生物碳介导的 MoS2 纳米胶体层间扩展和导电网络可增强钾离子存储能力

Shuo Zhang, Zonggui Yin, Lili Wang, Mengyao Shu, Xin Liang, Sheng Liang, Lei Hu, Chonghai Deng, Kunhong Hu, Xiaobo Zhu
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摘要

钾离子电池(PIB)是一种前景广阔的储能电池技术。然而,由于缺乏可快速、可重复容纳大量 K+ 离子的电极材料,钾离子电池的发展仍然受到阻碍。在此,我们利用生物质甘蔗渣设计了一种复合阳极材料,该材料在碳纳米网(MoS2/C@CNs)中含有层间扩展的 MoS2(大 55.6%)纳米软糖,生物质甘蔗渣中的双重碳源可分别转化为层间碳和骨架碳。与简单的 MoS2/C 复合材料和纯 MoS2 相比,这种独特的结构有利于整个电极的电子/离子传输,并具有出色的结构稳定性,从而大大提高了电化学性能。此外,研究人员还探讨了电解质盐(六氟磷酸钾和双氟磺酰亚胺钾)和电解质浓度对 PIB 的界面性能的影响。结果表明,低浓度双(氟磺酰)亚胺钾电解质有助于产生优化的有机-无机固态电解质界面薄膜,在 2 A g-1 的条件下循环 1,000 次后,容量保持率可达 90%。
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Interlayer expansion and conductive networking of MoS2 nanoroses mediated by bio-derived carbon for enhanced potassium-ion storage
Potassium-ion batteries (PIBs) represent a promising battery technology for energy storage applications. Nevertheless, the progress of PIBs is still hindered by the lack of electrode materials that allow rapid and repeatable accommodation of the large K+ ions. Herein, a composite anode material containing interlayered-expanded MoS2 (55.6% larger) nanoroses in carbon nanonets (MoS2/C@CNs) is designed with the assistance of biomass bagasse, of which the dual carbon sources convert into interlayer and skeleton carbon, respectively. The unique structure facilitates electron/ion transport in the entire electrode and offers excellent structural stability, leading to much improved electrochemical performance compared to simple MoS2/C composite and pure MoS2. Furthermore, the role of electrolyte salts (potassium hexafluorophosphate and potassium bis(fluorosulfonyl)imide) and the electrolyte concentration on the interfacial properties in PIBs have been explored. The results indicate that the low-concentration potassium bis(fluorosulfonyl)imide electrolyte helps to produce optimized organic-inorganic solid electrolyte interface films, contributing to a capacity retention of 90% after 1,000 cycles at 2 A g-1.
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