Paštika Jan, Güngen Deniz, Subramani Amutha, Mazánek Vlastimil, Serra Marco, Zeng Lunjie, Olsson Eva, Gusmão Rui, Sofer Zdeněk
Department of Inorganic Chemistry, Faculty of Chemical Technology, University of Chemistry and Technology Prague, Technická 5, Prague 6, Prague 166 28, Czech Republic.
Istituto Italiano di Tecnologia Via Morego 30, Genova 16163, Italy.
ACS Appl Mater Interfaces. 2025 Jun 18;17(24):35522-35532. doi: 10.1021/acsami.5c05482. Epub 2025 Jun 4.
High-entropy alloys have emerged as a class of materials, offering unique properties due to their irregular and randomized arrangement of multiple elements in an ordered lattice. This concept has been extended to two-dimensional (2D) van der Waals materials, including transition metal dichalcogenides (TMD), which exhibit promising applications in electrocatalysis. In this work, we have explored the synthesis of entropy mixture crystals (TMD) involving the chemical vapor transport of five individual elements, Mo and W as metal elements, S, Se, and Te as chalcogenide elements, resulting in a crystalline structure with a controlled composition MoW(SSeTe), with an estimated Δ of 0.96. When observed along the [001] zone axis, STEM HAADF images indicate the presence of the different crystal phases of the 2D TMDs (1T, 2H, and 3R). Our findings demonstrate the potential of the entropy TMD materials as catalysts for the hydrogen evolution reaction, offering an alternative to noble metal-based catalysts. To maximize the potential of TMD, we chose chemical exfoliation with the resulting material being subdivided into size groups, big and small, according to their lateral size. In an acidic medium, the lowest overpotential of 127 mV and a Tafel slope of 79 mV/dec were obtained for the exfoliated sample with a small lateral size (exf-TMD).
高熵合金已成为一类材料,由于其多种元素在有序晶格中不规则且随机排列,因而具有独特性能。这一概念已扩展到二维(2D)范德华材料,包括过渡金属二硫属化物(TMD),其在电催化方面展现出广阔应用前景。在本工作中,我们探索了熵混合晶体(TMD)的合成,涉及五种单独元素的化学气相传输,其中Mo和W为金属元素,S、Se和Te为硫属元素,最终得到一种成分可控的晶体结构MoW(SSeTe),估计其Δ为0.96。沿[001]晶带轴观察时,扫描透射电子显微镜高角度环形暗场(STEM HAADF)图像表明存在二维TMD的不同晶相(1T、2H和3R)。我们的研究结果证明了熵TMD材料作为析氢反应催化剂的潜力,为基于贵金属的催化剂提供了一种替代方案。为了最大化TMD的潜力,我们选择了化学剥离法,并根据横向尺寸将所得材料分为大小两组。在酸性介质中,横向尺寸较小的剥离样品(exf-TMD)获得了127 mV的最低过电位和79 mV/dec的塔菲尔斜率。