锂(药物)
石墨氮化碳
碳纤维
极性(国际关系)
硫黄
氮化物
极性反转
材料科学
化学
纳米技术
工程类
电气工程
复合材料
有机化学
冶金
复合数
医学
催化作用
生物化学
图层(电子)
光催化
电压
细胞
内分泌学
作者
Martin M. F. Choi,Jinhyeon Jo,KwangSup Eom
标识
DOI:10.1021/acsaem.5c00754
摘要
Lithium–sulfur (Li–S) batteries are one of the most promising next-generation energy-storage systems due to their high energy density (2600 Wh kg–1). Nevertheless, the shuttle effect caused by the dissolution of lithium polysulfide (LiPS) interrupts the commercial application of Li–S batteries. Graphitic carbon nitride (GCN), with an enriched density of pyridinic-N sites for LiPS adsorption, has been explored as an effective adsorption material to inhibit the migration of polysulfides. However, the inferior conductivity of GCN imposes limitations on sulfur utilization in Li–S batteries. Herein, the boron-doped, nitrogen-defect GCN (BCN4–x) is designed as a slurry additive to synergistically enhance the adsorption strength of LiPS and the conductivity of GCN. Boron doping in GCN enhances positive polarization, improving the conductivity of GCN. Additionally, B-doping induces nitrogen defects and cyano groups, increasing the polarity of the GCN. Based on UV–Vis absorbance, BCN4–x exhibits a stronger affinity for LiPS compared to GCN. Moreover, compared to pristine GCN, BCN4–x achieved 20% higher capacity retention (71.33% after 100 cycles at 0.5 C) and 1.7 times greater rate performance (803.01 mAh g–1 at 1.0 C) in Li–S batteries due to a synergistic effect.
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