硫化物
电解质
阳极
材料科学
化学工程
无机化学
多硫化物
硫黄
阴极
氮化物
分离器(采油)
金属
石墨氮化碳
化学
图层(电子)
电极
冶金
纳米技术
有机化学
物理
物理化学
光催化
催化作用
工程类
热力学
作者
Yao Zhao,Huichao Lü,Xirui Kong,Jun Yang,Yanna NuLi,Jiulin Wang
标识
DOI:10.1016/j.cej.2024.150887
摘要
Sulfide solid-state electrolytes (SSEs) are expected to fundamentally avoid the polysulfides shuttle and Li dendrites growth in the traditional liquid electrolyte lithium-sulfur (Li-S) batteries owing to its ultrahigh ionic conductivity, the high mechanical strength and favorable interfacial compatibility with sulfide-based cathodes. However, the sulfide SSEs are thermodynamically unstable to Li metal, and the parasitic reactions between the Li anode and sulfide SSEs results in intolerable interface deterioration. Herein, a graphitic carbon nitride (GCN, g-C3N4)-dominated artificial interlayer was introduced to enhance the interfacial stability between Li metal and sulfide SSEs. The introduction of electrochemically inert GCN is revealed to effectively alleviate the formation of heterogenous resistance layers for long-term. Furthermore, the abundant nitrogen species within GCN layer homogenize the distribution of Li ions flux, which effectively smooths Li deposition and suppresses dendrites growth. Herein, the symmetric cells with the Li-GCN show a stable plating/stripping cycling for over 1100 h at 0.2 mA cm−2 and a capacity of 0.2 mAh cm−2. The all-solid-state Li-SPAN battery with g-C3N4 interphase exhibits a highly reversible capacity of 579 mAh g−1 and a capacity retention of 88 % at 0.2C after 150 cycles, as well as achieves an excellent rate performance.
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