多硫化物
石墨烯
化学工程
成核
材料科学
催化作用
溶解
电解质
吸附
法拉第效率
电催化剂
氧化物
纳米颗粒
纳米技术
无机化学
化学
电化学
电极
物理化学
有机化学
工程类
冶金
作者
Yuan Meng,Haodong Shi,Cong Dong,Shuanghao Zheng,Kai Wang,Shaoxu Wang,Zhong‐Shuai Wu
出处
期刊:2D materials
[IOP Publishing]
日期:2022-03-17
卷期号:9 (2): 025028-025028
被引量:4
标识
DOI:10.1088/2053-1583/ac5ec6
摘要
Abstract Some vital challenges are main obstacles for further development of lithium–sulfur (Li–S) batteries such as low capacity and poor cycle stability resulted from polysulfide shuttling behavior, the physical/chemical entrapment is regarded as an effective method to inhibit and catalyze polysulfides. Herein we design a cross-linked framework of reduced graphene oxide anchored with Cu 2− x Se nanoparticles (Cu 2− x Se@rGO) by building an electrolyte/Cu 2− x Se/graphene triple-phase interface to be a high-efficiency electrocatalyst for Li–S batteries. Importantly, this three-dimensional conductive network possesses a large specific surface area with high ion transport capability, meanwhile providing strong physical constraint for efficient adsorption of soluble polysulfides. Further, this triple-phase catalytic interface provides strong chemical adsorption and abundant Cu 2− x Se nanoparticle sulfiphilic active sites, effectively inhibiting the dissolution of polysulfides and guaranteeing the efficient polysulfide adsorption catalysis as well as rapidly uniform Li 2 S nucleation. Consequently, with the Cu 2− x Se@rGO separator, a lower capacity decay rate about 0.059% per cycle after 500 cycles at 2 C is obtained. What’s more, with a higher areal sulfur loading of 3.0 mg cm −2 , the capacity is still maintained at 805 mAh g −1 over 100 cycles. Therefore, this work will open new avenue to construct 2D transition metal selenide for superior performance Li–S batteries.
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