Xiaoke Luo, Di Wang, Shiyi Liu, Hailong Yan, Jinbing Cheng, Yang Lu, Deyang Zhang, Huan Pang
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Li-S batteries incorporating CoSe QDs/Sn<sub>3</sub>O<sub>4</sub> porous carbon nanofibers (PCNFs) demonstrate a high discharge capacity of 1596.9 mAh g<sup>-1</sup> at 0.1 C, along with remarkable cycling stability, achieving 1500 cycles at 2 C with a minimal capacity decay of 0.024 % per cycle. Even under a high sulfur loading conditions of 8.61 mg cm<sup>-2</sup> and a low electrolyte to sulfur ratio of approximately 4.6 μL mg<sup>-1</sup>, the CoSe QDs/Sn<sub>3</sub>O<sub>4</sub> PCNFs cathode delivers an initial discharge-specific capacity of 732.0 mAh g<sup>-1</sup> at 0.2 C. Through this method, we accomplished the size control and uniform distribution of CoSe QDs, and this method can be extended to the synthesis of other metal oxide and metal sulfide QDs, offering a novel idea for the application of QDs in polysulfide catalysis.</p>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"682 ","pages":"884-893"},"PeriodicalIF":9.4000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CoSe QDs/Sn<sub>3</sub>O<sub>4</sub> PCNFs with high catalytic conversion kinetics towards high-efficiency Li-S batteries.\",\"authors\":\"Xiaoke Luo, Di Wang, Shiyi Liu, Hailong Yan, Jinbing Cheng, Yang Lu, Deyang Zhang, Huan Pang\",\"doi\":\"10.1016/j.jcis.2024.12.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The redox reactions occurring at positive electrode of the lithium-sulfur (Li-S) batteries involve several key electrocatalytic processes that significantly impact the overall performance of the electrochemical energy storage system. 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引用次数: 0
摘要
锂硫电池正极发生的氧化还原反应涉及几个关键的电催化过程,这些过程对电化学储能系统的整体性能有重要影响。本研究提出了一种由CoSe量子点(QDs)与Sn3O4纳米片集成而成的非均相催化复合材料,该材料提高了阴极内整体离子电导率和活性位点的可及性。这种受控的迁移有效地捕获了阴极内的多硫化物,减少了它们在电解质中的溶解,减轻了穿梭效应。采用CoSe QDs/Sn3O4多孔碳纳米纤维(PCNFs)的Li-S电池在0.1 C下具有1596.9 mAh g-1的高放电容量,以及出色的循环稳定性,在2 C下可实现1500次循环,每次循环的最小容量衰减为0.024%。即使在高硫加载条件下的8.61毫克cm-2电解液和低硫比约为4.6μL mg-1,量子点聊天/ Sn3O4 PCNFs阴极提供一个初始discharge-specific容量732.0 mAh g - 1在0.2级c。通过这种方法,我们完成了量子点尺寸控制和均匀分布的谈心,和这种方法可以扩展到其他金属氧化物的合成量子点和金属硫化物,提供一个新奇的想法在聚硫催化量子点的应用。
CoSe QDs/Sn3O4 PCNFs with high catalytic conversion kinetics towards high-efficiency Li-S batteries.
The redox reactions occurring at positive electrode of the lithium-sulfur (Li-S) batteries involve several key electrocatalytic processes that significantly impact the overall performance of the electrochemical energy storage system. This study presents a heterogeneous catalytic composite material composed of CoSe quantum dots (QDs) integrated with Sn3O4 nanosheets, which enhances the overall ionic conductivity and accessibility of active sites within the cathode. This controlled migration effectively traps polysulfides within the cathode, reducing their dissolution into the electrolyte and mitigating the shuttle effect. Li-S batteries incorporating CoSe QDs/Sn3O4 porous carbon nanofibers (PCNFs) demonstrate a high discharge capacity of 1596.9 mAh g-1 at 0.1 C, along with remarkable cycling stability, achieving 1500 cycles at 2 C with a minimal capacity decay of 0.024 % per cycle. Even under a high sulfur loading conditions of 8.61 mg cm-2 and a low electrolyte to sulfur ratio of approximately 4.6 μL mg-1, the CoSe QDs/Sn3O4 PCNFs cathode delivers an initial discharge-specific capacity of 732.0 mAh g-1 at 0.2 C. Through this method, we accomplished the size control and uniform distribution of CoSe QDs, and this method can be extended to the synthesis of other metal oxide and metal sulfide QDs, offering a novel idea for the application of QDs in polysulfide catalysis.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies