阳极
材料科学
电化学
锂(药物)
石墨烯
电子转移
拉曼光谱
离子
化学工程
电极
相(物质)
纳米技术
化学
物理化学
医学
物理
有机化学
工程类
光学
内分泌学
作者
Yang Yang,Jingxin Huang,Zhenming Cao,Zeheng Lv,Dong-zhen Wu,Zhipeng Wen,Weiwei Meng,Jing Zeng,Cheng Chao Li,Jinbao Zhao
出处
期刊:Advanced Science
[Wiley]
日期:2021-12-28
卷期号:9 (6): e2104530-e2104530
被引量:70
标识
DOI:10.1002/advs.202104530
摘要
Implementing fast-charging lithium-ion batteries (LIBs) is severely hindered by the issues of Li plating and poor rate capability for conventional graphite anode. Wadsley-Roth phase TiNb2 O7 is regarded as a promising anode candidate to satisfy the requirements of fast-charging LIBs. However, the unsatisfactory electrochemical kinetics resulting from sluggish ion and electron transfer still limit its wide applications. Herein, an effective strategy is proposed to synchronously improve the ion and electron transfer of TiNb2 O7 by incorporation of oxygen vacancy and N-doped graphene matrix (TNO- x @N-G), which is designed by combination of solution-combustion and electrostatic self-assembly approach. Theoretical calculations demonstrate that Li+ intercalation gives rise to the semi-metallic characteristics of lithiated phases (Liy TNO- x ), leading to the self-accelerated electron transport. Moreover, in situ X-ray diffraction and Raman measurements reveal the highly reversible structural evolution of the TNO- x @N-G during cycling. Consequently, the TNO- x @N-G delivers a higher reversible capacity of 199.0 mAh g-1 and a higher capacity retention of 86.5% than those of pristine TNO (155.8 mAh g-1 , 59.4%) at 10 C after 2000 cycles. Importantly, various electrochemical devices including lithium-ion full battery and hybrid lithium-ion capacitor by using the TNO- x @N-G anode exhibit excellent rate capability and cycling stability, verifying its potential in practical applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI