阳极
材料科学
基质(水族馆)
钠
蒸发
沉积(地质)
重量分析
电极
化学工程
化学
冶金
热力学
海洋学
物理
地质学
工程类
物理化学
古生物学
有机化学
生物
沉积物
作者
Hui Wang,Yan Wu,Shihao Liu,Yang Jiang,Dong Shen,Tianxing Kang,Zhongqiu Tong,Di Wu,Xinjian Li,Chun‐Sing Lee
标识
DOI:10.1002/smtd.202001050
摘要
While sodium metal anodes (SMAs) feature many performance advantages in sodium ion batteries (SIBs), severe safety concerns remain for using bulk sodium electrodes. Herein, a 3D Ag@C natrophilic substrate prepared by a facile thermal evaporation deposition method, which can be employed as a much safer "anode-free" SMA, is reported. Initially, there is no bulk sodium on the Ag@C substrate in the assembled SIBs. Upon charging, sodium will be uniformly deposited onto the Ag@C substrate and afterwards functions as a real SMA, thus inheriting the intrinsic merits of SMA and enhancing safety simultaneously. While cycling, the as-synthesized substrate demonstrates superior sodium plating/stripping cycling stability at 1, 2 and 3 mA cm-2 with a capacity of 2 mAh cm-2 . Theoretical simulations reveal that Na ions prefer to bind with Ag and form a Na-Ag network, thus clearly revealing uniform sodium deposition on the Ag@C substrate. More importantly, a full battery based on Ag@C and Prussian white with impressive Coulomb efficiency (CE), high rate capability (from 0.1 C to 5 C) and long-term cycling life is illustrated for the first time, thus making Ag@C feasible for the establishment of "anode-free" SIBs with reduced cost, high gravimetric/volumetric energy density and enhanced safety.
科研通智能强力驱动
Strongly Powered by AbleSci AI