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钠硫电池中多硫化物的映射

Mapping Polysulfides in Sodium-Sulfur Batteries.

作者信息

Gray Esther Lilian, Lee Jung-In, Li Zhuangnan, Moloney James, Yang Ziwei Jeffrey, Chhowalla Manish

机构信息

Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB30FS, U.K.

出版信息

ACS Nano. 2025 Mar 11;19(9):8939-8947. doi: 10.1021/acsnano.4c16941. Epub 2025 Feb 28.

DOI:10.1021/acsnano.4c16941
PMID:40021486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11912571/
Abstract

Sodium-sulfur (Na-S) batteries provide lithium-free alternatives to lithium-sulfur (Li-S) batteries. Na-S chemistry has been less studied. Thus, the types of polysulfides (PS) and their evolution during charge-discharge of Na-S batteries are not as well understood as those in the Li-S system. We, therefore, study the formation of different PS in tetraethylene glycol dimethyl ether-based electrolyte during battery operation using Raman and ultraviolet-visible (UV-vis) spectroscopies. We start by making reference solutions with different ratios of sodium sulfide (NaS) to sulfur, ranging from pure NaS to NaS:7S, with the sulfur ratio increasing by one integer per solution. We then correlate the UV-vis and Raman peaks to PS species. Our galvanostatic charge-discharge (GCD) and cyclic voltammetry measurements show a total of ten features. Using UV-vis on aliquots and Raman spectra from PS solutions at GCD voltage plateaus, we map out sodium polysulfide (NaPS) species at key stages of the charge-discharge cycle. We identify NaS, NaS, and NaS as intermediates and NaS as the final product. We find that intermediate NaS forms from disproportionation of NaS and NaS. We also observe that intermediate PS can also dissociate into S radical species, which contributes to loss of active material. Our results provide detailed insights into Na-S chemistry that will be helpful for the development of high performance and stable batteries.

摘要

钠硫(Na-S)电池为锂硫(Li-S)电池提供了无锂的替代方案。对钠硫化学的研究较少。因此,钠硫电池中多硫化物(PS)的类型及其在充放电过程中的演变不如锂硫体系那样为人所熟知。因此,我们使用拉曼光谱和紫外可见(UV-vis)光谱研究了基于四甘醇二甲醚的电解质在电池运行过程中不同PS的形成。我们首先制备了不同硫化钠(NaS)与硫比例的参考溶液,范围从纯NaS到NaS:7S,每种溶液的硫比例增加一个整数。然后我们将UV-vis和拉曼峰与PS物种相关联。我们的恒电流充放电(GCD)和循环伏安法测量总共显示出十个特征。通过在GCD电压平台下对PS溶液的等分试样进行UV-vis测量和拉曼光谱分析,我们绘制了充放电循环关键阶段的多硫化钠(NaPS)物种图谱。我们确定NaS、NaS和NaS为中间体,NaS为最终产物。我们发现中间产物NaS由NaS和NaS的歧化反应形成。我们还观察到中间PS也可以分解为S自由基物种,这导致了活性材料的损失。我们的结果为钠硫化学提供了详细的见解,这将有助于高性能和稳定电池的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/d74f4f9842be/nn4c16941_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/fc0f2997e780/nn4c16941_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/bd4189cb1f7f/nn4c16941_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/7a0953ff68ee/nn4c16941_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/07ac4449175a/nn4c16941_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/ec0f7791f3a0/nn4c16941_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/117a5565c321/nn4c16941_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/d74f4f9842be/nn4c16941_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/fc0f2997e780/nn4c16941_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/bd4189cb1f7f/nn4c16941_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/7a0953ff68ee/nn4c16941_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/07ac4449175a/nn4c16941_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/ec0f7791f3a0/nn4c16941_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/117a5565c321/nn4c16941_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f866/11912571/d74f4f9842be/nn4c16941_0007.jpg

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本文引用的文献

1
Establishing reaction networks in the 16-electron sulfur reduction reaction.建立 16 电子硫还原反应中的反应网络。
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室温钠离子硫电池研究进展综述。
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Ultrastable Sodium-Sulfur Batteries without Polysulfides Formation Using Slit Ultramicropore Carbon Carrier.使用狭缝超微孔碳载体的无多硫化物形成的超稳定钠硫电池。
Adv Sci (Weinh). 2020 Apr 22;7(11):1903246. doi: 10.1002/advs.201903246. eCollection 2020 Jun.
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