Growing Intact Membrane by Tuning Carbon Down to Ultrasmall 0.37 nm Microporous Structure for Confining Dissolution of Polysulfides Toward High-Performance Sodium–Sulfur Batteries
IF 13 2区 材料科学Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Chao Wu, Juan Li, Lifei Liu, Heng Zhang, Zhuo Zou, Wei Sun, Fangyin Dai, Changming Li
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引用次数: 0
Abstract
Room temperature sodium–sulfur (Na–S) batteries are severely hampered by dissolution of polysulfides into electrolytes. Herein, a facile approach is used to tune a biomass-derived carbon down to an ultrasmall 0.37 nm microporous structure for the first time as a cathode in sodium–sulfur batteries. This produced an intact uniform Na2S membrane to greatly confine the dissolution of polysulfides while realizing a direct solid phase conversion for complete reduction of sulfur to Na2S, which delivers a sulfur loading of 1 mg cm−2 (50 wt.%), an excellent rate capacity (933 mAh g−1 @ 0.1 A g−1 and 410 mAh g−1 @ 2 A g−1), long cycle performance (0.036% per cycle decay at 1 A g−1 after 1500 cycles), and a high energy density for 373 Wh kg−1 (0.1 A g−1) based on whole electrode weight (active sulfur loading + carbon), ranking the best among all reported plain carbon cathode-based room temperature sodium–sulfur batteries in terms of the cycle life and rate capacity. It is proposed that the solid Na2S produced in the ultrasmall pores (0.37 nm) can be squeezed out to grow an intact membrane on the electrode surface covering the outlet of the pores and greatly depressing the dissolution effect of polysulfides for the long cycle life. This work provides a green chemistry to recycle wastes for sustainable energies and sheds light on design of a unique pore structure to effectively block the dissolution of polysulfides for high-performance sodium–sulfur batteries.
室温钠硫(Na-S)电池受到多硫化物溶解到电解质中的严重阻碍。本文采用一种简单的方法,首次将生物质衍生的碳调整为0.37 nm的超小微孔结构,作为钠硫电池的阴极。这就产生了一个完整均匀的Na2S膜,极大地限制了多硫化物的溶解,同时实现了直接固相转化,将硫完全还原为Na2S,其硫负载为1 mg cm - 2 (50 wt.%),具有优异的速率容量(933 mAh g - 1 @ 0.1 a g - 1和410 mAh g - 1 @ 2 a g - 1),长循环性能(经过1500次循环后,每循环在1 a g - 1下衰减0.036%)。基于全电极重量(活性硫负载+碳)的373 Wh kg−1 (0.1 a g−1)的高能量密度,在所有报道的普通碳阴极基室温钠硫电池中,在循环寿命和速率容量方面排名第一。结果表明,在0.37 nm的超细孔中产生的固体Na2S可以被挤出,在电极表面形成一层完整的膜,覆盖在孔的出口,大大抑制了多硫化物的溶解作用,从而延长了循环寿命。这项工作提供了一种绿色化学方法来回收废物以获得可持续能源,并为设计一种独特的孔隙结构提供了思路,该结构可以有效地阻止高性能钠硫电池中多硫化物的溶解。
期刊介绍:
Energy & Environmental Materials (EEM) is an international journal published by Zhengzhou University in collaboration with John Wiley & Sons, Inc. The journal aims to publish high quality research related to materials for energy harvesting, conversion, storage, and transport, as well as for creating a cleaner environment. EEM welcomes research work of significant general interest that has a high impact on society-relevant technological advances. The scope of the journal is intentionally broad, recognizing the complexity of issues and challenges related to energy and environmental materials. Therefore, interdisciplinary work across basic science and engineering disciplines is particularly encouraged. The areas covered by the journal include, but are not limited to, materials and composites for photovoltaics and photoelectrochemistry, bioprocessing, batteries, fuel cells, supercapacitors, clean air, and devices with multifunctionality. The readership of the journal includes chemical, physical, biological, materials, and environmental scientists and engineers from academia, industry, and policy-making.