周世晋, 韩文佳, 陈安祥, 张文浩, 焦丹丹, 李霞. 生物质基硬碳储钠负极材料研究进展[J]. 工程科学学报. DOI: 10.13374/j.issn2095-9389.2024.03.13.003
引用本文: 周世晋, 韩文佳, 陈安祥, 张文浩, 焦丹丹, 李霞. 生物质基硬碳储钠负极材料研究进展[J]. 工程科学学报. DOI: 10.13374/j.issn2095-9389.2024.03.13.003
Research progress on biomass-based hard carbon sodium storage anode materials[J]. Chinese Journal of Engineering. DOI: 10.13374/j.issn2095-9389.2024.03.13.003
Citation: Research progress on biomass-based hard carbon sodium storage anode materials[J]. Chinese Journal of Engineering. DOI: 10.13374/j.issn2095-9389.2024.03.13.003

生物质基硬碳储钠负极材料研究进展

Research progress on biomass-based hard carbon sodium storage anode materials

  • 摘要: 钠离子电池因其具有优异的低温性能、成本优势以及较高的安全性,有望逐渐成为锂离子电池的替代者,而限制钠离子电池发展的主要因素为负极材料,生物质基硬碳因其原料来源丰富、成本低廉、更易获得、碳产率高、环境友好且含有多种元素等优势而备受关注,其独特的微观结构在众多钠离子电池负极材料中展现出明显的优势和巨大的商业潜力。本文首先对钠离子在硬碳表面活性位点的吸附行为、进入石墨片层的过程顺序进行了分析,讨论了有争议的四种钠离子存储机制。不仅深入分析了钠离子在硬碳中的储存机理,还进一步讨论了不同生物质基前驱体硬碳的差异,并通过硬碳负极的微观结构提出钠离子电池负极的优化策略,对钠离子电池的发展具有一定的指导意义。

     

    Abstract: Sodium-ion batteries are expected to gradually become a replacement for lithium-ion batteries due to their excellent low-temperature performance, cost advantages and high safety, while the main factor limiting the development of sodium-ion batteries is the anode material. Because the size of sodium ions is larger than lithium ions, the graphite material applicable to the anode of lithium-ion batteries with long-range ordered structure can not be applied to sodium-ion batteries, while the hard carbon material has short graphite domains and chaotic arrangement, the internal short-range ordered structure of the carbon layer with local graphite area, the layer spacing is larger compared to the graphite, which is conducive to the storage of sodium ions, and the hard carbon is easier to obtain, high carbon yield, and environmental friendly. Biomass-based hard carbon has attracted much attention because of its abundant raw material sources, low cost, easier accessibility, high carbon yield, environmental friendliness, and multi-element content, etc. Its unique microstructure shows obvious advantages and great commercial potential among many anode materials for sodium-ion batteries. The storage mechanism of sodium ions in hard carbon is still controversial. In this paper, we firstly analyse the adsorption behaviour of sodium ions at the active sites on the hard carbon surface, the process sequence of entering the graphite flake layer, and review the four controversial sodium ion storage mechanisms. In this paper, not only the storage mechanism of sodium ions in hard carbon is deeply analysed, but also the differences of hard carbon with different biomass-based precursors are further discussed. The content of each component and microstructure varies among different precursors, and there are many differences between nut shells, woody and herbaceous stems, whose internal structural features and different component contents may play a key role in the hard carbon performance.This paper enumerates the structural and component differences between different biomass-based precursors, and then summarises the differences in the sodium storage performance of the hard carbons from different precursors. In order to enhance the sodium storage performance of biomass-based hard carbon, the optimisation strategy of sodium ion battery anode is proposed through the microstructure of hard carbon anode, such as the adjustment of carbon layer spacing, the adjustment of pore structure and its specific surface area, in addition to the elemental doping and the introduction of functional groups, which can also enhance the sodium storage performance of hard carbon, which is of some significance in guiding the development of sodium ion batteries.

     

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