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界面SbOC键和结构限制协同促进SbSe/NC纳米棒阳极用于钠存储的反应动力学和可逆性。

Interfacial SbOC bond and structural confinement synergistically boosting the reaction kinetics and reversibility of SbSe/NC nanorods anode for sodium storage.

作者信息

Shuai Honglei, Liu Renzhi, Li Wenxuan, Yang Xiaojian, Zhang Hao, Gao Yongping, Lu Hui, Huang Kejing

机构信息

School of Science and Technology, Xinyang College, Xinyang 464000, China.

School of Chemistry and Chemical Engineering, Guangxi Minzu University; Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission; Guangxi Key Laboratory of Chemistry and Engineering of Forest Products; Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products; Key Laboratory of Applied Analytical Chemistry (Guangxi Minzu University), Education Department of Guangxi Zhuang Autonomous Region, Nanning 530006, China.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt B):783-794. doi: 10.1016/j.jcis.2024.09.043. Epub 2024 Sep 8.

DOI:10.1016/j.jcis.2024.09.043
PMID:39270381
Abstract

Antimony selenide (SbSe) has been considered as a prospective material for sodium-ion batteries (SIBs) because of its large theoretical capacity. Whereas, grievous volume expansion caused by the conversion-alloying reaction leads to fast capacity decay and inferior cycle stability. Herein, the confined SbSe nanorods in nitrogen-doped carbon (SbSe/NC) with interfacial chemical bond is designed to further enhance sodium storage properties of SbSe. The robust enhancing effect of interfacial SbOC bonds can significantly promote electron transfer, Na ions diffusion kinetics and alloying reaction reversibility, combining the synergistic effect of the unique confinement structure of N-doped carbon shells can efficiently alleviate the volume change to ensure the structural integrity. Moreover, in-situ X-ray diffraction reveals intercalation/de-intercalation, conversion/reversed conversion reaction and alloying/de-alloying reaction mechanisms, and the kinetics analysis demonstrates the diffusion-controlled to contribute high capacity. As a result, SbSe/NC anode delivers a high reversible capacity of 612.6 mAh/g at 0.1 A/g with a retentive specific capacity of 471.4 mAh/g after 1000 cycles, and long-cycle durability of over 2000 cycle with the reversible capacities of 371.1 and 297.3 mAh/g at 1 and 2 A/g are achieved, respectively, and an good rate capability. This distinctive interfacial chemical bonds and confinement effect design shows potential applications in the improved conversion/alloying-type materials for SIBs.

摘要

硒化锑(SbSe)因其具有较大的理论容量,被认为是一种有前景的钠离子电池(SIBs)材料。然而,由转化-合金化反应引起的严重体积膨胀会导致快速的容量衰减和较差的循环稳定性。在此,设计了具有界面化学键的氮掺杂碳中受限的SbSe纳米棒(SbSe/NC),以进一步提高SbSe的储钠性能。界面SbOC键的强大增强作用可显著促进电子转移、Na离子扩散动力学和合金化反应的可逆性,结合氮掺杂碳壳独特的受限结构的协同效应,可有效缓解体积变化,确保结构完整性。此外,原位X射线衍射揭示了嵌入/脱嵌、转化/逆转化反应和合金化/脱合金化反应机制,动力学分析表明扩散控制有助于实现高容量。结果,SbSe/NC负极在0.1 A/g时具有612.6 mAh/g的高可逆容量,在1000次循环后比容量保持为471.4 mAh/g,在1 A/g和2 A/g时分别实现了超过2000次循环的长循环耐久性,可逆容量分别为371.1和297.3 mAh/g,并且具有良好的倍率性能。这种独特的界面化学键和受限效应设计在改进的SIBs转化/合金化型材料中显示出潜在的应用。

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