材料科学
阳极
碳化
微观结构
阴极
化学工程
碳纤维
阻燃剂
兴奋剂
形态学(生物学)
容量损失
纳米-
离子
纳米颗粒
纳米技术
扫描电子显微镜
复合材料
有机化学
化学
电极
物理化学
工程类
复合数
生物
遗传学
光电子学
作者
Tong Wang,Lingling Liu,Yanwei Wei,Yihan Gao,Shun Wang,Deqi Jia,Wei Zhang,Jingquan Sha
出处
期刊:Small
[Wiley]
日期:2023-12-10
卷期号:20 (20)
标识
DOI:10.1002/smll.202309809
摘要
Abstract The microstructure of hard carbons (HCs) including interlayer distance and lateral ab direction and pore size distribution plays a key role in regulating the sodium ions storage performance. Herein, by employing the gelatinous agar as a model precursor, series P‐doping HCs (P‐HC‐ x , x = 1, 2, 3, 4) are facilely prepared in batches via controllably regulating its crosslinking state by phytic acid (PA) at a low carbonization temperature of 750 °C, in which PA plays three roles (acid, flame retardant, and P‐doping precursor) in promoting the final structure of P‐HC‐x. Among those, the puparium like P‐HC‐2 with expanded carbon interlayer distance of 3.91 Å and shortened lateral ab direction of 9.4 nm delivers a high reversible capacity of 394 mAh g −1 at 0.1 A g −1 with high increased slope capacity of 363 mAh g −1 as well as an ultrafast charge‐discharge feature and a superlong cycle life. Pairing with the Na 3 V 2 (PO 4 ) 3 cathode, the fabricated sodium‐ion full cells exhibit the 132 mAh g −1 reversible capacity at 0.1 A g −1 , and 86% capacity retention after 100 cycles. This work successfully develops slope‐dominated high‐performance carbon anode, which will provide new insights for the microstructure regulation and design of other precursor‐derivedHCs.
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