Tuning the Closed Pore Structure of Hard Carbons with the Highest Na Storage Capacity

作者：Qingshi Meng, Yaxiang Lu, Feixiang Ding, Qiangqiang Zhang, Liquan Chen, Yong‐Sheng Hu · 发表于：ACS Energy Letters · 年份：2019 · DOI：10.1021/acsenergylett.9b01900 · 被引用次数：513 · 研究领域：Advancements in Battery Materials、Advanced Battery Materials and Technologies、Supercapacitor Materials and Fabrication

High-capacity anode materials are one of the bottlenecks to further improve the energy density of Na-ion batteries (NIBs). Except for introducing more defects to increase the sloping capacity, tuning the closed porous structure to boost the plateau capacity is another direction. Here by adopting phenol-formaldehyde resin (PF) as the carbon precursor and ethanol (EtOH) as the pore-forming agent, through precise chemical regulation of their relative content during a solvothermal process before further carbonization, carbon anodes with appropriate microstructure are achieved. It is found that the function of EtOH rests on generating steam vapor to create a pore cavity among cross-linked matrixes. The obtained optimal anodes exhibit a high Na storage capacity of ca. 410 mAh/g. When pairing with an O3-NaNi 1/3 Fe 1/3 Mn 1/3 O 2 cathode, the full cell delivers a high initial Coulombic efficiency of 83% and energy density of ca. 300 Wh/kg. The proposed chemical regulation approach via a pore-forming strategy is simple and practical to enable high-energy-density NIBs.