Defect-riched prussian blue analogues with superior adsorption-catalysis toward lithium polysulfides for high performance lithium-sulfur batteries

被引:0
|
作者
Qi, Wentao [1 ]
Zhou, Changhong [1 ]
Yang, Chao [1 ]
Ling, Rui [1 ]
机构
[1] Qufu Normal Univ, Sch Phys & Phys Engn, Qufu 273165, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium-sulfur batteries; Crystal defects; Active sites; lithium polysulfide; Prussian blue analogues; METAL-ORGANIC FRAMEWORK; CONVERSION;
D O I
10.1016/j.est.2024.114594
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Lithium-sulfur batteries (Li-S) garner significant interest within the energy storage industry, because of their exceptional theoretical energy density coupled with employment of environmental materials. Nevertheless, the broader implementation of Li-S batteries faces challenges, primarily due to the lithium polysulfide (LiPSs) shuttle effect and the sluggish conversion kinetics associated with LiPSs. In this work, we introduce a reduction- induced dissolution process to fabricate a mesoporous CoFePB rich in crystal defects via a facile solvothermal method. The experimental results indicate that the abundance of crystal defects originate from the phase transition from Co3[FeIII(CN)6]2 to Co2[FeII(CN)6]. The subsequent adsorption tests and electrochemical evaluations have shown that the defect-rich CoFePB possesses enhanced LiPSs absorption capacity and improved cycling performance in contrast to the pristine CoFePB, which is primarily ascribed to proliferation of active sites emerging as a result of the crystal defects. Consequently, the D-CoFePB-S cathode demonstrates remarkable rate performance with 583 mAh g- 1 at a substantial 5C current rate, superior long-term stability with capacity retention of 64.3 % over 2000 cycles at current rate of 2C and outstanding areal capacity of 4.9 mAh cm- 2 at 0.1C, even under a substantial sulfur loading of 5.0 mg cm- 2 .
引用
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页数:9
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