Dual-Carbon confinement strategy of antimony anode material enabling advanced potassium ion storage

阳极 石墨烯 材料科学 碳纤维 化学工程 电极 电化学 循环伏安法 复合数 纳米技术 化学 复合材料 冶金 物理化学 工程类
作者
Jiefeng Zheng,Yuanji Wu,Tong Yong,Yingjuan Sun,Hongyan Li
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:622: 738-747 被引量:16
标识
DOI:10.1016/j.jcis.2022.04.154
摘要

Antimony (Sb) has attracted considerable attention as an anode material for potassium ion batteries (PIBs) because of its high theoretical capacity. Nevertheless, owing to the large radius of K+, apparent volume expansion occurs during the reaction between Sb and K+, which will undermine the stability of the electrode. Accordingly, a dual-carbon confinement strategy is regarded as an effective method for handling this issue. Herein, Sb is firstly captured by mesoporous carbon sphere (MCS) to form a composite of Sb/MCS, and then reduced graphene oxide (rGO) is adopted as an outer layer to wrap the Sb/MCS to obtain the dual-carbon confinement material (Sb/MCS@rGO). Given the synergistic confinement effects of the MCS and rGO, the Sb/MCS@rGO electrode realizes an excellent rate capacity of 341.9 mAh g-1 at 1000 mA g-1 and prominent cycling stability with around 100% retention at 50 mA g-1 after 100 cycles. Besides, the discussion on galvanostatic charge-discharge test, cyclic voltammetry and ex-situ XRD illustrates the stepwise potassium storage mechanism of Sb. Benefiting from the dual-carbon confinement effects, the Sb/MCS@rGO electrode processes promising electrochemical reaction kinetics. Furthermore, the application of the Sb/MCS@rGO in full cells also demonstrates its superior rate capacity (212.3 mAh g-1 at 1000 mA g-1).
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