TiO2 nanotubular arrays decorated with ultrafine Ag nanoseeds enabling a stable and dendrite-free lithium metal anode

被引:2
|
作者
Li, Yulei [1 ]
Li, Shenhao [1 ]
Cui, Jiewu [1 ]
Yan, Jian [1 ]
Tan, Hark Hoe [2 ]
Liu, Jiaqin [1 ]
Wu, Yucheng [1 ]
机构
[1] Hefei Univ Technol, Key Lab Adv Funct Mat & Devices Anhui Prov, Engn Res Ctr Adv Composite Mat Design & Applicat, Inst Ind & Equipment Technol,Sch Mat Sci & Engn, Hefei 230009, Peoples R China
[2] Australian Natl Univ, Res Sch Phys & Engn, Dept Elect Mat Engn, Canberra, ACT 2601, Australia
来源
NANOSCALE ADVANCES | 2022年 / 4卷 / 21期
基金
中国国家自然科学基金;
关键词
A-stable - Ag nanocrystals - Cycling capacity - Li metal - Li-anodes - Lithium metal anode - Nanoseeds - Nanotubular - Ultra-fines - Ultrafine;
D O I
10.1039/d2na00526c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To exploit next-generation high-energy Li metal batteries, it is vitally important to settle the issue of dendrite growth accompanied by interfacial instability of the Li anode. Applying 3D current collectors as hosts for Li deposition emerges as a prospective strategy to achieve uniform Li nucleation and suppress Li dendrites. Herein, well-aligned and spaced TiO2 nanotube arrays grown on Ti foil and surface decorated with dispersed Ag nanocrystals (Ag@TNTAs/Ti) were constructed and employed as a 3D host for regulating Li stripping/plating behaviors and suppressing Li dendrites, and also relieving volume fluctuation during repetitive Li plating/stripping. Uniform TiO2 nanotubular structures with a large surface allow fast electron/ion transport and uniform local current density distribution, leading to homogeneous Li growth on the nanotube surface. Moreover, Ag nanocrystals and TiO2 nanotubes have good Li affinity, which facilitates Li+ capture and reduces the Li nucleation barrier, achieving uniform nucleation and growth of Li metal over the 3D Ag@TNTAs/Ti host. As a result, the as-fabricated Ag@TNTAs/Ti electrode exhibits dendrite-free plating morphology and long-term cycle stability with coulombic efficiency maintained over 98.5% even after 1000 cycles at a current density of 1 mA cm(-2) and cycling capacity of 1 mA h cm(-2). In symmetric cells, the Ag@TNTAs/Ti-Li electrode shows a much lower hysteresis of 40 mV over an ultralong cycle period of 2600 h at a current density of 1 mA cm(-2) and cycling capacity of 1 mA h cm(-2). Moreover, the full cell with the Ag@TNTAs/Ti-Li anode and LiFePO4 cathode achieves a high capacity of 155.2 mA h g(-1) at 0.5C and retains 77.9% capacity with an average CE of approximate to 99.7% over 200 cycles.
引用
收藏
页码:4639 / 4647
页数:9
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