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在实现高度稳定的钠金属阳极方面,具有可调厚度的超薄石墨烯薄膜起着至关重要的作用。

Critical Role of Ultrathin Graphene Films with Tunable Thickness in Enabling Highly Stable Sodium Metal Anodes.

机构信息

Thayer School of Engineering, Dartmouth College , 14 Engineering Drive, Hanover, New Hampshire 03755, United States.

出版信息

Nano Lett. 2017 Nov 8;17(11):6808-6815. doi: 10.1021/acs.nanolett.7b03071. Epub 2017 Oct 23.

DOI:10.1021/acs.nanolett.7b03071
PMID:29039955
Abstract

Sodium (Na) metal has shown great promise as an anode material for the next-generation energy storage systems because of its high theoretical capacity, low cost, and high earth abundance. However, the extremely high reactivity of Na metal with organic electrolyte leads to the formation of unstable solid electrolyte interphase (SEI) and growth of Na dendrites upon repeated electrochemical stripping/plating, causing poor cycling performance, and serious safety issues. Herein, we present highly stable and dendrite-free Na metal anodes over a wide current range and long-term cycling via directly applying free-standing graphene films with tunable thickness on Na metal surface. We systematically investigate the dependence of Na anode stability on the thickness of the graphene film at different current densities and capacities. Our findings reveal that only a few nanometer (∼2-3 nm) differences in the graphene thickness can have decisive influence on the stability and rate capability of Na anodes. To achieve the optimal performance, the thickness of the graphene film covered on Na surface needs to be meticulously selected based on the applied current density. We demonstrate that with a multilayer graphene film (∼5 nm in thickness) as a protective layer, stable Na cycling behavior was first achieved in carbonate electrolyte without any additives over 100 cycles at a current density as high as 2 mA/cm with a high capacity of 3 mAh/cm. We believe our work could be a viable route toward high-energy Na battery systems, and can provide valuable insights into the lithium batteries as well.

摘要

钠(Na)金属因其高理论容量、低成本和高地球丰度,作为下一代储能系统的阳极材料具有很大的前景。然而,Na 金属与有机电解质的极高反应性导致不稳定的固体电解质界面(SEI)的形成和 Na 枝晶的生长,从而导致循环性能差和严重的安全问题。在此,我们通过直接在 Na 金属表面施加具有可调厚度的独立式石墨烯薄膜,在宽电流范围和长期循环中实现了高度稳定且无枝晶的 Na 金属阳极。我们系统地研究了在不同电流密度和容量下,石墨烯薄膜厚度对 Na 阳极稳定性的依赖关系。我们的研究结果表明,石墨烯厚度仅相差几个纳米(约 2-3nm),就可以对 Na 阳极的稳定性和倍率性能产生决定性的影响。为了获得最佳性能,需要根据应用的电流密度仔细选择覆盖在 Na 表面的石墨烯薄膜的厚度。我们证明,通过使用多层石墨烯薄膜(约 5nm 厚)作为保护层,在没有任何添加剂的碳酸盐电解质中,在高达 2mA/cm 的电流密度下,以 3mAh/cm 的高容量,首次实现了稳定的 Na 循环行为,循环次数超过 100 次。我们相信,我们的工作可能是实现高能 Na 电池系统的可行途径,并且对锂离子电池也有重要的启示。

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