8093 Zürich, Switzerland.

出版信息

ACS Appl Energy Mater. 2024 Apr 29;7(13):5326-5337. doi: 10.1021/acsaem.3c03177. eCollection 2024 Jul 8.

Abstract

Hydrophobization of nanotextured catalyst materials is a promising route to enhance the yield of N and CO conversion into green fuels. However, these applications require a hydrophobic coating to not only promote air trapping but also allow charge transfer at the electrode-electrolyte interface. In this work, nano thin films with thicknesses as low as 7 nm were deposited from the plasma phase of perfluorohexene, perfluorodecene, and perfluorooctane (PFO) precursors using a mild vacuum and gentle powers. Atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS) characterization reveal that the resulting films are conformal and hydrophobic thanks to a good retention of CF and CF moieties. The PFO films exhibited the highest water contact angle and achieved superhydrophobic states when deposited on top of re-entrant nano features, an indication of successful air trapping. Electrochemical studies further demonstrated that the plasma-deposited PFO films allow charge transfer but could only sustain repeated cyclic voltammetry cycles without losing their hydrophobicity when deposited under optimal conditions. This result indicates that plasma deposition could become a viable route for the hydrophobization of electrocatalysts required to enhance the yield of poorly soluble gas reduction reactions.

摘要

对具有纳米纹理的催化剂材料进行疏水化处理是提高氮和一氧化碳转化为绿色燃料产率的一条有前景的途径。然而,这些应用要求疏水涂层不仅能促进空气捕获,还能在电极 - 电解质界面实现电荷转移。在这项工作中,使用适度的真空和温和的功率,从全氟己烯、全氟癸烯和全氟辛烷(PFO)前驱体的等离子体相中沉积出厚度低至7纳米的纳米薄膜。原子力显微镜(AFM)和X射线光电子能谱(XPS)表征表明,由于CF和CF基团的良好保留,所得薄膜具有保形性且疏水。PFO薄膜表现出最高的水接触角,当沉积在凹角纳米特征之上时达到超疏水状态,这表明成功捕获了空气。电化学研究进一步表明,等离子体沉积的PFO薄膜允许电荷转移,但只有在最佳条件下沉积时,才能承受重复的循环伏安法循环而不失去其疏水性。这一结果表明,等离子体沉积可能成为一种可行的途径,用于对提高难溶性气体还原反应产率所需的电催化剂进行疏水化处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a9c/11235096/f73e390cc67b/ae3c03177_0001.jpg

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