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双金属硫化物空心纳米立方体异质结构促进转化与合金化/脱合金反应的双重耦合以实现耐用的钾离子电池阳极

Bimetallic Sulfide Hollow Nanocubes Heterostructure Promotes Dual Coupling of Conversion and Alloying/Dealloying Reactions to Achieve Durable Potassium-Ion Battery Anode.

作者信息

Iqbal Sikandar, Wang Lu, Kong Zhen, Zhai Yanjun, Sun Xiuping, Wang Fengbo, Jing Zhongxin, He Xiyu, Mamoor Muhammad, Xu Liqiang

机构信息

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education and School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.

Shandong Provincial Key Laboratory/Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology, Liaocheng University, Liaocheng, Shandong, 252059, P. R. China.

出版信息

Small. 2024 Nov;20(45):e2404194. doi: 10.1002/smll.202404194. Epub 2024 Aug 13.

DOI:10.1002/smll.202404194
PMID:39136198
Abstract

Conversion and alloying-type transitional metal sulfides have attracted significant interests as anodes for Potassium-ion batteries (PIBs) and Sodium-ion batteries (SIBs) due to their high theoretical capacities and low cost. However, the poor conductivity, structural pulverization, and high-volume expansions greatly limit the performance. Herein, CoS/ZnS hollow nanocube-like heterostructure decorated on reduced graphene oxide (CoS/ZnS@rGO) composite is fabricated through convenient hydrothermal and post-heat vulcanization techniques. This unique composite can provide a more stable conductive network and shorten the diffusion length of ions, which exhibits a remarkable initial charge capacity of 638.5 mA h g at 0.1 A g for SIBs and 606 mA h g at 0.1 A g for PIBs, respectively; It is worth noting that the composite presents remarkable long stable cycle performance in PIBs, which initially delivered 274 mA h g and sustained the charge capacity up to 245 mA h g at high current density of 1 A g after 2000 cycles. A series of in situ/ex situ detections and first principle calculations further validate the high potassium ions adsorption ability of CoS/ZnS anode materials with high diffusion kinetics. This work will accelerate the fundamental construction of bimetallic sulfide hollow nanocubes heterostructure electrodes for energy storage applications.

摘要

由于具有高理论容量和低成本,转化型和合金化型过渡金属硫化物作为钾离子电池(PIBs)和钠离子电池(SIBs)的负极引起了广泛关注。然而,其导电性差、结构粉化和高体积膨胀极大地限制了其性能。在此,通过简便的水热和后热硫化技术制备了负载在还原氧化石墨烯上的CoS/ZnS中空纳米立方状异质结构复合材料(CoS/ZnS@rGO)。这种独特的复合材料能够提供更稳定的导电网络并缩短离子扩散长度,对于SIBs,在0.1 A g时其首次充电容量分别为638.5 mA h g,对于PIBs,在0.1 A g时为606 mA h g;值得注意的是,该复合材料在PIBs中表现出卓越的长循环稳定性,初始放电容量为274 mA h g,在1 A g的高电流密度下经过2000次循环后,充电容量仍保持在245 mA h g。一系列原位/非原位检测和第一性原理计算进一步验证了CoS/ZnS负极材料具有高钾离子吸附能力和高扩散动力学。这项工作将加速用于储能应用的双金属硫化物中空纳米立方异质结构电极的基础构建。

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