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高度分散的镍纳米晶体与源自单一来源的石墨化碳之间的协同作用作为高性能锂硫电池的一种策略。

Synergy between highly dispersed Ni nanocrystals and graphitized carbon derived from a single source as a strategy for high performance Lithium-Sulfur batteries.

作者信息

Soler-Piña Francisco Javier, Morales Julián, Caballero Álvaro

机构信息

Dpto. Química Inorgánica e Ingeniería Química, Instituto Químico para la Energía y el Medioambiente (IQUEMA), Universidad de Córdoba, Córdoba 14071, Spain.

Dpto. Química Inorgánica e Ingeniería Química, Instituto Químico para la Energía y el Medioambiente (IQUEMA), Universidad de Córdoba, Córdoba 14071, Spain.

出版信息

J Colloid Interface Sci. 2023 Jun 15;640:990-1004. doi: 10.1016/j.jcis.2023.03.035. Epub 2023 Mar 7.

DOI:10.1016/j.jcis.2023.03.035
PMID:36913837
Abstract

Due to their higher energy density, lower prices, and more environmentally friendly active components, Li-S batteries will soon compete with the current Li-ion batteries. However, issues persist that hinder this implementation, such as the poor conductivity of S and sluggish kinetics due to the polysulfide shuttle, among others. Herein, Ni nanocrystals encapsulated in a C matrix are obtained by a novel strategy based on the thermal decomposition of a Ni oleate-oleic acid complex at low-to-moderate temperatures: 500 and 700 °C. The two C/Ni composites were employed as hosts in Li-S batteries. Although the C matrix is amorphous at 500 °C, it is highly graphitized at 700 °C. At this moderate temperature, the simultaneous generation of Ni nanocrystals and the carbon matrix enhances the catalytic activity of Ni toward the graphitization process, which is negligible if starting from a mixture of a Ni salt and carbon source, even when calcined at temperatures as high as 1000 °C. The electrode made from the C/Ni composite obtained at 700 °C exhibits a high reversible capacity and an enhanced rate capability, much better not only than the C/Ni composite obtained at 500 °C but than others based on amorphous C calcined at very high temperatures, around 1000 °C. These properties are attributed to an increase in the electrical conductivity parallel to the ordering of the layers. We believe this work provides a new strategy to design C-based composites capable of combining the formation of nanocrystalline phases and the control of the C structure with superior electrochemical properties for Li-S batteries.

摘要

由于具有更高的能量密度、更低的价格以及更环保的活性成分,锂硫电池很快将与目前的锂离子电池展开竞争。然而,仍然存在一些问题阻碍其应用,比如硫的导电性差以及多硫化物穿梭导致的动力学迟缓等。在此,通过一种基于油酸镍 - 油酸络合物在中低温(500和700°C)下热分解的新策略,制备出了包裹在碳基质中的镍纳米晶体。这两种碳/镍复合材料被用作锂硫电池的主体材料。尽管在500°C时碳基质是非晶态的,但在700°C时它高度石墨化。在这个适中的温度下,镍纳米晶体和碳基质同时生成增强了镍对石墨化过程的催化活性,而如果从镍盐和碳源的混合物开始,即使在高达1000°C的温度下煅烧,这种催化活性也是可以忽略不计的。由700°C下获得的碳/镍复合材料制成的电极表现出高可逆容量和增强的倍率性能,不仅比500°C下获得的碳/镍复合材料好得多,而且比基于在约1000°C的非常高温度下煅烧的非晶碳的其他材料要好得多。这些性能归因于平行于层有序排列的电导率的增加。我们相信这项工作为设计基于碳的复合材料提供了一种新策略,这种复合材料能够将纳米晶相的形成与碳结构的控制相结合,并具有用于锂硫电池的优异电化学性能。

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