材料科学
阴极
锂(药物)
兴奋剂
扩散
化学工程
石墨烯
纳米壳
扩散阻挡层
离子
电导率
纳米技术
物理化学
光电子学
纳米颗粒
物理
热力学
图层(电子)
化学
内分泌学
工程类
医学
量子力学
作者
Longwei Liang,Xuan Sun,Jinyang Zhang,Linrui Hou,Jinfeng Sun,Yang Liu,Shuguang Wang,Changzhou Yuan
标识
DOI:10.1002/aenm.201802847
摘要
Abstract Olivine‐type LiMnPO 4 (LMP) cathodes have gained enormous attraction for Li‐ion batteries (LIBs), thanks to their large theoretical capacity, high discharge platform, and thermal stability. However, it is still hugely challenging to achieve encouraging Li‐storage behaviors owing to their low electronic conductivity and limited lithium diffusion. Herein, the core double‐shell Ti‐doped LMP@NaTi 2 (PO 4 ) 3 @C/3D graphene (TLMP@NTP@C/3D‐G) architecture is designed and constructed via an in situ synthetic methodology. A continuous electronic conducting network is formed with the unfolded 3D‐G and conducting carbon nanoshell. The Nasicon‐type NTP nanoshell with exceptional ionic conductivity efficiently inhibits gradual enrichment in by‐products, and renders low surfacial/interfacial electron/ion‐diffusion resistance. Besides, a rapid Li + diffusion in the bulk structure is guaranteed with the reduction of Mn Li+ ˙ antisite defects originating from the synchronous Ti‐doping. Benefiting from synergetic contributions from these design rationales, the integrated TLMP@NTP@C/3D‐G cathode yields high initial discharge capacity of ≈164.8 mAh g −1 at 0.05 C, high‐rate reversible capacity of ≈116.2 mAh g −1 at 10 C, and long‐term capacity retention of ≈93.3% after 600 cycles at 2 C. More significantly, the electrode design developed here will exert significant impact upon constructing other advanced cathodes for high‐energy/power LIBs.
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