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过渡金属二硫化物纳米材料作为析氢反应电催化剂的通用胶体合成法

General Colloidal Synthesis of Transition-Metal Disulfide Nanomaterials as Electrocatalysts for Hydrogen Evolution Reaction.

作者信息

Meerbach Christian, Klemmed Benjamin, Spittel Daniel, Bauer Christoph, Park Young Jin, Hübner René, Jeong Hu Young, Erb Denise, Shin Hyeon Suk, Lesnyak Vladimir, Eychmüller Alexander

机构信息

Physical Chemistry, TU Dresden, Bergstr. 66b, 01062 Dresden, Germany.

Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 18;12(11):13148-13155. doi: 10.1021/acsami.9b21607. Epub 2020 Mar 9.

Abstract

The material-efficient monolayers of transition-metal dichalcogenides (TMDs) are a promising class of ultrathin nanomaterials with properties ranging from insulating through semiconducting to metallic, opening a wide variety of their potential applications from catalysis and energy storage to optoelectronics, spintronics, and valleytronics. In particular, TMDs have a great potential as emerging inexpensive alternatives to noble metal-based catalysts in electrochemical hydrogen evolution. Herein, we report a straightforward, low-cost, and general colloidal synthesis of various 2D transition-metal disulfide nanomaterials, such as MoS, WS, NiS, FeS, and VS, in the absence of organic ligands. This new preparation route provides many benefits including relatively mild reaction conditions, high reproducibility, high yields, easy upscaling, no post-thermal annealing/treatment steps to enhance the catalytic activity, and, finally, especially for molybdenum disulfide nanosheets, high activity in the hydrogen evolution reaction. To underline the universal application of the synthesis, we prepared mixed CoMoS nanosheets in one step to optimize the catalytic activity of pure undoped MoS, which resulted in an enhanced hydrogen evolution reaction performance characterized by onset potentials as low as 134 mV and small Tafel slopes of 55 mV/dec.

摘要

过渡金属二硫属化物(TMDs)的材料高效单分子层是一类很有前景的超薄纳米材料,其性质从绝缘到半导体再到金属,为从催化、储能到光电子学、自旋电子学和谷电子学等各种潜在应用开辟了广阔前景。特别是,TMDs作为电化学析氢中贵金属基催化剂的新兴廉价替代品具有巨大潜力。在此,我们报道了一种在无有机配体情况下直接、低成本且通用的胶体合成各种二维过渡金属二硫化物纳米材料(如MoS、WS、NiS、FeS和VS)的方法。这种新的制备路线具有许多优点,包括相对温和的反应条件、高重现性、高产率、易于放大、无需后热退火/处理步骤来提高催化活性,最后,特别是对于二硫化钼纳米片,在析氢反应中具有高活性。为强调该合成方法的广泛适用性,我们一步制备了混合CoMoS纳米片以优化纯未掺杂MoS的催化活性,其析氢反应性能得到增强,起始电位低至134 mV,塔菲尔斜率小至55 mV/dec。

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