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基于TiC/CoS复合阳极的具有优异倍率性能和循环稳定性的高度可逆锂离子电池。

Highly Reversible Lithium-Ion Battery with Excellent Rate Performance and Cycle Stability Based on a TiC/CoS Composite Anode.

作者信息

Tian Shuhao, Wang Di, Liu Zhe, Liu Guo, Zeng Qi, Sun Xiao, Yang Hongcen, Han Cong, Tao Kun, Peng Shanglong

机构信息

National & Locai Joint Engineering Laboratory for Optical Conversion Materials and Technology, School of Materials and Energy, Lanzhou University, Lanzhou 730000, P. R. China.

School of Physical Science and Technology, Lanzhou University, Lanzhou 730000, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44996-45004. doi: 10.1021/acsami.3c09605. Epub 2023 Sep 12.

Abstract

Transition metal sulfide (TMS) CoS is considered an ideal anode material for new-generation lithium-ion batteries (LIBs) because of its high specific capacity, high electrochemical activity, and low cost. However, CoS is prone to volume expansion and structural collapse when it participates in the internal conversion reaction of the battery, which limits its practical application. After analyzing the failure mechanism of CoS as the anode material of LIBs, the concept of nanoengineered materials is introduced here. CoS particles are nanosized and stabilized by constructing a composite structure on an alkali-treated two-dimensional TiC Mxene conductive network. Both experiments and theoretical calculations show that special Ti-O-Co bonds are formed at the interface of the TiC/CoS composite through oxygen-containing functional groups. Ti-O-Co bonding with adjustable electronic characteristics can effectively promote the utilization rate of anode materials, electronic conductivity, and ionic diffusivity and thus enhance the redox reaction kinetics of the device. When the TiC/CoS composite is used as the anode material for LIBs, it still provides a high specific capacity of 405.8 mAh g after 100 cycles at 0.1 A g. After running for 1000 cycles at a high current of 1 A g, the capacity retention is still close to 100%. Also, high cycle stability under the condition of highly active material loading (10.58 mg cm) and low electrolyte/active material ratio (10 μL mg) is achieved. This work provides a new idea for the development of commercial LIBs as anode materials.

摘要

过渡金属硫化物(TMS)硫化钴因其高比容量、高电化学活性和低成本,被认为是新一代锂离子电池(LIBs)的理想负极材料。然而,硫化钴在参与电池内部转化反应时容易发生体积膨胀和结构坍塌,这限制了其实际应用。在分析了硫化钴作为锂离子电池负极材料的失效机制后,本文引入了纳米工程材料的概念。通过在碱处理的二维TiC MXene导电网络上构建复合结构,使硫化钴颗粒纳米化并得到稳定。实验和理论计算均表明,通过含氧基官能团在TiC/CoS复合材料的界面处形成了特殊的Ti-O-Co键。具有可调节电子特性的Ti-O-Co键能有效提高负极材料的利用率、电子导电性和离子扩散率,从而增强器件的氧化还原反应动力学。当TiC/CoS复合材料用作锂离子电池的负极材料时,在0.1 A g下循环100次后仍具有405.8 mAh g的高比容量。在1 A g的高电流下运行1000次循环后,容量保持率仍接近100%。此外,在高活性材料负载量(10.58 mg cm)和低电解液/活性材料比(10 μL mg)的条件下也实现了高循环稳定性。这项工作为开发商业化锂离子电池负极材料提供了新思路。

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