Synergistic Catalysts for Lithium-Sulfur Batteries: Ni Single Atom and MoC Nanoclusters Composites

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-03-06 DOI:10.1002/anie.202502177
Chongchong Zhao, Yanxia Liu, Feng Huo, Zhenzhen Guo, Yurui Lu, Bowen Sun, Meng Li, Hui Xu, Min Zhang, Hailin Fan, Zixu Sun, Andreu Cabot, Yatao Zhang
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Abstract

The practical application of sulfur (S) cathodes in lithium-sulfur (Li-S) batteries is hindered by the shuttling of soluble lithium polysulfides (LiPSs) and sluggish sulfur redox kinetics. Addressing these challenges requires advanced catalytic host materials capable of trapping LiPSs and accelerating Li-S redox reactions. However, single-site catalysts struggle to effectively mediate the complex multi-step and multi-phase sulfur conversion processes. In this study, we present a novel dual-site catalyst, Ni-MoC-NC, featuring nickel single atoms anchored to nitrogen sites (Ni-N4) within a carbon nitride (NC) matrix and molybdenum carbide (MoC) nanoclusters. Experimental and theoretical analyses reveal that MoC sites efficiently catalyze the reduction of long-chain LiPSs (Li₂S₈ to Li₂S₄), while Ni-N4 sites drive the reduction of short-chain LiPSs (Li₂S₄ to Li₂S), resulting in a synergistic enhancement of the complete Li-S redox process. When incorporated as a coating on the cathode side of a commercial polypropylene (PP) separator, the Ni-MoC-NC catalyst enhances sulfur utilization, suppresses LiPSs shuttling, and facilitates a uniform Li+-ion distribution, effectively mitigating the uncontrolled growth of lithium dendrites. Thereby, Li-S batteries employing an S/Ni-MoC-NC cathode and a Ni-MoC-NC@PP separator demonstrate outstanding performance, including an initial capacity of 1624 mAh g⁻¹ at 0.2C and 1142 mAh g⁻¹ at 1C, retaining 590 mAh g⁻¹ after 800 cycles. At a sulfur loading of 8.3 mg cm⁻2 and an electrolyte/sulfur ratio of 6 µL mg⁻¹, the system achieves an initial areal capacity of 9.57 mAh cm⁻2 at 0.1C, showcasing significant promise for practical applications.

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锂硫电池的协同催化剂:Ni单原子和MoC纳米团簇复合材料
硫(S)阴极在锂硫(Li-S)电池中的实际应用受到可溶性锂多硫化物(LiPSs)的穿梭和硫氧化还原动力学缓慢的阻碍。解决这些挑战需要能够捕获LiPSs并加速Li-S氧化还原反应的先进催化宿主材料。然而,单位点催化剂难以有效地介导复杂的多步、多相硫转化过程。在这项研究中,我们提出了一种新的双位点催化剂,其特征是镍单原子锚定在氮化碳(NC)基体和碳化钼(MoC)纳米簇中的氮位点(Ni-N4)上。实验和理论分析表明,MoC位点对长链LiPSs的还原有较好的催化作用,而Ni-N4位点对短链LiPSs的还原有较好的催化作用。当将Ni-MoC-NC催化剂作为涂层涂在商用聚丙烯(PP)分离器的阴极侧时,可以提高硫的利用率,抑制lips的穿梭,并促进Li+离子的均匀分布。因此,锂- s电池表现出出色的性能,包括0.2C时1624毫安的初始容量和1C时1142毫安的初始容量。在8.3 mg cm - 2的硫负荷和6 μ L mg - 1的电解质/硫比下,该系统在0.1C时达到9.57 mAh cm - 2的初始面积容量,显示出实际应用的重大前景。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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