多硫化物
阳极
锂(药物)
锂硫电池
石墨烯
材料科学
氧化物
电镀(地质)
无机化学
化学工程
法拉第效率
阴极
电化学
电解质
金属
纳米技术
化学
冶金
电极
物理化学
内分泌学
工程类
地质学
医学
地球物理学
作者
Wantang Li,Min Han,Huan Li,Zijin Chen,Tongxin Shang,Zhitan Wu,Chen Zhang,Jia Li,Wei Lv,Ying Tao,Quan‐Hong Yang
标识
DOI:10.1002/batt.202000062
摘要
Abstract The shuttle effect of lithium polysulfides (LiPSs) from sulfur cathode to lithium (Li) anode is one of the main obstacles for lithium‐sulfur (Li−S) batteries. The severe corrosion of Li metal anode by the dissolved LiPSs bottlenecks the efficient operation of Li−S batteries, however, the anode part has not been received much attention compared to those extensive efforts related to the cathode designs. Herein, we show that the interface between Ti 3 C 2 T x (T=−OH, −F)‐based MXene and reduced graphene oxide (rGO) is able to guide uniform Li nucleation, promoting highly reversible and dendrite‐free Li plating/stripping. Such the Li anode demonstrates excellent cycling stability for more than 1000 hours even under ultra‐high rate (10 mA cm −2 ) and high areal capacity (3 mAh cm −2 ). More importantly, the well‐designed 2D layered structure by coupling the Ti 3 C 2 T x with a graphene scaffold, is highly efficient to block the shuttled polysulfides and inhibit the corrosion of the lithium metal anode. As a result, the Li−S full battery exhibits a stable cycling stability with a high Coulombic efficiency of 99.8 % over 300 cycles. This work suggests the design strategy of Li metal anode especially targeting at the sulfur cathode, and we hope it can provide valuable inspirations for the future design of Li metal anodes for more practical Li−S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI