Constructing hollow flower-like molybdenum disulfide nanospheres/carbon nanospheres as anode with enhanced diffusion kinetics for lithium storage

IF 23.2 2区 材料科学 Q1 MATERIALS SCIENCE, COMPOSITES Advanced Composites and Hybrid Materials Pub Date : 2024-10-23 DOI:10.1007/s42114-024-01029-8
Liyuan Liu, Wei Du, Qi Zhang, Huiyu Jiang, Yuping Zhang, Xiaoyang Yang, Xiubo Xie, Xueqin Sun, Chuanxin Hou
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Abstract

Molybdenum disulfide (MoS2) has been considered a potential candidate anode electrode for next-generation high-performance lithium-ion batteries (LIBs) in terms of its high theoretical capacity. Nevertheless, the unsatisfactory electrochemical behavior, including unstable cycling performance and poor rate capability, caused by low electronic conductivity, frail layered structure, and huge volumetric during cycling, hinders its practical application. Synthesizing MoS2-based composites with rationally designed structure and catalytic activity to boost the reaction kinetics of conversion reaction is important but still a challenge. In this work, hollow flower-like molybdenum disulfide nanospheres/carbon (MoS2/C) nanospheres were prepared via a facile solvothermal synthesis and heat treatment process. As expected, benefiting from the uniquely prepared hollow flower-like structure and the introduction of conductive carbon, the intrinsic drawbacks are effectively alleviated, resulting in super electrochemical performance of a high reversible capacity of 425.8 mAh g−1 at 20.0 A g−1, and a high capacity of 538.2 mAh g−1 with a high coulomb efficiency of over 99.9% after 1300 cycles at 1.0 A g−1. Furthermore, the quantitative kinetic analysis results prove that pseudo-capacitance dominates total capacity behavior (76.7% at 0.5 mV−1). Besides, the galvanostatic intermittent titration technique (GITT) was applied to identify the fast diffusion coefficient of the electrodes. This work offers an effective strategy for the subsequent preparation of transition metal sulfides for energy storage electrodes.

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构建空心花状二硫化钼纳米球/碳纳米球作为负极,增强锂存储的扩散动力学
二硫化钼(MoS2)具有很高的理论容量,一直被认为是下一代高性能锂离子电池(LIB)的潜在候选负极电极。然而,由于电子电导率低、层状结构脆弱、循环过程中体积巨大等原因,MoS2 的电化学性能并不理想,包括循环性能不稳定和速率能力差,这阻碍了它的实际应用。合成具有合理设计结构和催化活性的 MoS2 基复合材料以提高转化反应的反应动力学性能非常重要,但仍是一项挑战。本研究通过简便的溶热合成和热处理工艺制备了中空花状二硫化钼纳米球/碳(MoS2/C)纳米球。正如预期的那样,得益于独特的空心花状结构和导电碳的引入,其内在缺陷得到了有效缓解,从而实现了超强的电化学性能:在 20.0 A g-1 电流条件下,可逆容量高达 425.8 mAh g-1;在 1.0 A g-1 电流条件下,循环 1300 次后,容量高达 538.2 mAh g-1,库仑效率超过 99.9%。此外,定量动力学分析结果证明,伪电容在总容量行为中占主导地位(0.5 mV-1 时为 76.7%)。此外,还采用了电静电间歇滴定技术(GITT)来确定电极的快速扩散系数。这项研究为后续制备过渡金属硫化物储能电极提供了有效策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
26.00
自引率
21.40%
发文量
185
期刊介绍: Advanced Composites and Hybrid Materials is a leading international journal that promotes interdisciplinary collaboration among materials scientists, engineers, chemists, biologists, and physicists working on composites, including nanocomposites. Our aim is to facilitate rapid scientific communication in this field. The journal publishes high-quality research on various aspects of composite materials, including materials design, surface and interface science/engineering, manufacturing, structure control, property design, device fabrication, and other applications. We also welcome simulation and modeling studies that are relevant to composites. Additionally, papers focusing on the relationship between fillers and the matrix are of particular interest. Our scope includes polymer, metal, and ceramic matrices, with a special emphasis on reviews and meta-analyses related to materials selection. We cover a wide range of topics, including transport properties, strategies for controlling interfaces and composition distribution, bottom-up assembly of nanocomposites, highly porous and high-density composites, electronic structure design, materials synergisms, and thermoelectric materials. Advanced Composites and Hybrid Materials follows a rigorous single-blind peer-review process to ensure the quality and integrity of the published work.
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