Size-dependent electrocatalytic hydrogen evolution activity of arrays of edge-like defects in MoS2 crystals patterned by focused ion beam

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-11-11 DOI:10.1039/d4ta05885b
Cláudia de Lourenço, Ana Beatriz Sorana de Araujo, Leonardo Hideki Hasimoto, Isaque A.A. Feitosa, Matheus Felipe Fagundes das Neves, Jefferson Bettini, Tarcísio Micheli Perfecto, Tulio C. R. Rocha, Thiago J.A. Mori, Edson R. Leite, Murilo Santhiago
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Abstract

Introducing surface defects on molybdenum disulfide (MoS2) crystals plays a crucial role in enhancing the electrocatalytic activity toward the hydrogen evolution reaction (HER). Despite the remarkable progress in this area, the precise control of the size, distance, and defective areas with minimal surface contamination remains unachieved. Conventional microfabrication methods often leave organic residues on the surface that impair electrocatalytic activity and hinder interface elucidation by advanced characterization tools. In this study, we pattern for the first-time arrays of pillars in nanometer-thick MoS2 flakes using a focused ion beam to enhance HER activity. We observe size-dependent stability of the edge-like defects under HER conditions with defective areas. The pillars undergo chemical and structural changes post-patterning due to an amorphization process, unambiguously confirmed by atomic force microscopy, Raman spectroscopy, and synchrotron X-ray photoelectron spectroscopy. Furthermore, the amorphization process is more pronounced in specific in-plane directions, as confirmed by transmission electron microscopy. The electrocatalytic activity of the pillars was measured using a recently reported fabrication method, allowing us to unequivocally correlate defects with HER activity. Microelectrodes with less pillars, i.e. less catalytic sites, demonstrate a lower overpotential of 349 mV at 10 mA cm-2 showcasing a groundbreaking advancement in their fabrication.
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聚焦离子束图案化的 MoS2 晶体边缘缺陷阵列的电催化氢气进化活性与尺寸有关
在二硫化钼(MoS2)晶体上引入表面缺陷对提高氢进化反应(HER)的电催化活性起着至关重要的作用。尽管在这一领域取得了令人瞩目的进展,但仍无法精确控制缺陷的大小、距离和缺陷区域,同时将表面污染降至最低。传统的微加工方法往往会在表面留下有机残留物,从而影响电催化活性,并阻碍先进表征工具对界面的阐释。在本研究中,我们首次使用聚焦离子束在纳米厚的 MoS2 片材上绘制了柱阵列,以增强 HER 活性。在 HER 条件下,我们观察到边缘样缺陷的稳定性与缺陷区域的尺寸有关。原子力显微镜、拉曼光谱和同步辐射 X 射线光电子能谱明确证实,由于非晶化过程,晶柱在图案化后发生了化学和结构变化。此外,透射电子显微镜也证实,在特定的平面方向上,非晶化过程更为明显。我们采用最近报道的一种制造方法测量了柱状物的电催化活性,从而明确了缺陷与 HER 活性之间的关系。在 10 mA cm-2 的条件下,柱子较少(即催化位点较少)的微电极显示出较低的过电位(349 mV),这表明其制造工艺取得了突破性进展。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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