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通过可及电极设计实现二硫化钼粉末的可扩展电化学剥离

Toward Scalable Electrochemical Exfoliation of Molybdenum Disulfide Powder through an Accessible Electrode Design.

作者信息

Wilson Nicholas David, Ozhukil Valappil Manila, Martin Barbara Y, Siu Teri, Pennings Joel, Mackintosh Mira, Almadhoun Mahmoud N, Ouyang Jianying, Graddage Neil, Pope Michael A

机构信息

Department of Chemical Engineering, University of Waterloo, Waterloo, ON, N2L 3G1, Canada.

Security and Disruptive Technologies Research Center, National Research Council Canada, Ottawa, ON, K1A 0R6, Canada.

出版信息

Small Methods. 2025 Jan;9(1):e2400298. doi: 10.1002/smtd.202400298. Epub 2024 Jul 17.

Abstract

Cathodic electrochemical intercalation/exfoliation of transition metal dichalcogenides (TMDs) with bulky tetraalkylammonium-based cations is gaining popularity as it avoids the semiconducting (2H) to metallic (1T) phase transformation in TMDs like molybdenum disulfide (MoS) and, generally, produces sheets with a larger aspect ratio - important for achieving conformal sheet-to-sheet contact in optoelectronic devices. Large single crystals are typically used as the precursor, but these are expensive, often inaccessible, and result in limited quantities of material. In this paper, a 3D-printable electrochemical cell capable of intercalating gram-scale quantities of commercially available TMD powders is presented. By incorporating a reference electrode in the cell and physically restraining the powder with a spring-loaded mechanism, the system can probe the intercalation electrochemistry, for example, determining the onset of intercalation to be near -2.5 V versus the ferrocene redox couple. While the extent of intercalation depends on precursor quantity and reaction time, a high yield of exfoliated product can be obtained exhibiting average aspect ratios as high as 49 ± 44 similar to values obtained by crystal intercalation. The intercalation and exfoliation of a wide variety of pelletized commercial powders including molybdenum diselenide (MoSe), tungsten diselenide (WSe), tungsten disulfide (WS), and graphitic carbon nitride (gCN) are also demonstrated.

摘要

过渡金属二硫属化物(TMDs)与庞大的四烷基铵基阳离子的阴极电化学插层/剥离正变得越来越流行,因为它避免了二硫化钼(MoS)等TMDs中从半导体(2H)到金属(1T)的相变,并且通常会产生具有更大纵横比的薄片——这对于在光电器件中实现薄片与薄片之间的共形接触很重要。通常使用大单晶作为前驱体,但这些成本高昂,往往难以获得,并且产量有限。在本文中,展示了一种能够插入克级商业可用TMD粉末的3D可打印电化学电池。通过在电池中加入参比电极并用弹簧加载机制物理约束粉末,该系统可以探测插层电化学,例如确定相对于二茂铁氧化还原对,插层起始电压接近-2.5 V。虽然插层程度取决于前驱体数量和反应时间,但可以获得高产率的剥离产物,其平均纵横比高达49±44,与通过晶体插层获得的值相似。还展示了包括二硒化钼(MoSe)、二硒化钨(WSe)、二硫化钨(WS)和石墨相氮化碳(gCN)在内的各种造粒商业粉末的插层和剥离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4341/11740928/a1d4db6efbf5/SMTD-9-2400298-g001.jpg

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