Coke Kofi, Johnson Michael J, Robinson James B, Rettie Alexander J E, Miller Thomas S, Shearing Paul R
Electrochemical Innovation Lab, Department of Chemical Engineering, University College London, Torrington Place, London WC1E 7JE, U.K.
The Faraday Institution, Quad One, Becquerel Avenue, Harwell Campus, Didcot OX11 ORA, U.K.
ACS Appl Mater Interfaces. 2024 Apr 10;16(16):20329-40. doi: 10.1021/acsami.3c14612.
High-energy-density lithium sulfur (Li-S) batteries suffer heavily from the polysulfide shuttle effect, a result of the dissolution and transport of intermediate polysulfides from the cathode, into the electrolyte, and onto the anode, leading to rapid cell degradation. If this primary mechanism of cell failure is to be overcome, the distribution, dynamics, and degree of polysulfide transport must first be understood in depth. In this work, optical fluorescence microscope imaging of optically accessible Li-S cells is shown to enable real-time qualitative visualization of the spatial distribution of lithium polysulfides, both within the electrolyte and porous cathode. Quantitative determinations of spatial concentration are also possible at a low enough concentration. The distribution throughout cycling is monitored, including direct observation of polysulfide shuttling to the anode and consequent dendrite formation. This was enabled through the optimization of a selective fluorescent dye, verified to fluoresce proportionally with concentration of polysulfides within Li-S cells. This ability to directly and conveniently track the spatial distribution of soluble polysulfide intermediates in Li-S battery electrolytes, while the cell operates, has the potential to have a widespread impact across the field, for example, by enabling the influence of a variety of polysulfide mitigation strategies to be assessed and optimized, including in this work the LiNO additive.
高能量密度锂硫(Li-S)电池深受多硫化物穿梭效应之苦,这是由于中间多硫化物从阴极溶解并传输到电解质中,再到达阳极所致,从而导致电池迅速退化。如果要克服这种电池失效的主要机制,就必须首先深入了解多硫化物传输的分布、动力学和程度。在这项工作中,对光学可及的Li-S电池进行光学荧光显微镜成像,结果表明能够实时定性地可视化多硫化锂在电解质和多孔阴极中的空间分布。在足够低的浓度下也可以进行空间浓度的定量测定。监测整个循环过程中的分布情况,包括直接观察多硫化物向阳极的穿梭以及随之形成的枝晶。这是通过优化一种选择性荧光染料实现的,经证实该染料的荧光与Li-S电池中多硫化物的浓度成正比。在电池运行时直接且方便地跟踪Li-S电池电解质中可溶性多硫化物中间体的空间分布的这种能力,有可能在整个领域产生广泛影响,例如,通过评估和优化各种多硫化物缓解策略的影响,包括在这项工作中的LiNO添加剂。