加压物理活性炭:一种面向锂硫电池应用的高性能、经济型的正极载体材料OA
Pressurized physically activated carbon used as a high-performance,low cost cathode material in lithium-sulfur batteries
锂硫(Li―S)电池因其高能量密度及潜在成本优势,被认为是下一代储能体系的有力候选.传统的化学活性炭(CAC)因具有较高的比表面积、可实现较高的硫负载,常被用作Li―S电池正极载体材料.我们此前开发了一种加压物理活化方法,制备得到比表面积与CAC相当的活性炭(加压物理活化炭:PPAC).本研究进一步调控了PPAC的孔结构,并考察其作为Li―S电池正极材料的适用性.在不同倍率下的电化学测试表明,PPAC展现出显著提升的高倍率性能:在 1 C条件下,其放电比容量达到 900 mAh/g,而CAC仅为 600 mAh/g.孔结构分析显示,高活化温度制备的PPAC在作为人造炭材料基本结构单元的微域之间形成了独特的介孔通道.该微域间的介孔通道与微域内发育的微孔相连,构建了离子在外部与内部孔隙之间传输的有效路径.PPAC中同时充分发育的微孔与介孔分别保证了对多硫化锂的高吸附能力和较快的离子扩散速率.与传统的CAC相比,PPAC兼具高性能、低成本与孔结构可调等优势,因而在未来Li-S电池的工业化应用中具有广阔前景.
Lithium-sulfur(Li-S)batteries are prom-ising candidates for next-generation energy storage given their high energy density and potential low cost.Chemically activated carbon(CAC)is often used for their cathodes,because it has a high specific surface area for sulfur loading.We have developed a pressur-ized physical activation(PPA)method that produced an activated carbon(PPAC)with a high specific sur-face area comparable to that of CAC.The pore structure of PPAC could be changed and its use as a cathode material for Li-S batteries was investigated.Battery tests at different capacity rates(C-rates)showed that it had a much improved high-rate per-formance with a discharge capacity of 900 mAh/(g of sulfur)at 1 C,in contrast to only 600 mAh/(g of sulfur)for CAC.Pore structure analyses showed that PPAC prepared at a high activation temperature(1000 ℃)had unusual channel-like mesopores between the microdomains that are the basic structural units of artificial carbon materials.These are connected to micropores developed in each microdomain,and deliver ions from the surroundings to the internal pores and vice versa.The well-de-veloped micropores and mesopores of PPAC respectively ensured the high adsorption of lithium polysulfides and a high rate of ion diffusion.Compared to CAC,PPAC is a high-performance,low-cost cathode material that is promising for use in future Li-S batteries.
李明昊;王章骁;高红叶;波多聪;中林康治;尹圣昊;宫胁仁
九州大学,综合理工学府,福冈 春日,816-8580 日本九州大学,综合理工学府,福冈 春日,816-8580 日本九州大学,超显微解析研究中心,福冈 西区,819-0395 日本九州大学,综合理工学府,福冈 春日,816-8580 日本||九州大学,超显微解析研究中心,福冈 西区,819-0395 日本||九州大学,综合理工学研究院,福冈 春日,816-8580 日本九州大学,综合理工学府,福冈 春日,816-8580 日本||九州大学,先导物质研究所,福冈 春日,816-8580 日本九州大学,综合理工学府,福冈 春日,816-8580 日本||九州大学,先导物质研究所,福冈 春日,816-8580 日本九州大学,综合理工学府,福冈 春日,816-8580 日本||九州大学,先导物质研究所,福冈 春日,816-8580 日本
活性炭加压物理活化介孔通道锂硫电池微域
Activated carbonPressurized physical activationMesoporous channelLithium-sulfur batteriesMicrodo-main
《新型炭材料(中英文)》 2026 (1)
127-141,15
This work was supported by JST SPRING,Grant Number JPMJSP2136.The authors thank ASAHI YUKIZAI CORPORATION for providing spherical phenol resins.日本科学技术振兴机构(JST)SPRING(JPMJSP2136).
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