Yifei Zhang, Duo Qi, Yitan Wang, Tianyu Wang, Yiran Tian, Bo Zhang, Na Wang
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引用次数: 0
Abstract
With the growing demand for secondary energy storage, potassium-ion batteries have garnered significant attention. However, the radius of potassium ions is too large, and the intercalation and detachment during charging and discharging will cause damage to the material structure. Therefore, the design and preparation of anode materials with high capacity and stability is the key to the development of potassium-ion batteries. Biomaterial has a significant place in energy storage for its utilization of renewable and cost-effective advantages. In this work, biomass branches are applied to serve as an inexpensive carbon precursor to fabricate porous carbon microstructure via hydrothermal treatment and a two-step activation method. The pore structure characteristics of the carbon were tuned by adjusting the activator ratio. This results in a porous structure with high conductivity, which is suitable for the rapid diffusion of potassium ions. The activated CK-1:4 successfully constructed a large number of mesoporous and microporous structures on the surface of the biochar by SEM and TEM tests, providing more active sites for the storage of potassium ions. When used as a PIB anode, CK-1:4 has a high reversible capacity of 108.4 mAh g−1 at 0.2 C and stable cycling performance (at a high current density of 0.2 C, it still exhibits an ultra-long cycling stability with a discharge capacity of 62.4 mAh g−1 after 1000 cycles). The in-depth electrochemical potassium storage mechanism is elaborated, which mainly relies on the capacitance-controlled contribution, further revealing the rapid reaction kinetics. In summary, the application of activated porous biochar materials to potassium-ion batteries can significantly improve the cycling performance of potassium-ion batteries. The results provide a new efficient and low-cost route for the development of anode materials for potassium-ion batteries.
随着二次储能需求的不断增长,钾离子电池备受关注。然而,钾离子的半径过大,充放电过程中的插层和脱离会对材料结构造成破坏。因此,设计和制备高容量、高稳定性的负极材料是钾离子电池发展的关键。生物材料具有可再生利用和成本效益高的优势,在储能领域占有重要地位。本研究以生物质枝条为廉价碳前驱体,通过水热处理和两步活化法制备多孔碳微结构。通过调整活化剂的比例来调整碳的孔隙结构特征。这使得多孔结构具有高导电性,适合钾离子的快速扩散。通过 SEM 和 TEM 测试,活化的 CK-1:4 成功地在生物炭表面构建了大量的介孔和微孔结构,为钾离子的储存提供了更多的活性位点。当用作 PIB 阳极时,CK-1:4 在 0.2 C 下具有 108.4 mAh g-1 的高可逆容量和稳定的循环性能(在 0.2 C 的高电流密度下,仍表现出超长循环稳定性,1000 次循环后的放电容量为 62.4 mAh g-1)。深入阐述了主要依靠电容控制贡献的电化学储钾机理,进一步揭示了快速反应动力学。总之,将活化多孔生物炭材料应用于钾离子电池可显著提高钾离子电池的循环性能。研究结果为钾离子电池负极材料的开发提供了一条高效、低成本的新途径。
期刊介绍:
The Journal of Materials Science: Materials in Electronics is an established refereed companion to the Journal of Materials Science. It publishes papers on materials and their applications in modern electronics, covering the ground between fundamental science, such as semiconductor physics, and work concerned specifically with applications. It explores the growth and preparation of new materials, as well as their processing, fabrication, bonding and encapsulation, together with the reliability, failure analysis, quality assurance and characterization related to the whole range of applications in electronics. The Journal presents papers in newly developing fields such as low dimensional structures and devices, optoelectronics including III-V compounds, glasses and linear/non-linear crystal materials and lasers, high Tc superconductors, conducting polymers, thick film materials and new contact technologies, as well as the established electronics device and circuit materials.