Carrasco Daniel F, García-Dalí Sergio, Villar-Rodil Silvia, Munuera José M, Raymundo-Piñero Encarnación, Paredes Juan I
Instituto de Ciencia y Tecnología del Carbono, INCAR-CSIC, Francisco Pintado Fe 26, Oviedo 33011, Spain.
CNRS, CEMHTI UPR3079, Univ. Orléans, 1D Avenue de la Recherche Scientifique, Orléans 45071, France.
ACS Appl Energy Mater. 2023 Jun 16;6(13):7180-7193. doi: 10.1021/acsaem.3c00893. eCollection 2023 Jul 10.
Layered transition-metal dichalcogenides (LTMDs) in two-dimensional (2D) form are attractive for electrochemical energy storage, but research efforts in this realm have so far largely focused on the best-known members of such a family of materials, mainly MoS, MoSe, and WS. To exploit the potential of further, currently less-studied 2D LTMDs, targeted methods for their production, preferably by cost-effective and sustainable means, as well as control over their nanomorphology, are highly desirable. Here, we report a quick and straightforward route for the preparation of 2D NbSe and other metallic 2D LTMDs that relies on delaminating their bulk parent solid under aqueous cathodic conditions. Unlike typical electrochemical exfoliation methods for 2D materials, which generally require an additional processing step (e.g., sonication) to complete delamination, the present electrolytic strategy yielded directly exfoliated nano-objects in a very short time (1-2 min) and with significant yields (∼16 wt %). Moreover, the dominant morphology of the exfoliated 2D NbSe products could be tuned between rolled-up nanosheets (nanorolls) and unfolded nanosheets, depending on the solvent where the nano-objects were dispersed (water or isopropanol). This rather unusual delamination behavior of NbSe was explored and concluded to occur via a redox mechanism that involves some degree of hydrolytic oxidation of the material triggered by the cathodic treatment. The delamination strategy could be extended to other metallic LTMDs, such as NbS and VSe. When tested toward electrochemical lithium storage, electrodes based on the exfoliated NbSe products delivered very high capacity values, up to 750-800 mA h g at 0.5 A g, where the positive effect of the nanoroll morphology, associated to increased accessibility of the lithium storage sites, was made apparent. Overall, these results are expected to expand the availability of fit-for-purpose 2D LTMDs by resorting to simple and expeditious production strategies of low environmental impact.
二维(2D)形式的层状过渡金属二硫属化物(LTMDs)在电化学储能方面具有吸引力,但迄今为止,该领域的研究主要集中在这类材料中最知名的成员,主要是MoS、MoSe和WS。为了进一步挖掘目前研究较少的二维LTMDs的潜力,非常需要有针对性的制备方法,最好是具有成本效益和可持续性的方法,以及对其纳米形态的控制。在此,我们报告了一种快速且直接的制备二维NbSe和其他金属二维LTMDs的方法,该方法依赖于在水相阴极条件下将其块状母体固体分层。与二维材料的典型电化学剥离方法不同,后者通常需要额外的处理步骤(如超声处理)来完成分层,本电解策略在非常短的时间(1 - 2分钟)内直接产生了剥离的纳米物体,且产率可观(约16 wt%)。此外,根据纳米物体分散的溶剂(水或异丙醇),剥离的二维NbSe产物的主要形态可以在卷曲纳米片(纳米卷)和展开纳米片之间调节。对NbSe这种相当不寻常的分层行为进行了探索,并得出结论,其发生是通过一种氧化还原机制,该机制涉及阴极处理引发的材料的某种程度的水解氧化。这种分层策略可以扩展到其他金属LTMDs,如NbS和VSe。当对电化学锂存储进行测试时,基于剥离的NbSe产物的电极在0.5 A g下提供了高达750 - 800 mA h g的非常高的容量值,其中纳米卷形态的积极作用与锂存储位点可及性的增加相关,这一点很明显。总体而言,这些结果有望通过采用简单且快速的、对环境影响小的生产策略来扩大适用的二维LTMDs的可用性。