The Polymeric Sulfur Hosts From Ferrocene-Based Metal-Organic Framework@Ti3C2 Array Structure for Upgrading Energy Density and Longevity of Lithium-Sulfur Batteries
Bowen Chang, Tiankuo Xu, Dan Wang, Jiayu Huang, Xiaofei Xie, Xiaoju Li, Ruihu Wang
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引用次数: 0
Abstract
Polymeric sulfur is emerging as a cathode active material for lithium-sulfur (Li─S) batteries, which can effectively inhibit polysulfide shuttling through the formation of C─S covalent bonds. However, low conductivity and poor electrocatalytic activity of polymeric sulfur severely counteract the electrochemical performance, especially for high-sulfur-loading cathodes. Herein, it is presented one type of new polymeric sulfur host materials composed of ferrocene-based nickel metal-organic framework (NiFc) loaded on the surface of Ti3C2 nanosheets (Ti3C2@NiFc), which is prepared through inverse vulcanization reaction between NiFc and sulfur element. The sulfur copolymers significantly accelerate the redox kinetics and effectively inhibit polysulfide shuttling during cycling. The resultant electrode delivers a high gravimetric capacity of 1162 mAh g−1, the areal capacity of 8.37 mAh cm−2 and a volumetric capacity of 1146 mAh cm−3 at 0.2 C. The electrochemical performance can rival the reported state-of-the-art those in Li-S batteries. This work provides new protocols for the development of polymeric sulfur cathode materials to achieve high energy density and long life of Li-S batteries.
聚合物硫作为锂硫(Li─S)电池的正极活性材料正在兴起,它可以有效地抑制多硫化物通过形成C─S共价键而穿梭。然而,聚合物硫的低电导率和较差的电催化活性严重影响了其电化学性能,特别是对于高硫负荷量的阴极。本文提出了一种将二茂铁基镍金属有机骨架(NiFc)负载在Ti3C2纳米片表面(Ti3C2@NiFc)的新型聚合物硫载体材料,该材料是通过NiFc与硫元素的反硫化反应制备的。硫共聚物显著加快了氧化还原动力学,有效抑制了循环过程中多硫化物的穿梭。所得电极在0.2℃时具有1162 mAh g−1的高重量容量,8.37 mAh cm−2的面容量和1146 mAh cm−3的体积容量。电化学性能可与目前报道的锂电池相媲美。本工作为聚合物硫正极材料的开发提供了新的方案,以实现锂硫电池的高能量密度和长寿命。
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
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