法拉第效率
阳极
材料科学
枝晶(数学)
金属
锌
成核
水溶液
电镀(地质)
电解质
化学工程
锂(药物)
无机化学
电极
冶金
化学
工程类
内分泌学
物理化学
有机化学
地质学
医学
数学
地球物理学
几何学
作者
Yuan Tian,Yongling An,Chuanliang Wei,Baojuan Xi,Shenglin Xiong,Jinkui Feng,Yitai Qian
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-10-04
卷期号:13 (10): 11676-11685
被引量:452
标识
DOI:10.1021/acsnano.9b05599
摘要
Dendrite growth of metal anodes is one of the key hindrances for both secondary aqueous metal batteries and nonaqueous metal batteries. In this work, a freestanding Ti3C2Tx MXene@Zn paper is designed as both zinc metal anode and lithium metal anode host to address the issue. The binder-free Ti3C2Tx MXene@Zn paper exhibits merits of good mechanical flexibility, high electronic conductivity, hydrophilicity, and lithiophilicity. The crystal growth mechanism of Zn metal on common Zn foil and Ti3C2Tx MXene@Zn composite is also studied. It is found that the Ti3C2Tx MXene@Zn paper can effectively suppress the dendrite growth of Zn, enabling reversible and fast Zn plating/stripping kinetics in an aqueous electrolyte. Moreover, the Ti3C2Tx MXene@Zn paper can be used as a 3D host for a lithium metal anode. In this host, Zn is utilized as a nucleation agent to suppress the Li dendrite growth. The freestanding Ti3C2Tx MXene@Zn@Li anode exhibits superior reversibility with high Coulombic efficiency (97.69% over 600 cycles at 1.0 mA cm–2) and low polarization compared with the Cu@Li anode. These findings may be useful for the design of dendrite-free metal-based energy storage systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI