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使用层状2H-MoTe作为负极的高性能锂离子电池。

High Performance Lithium-Ion Batteries Using Layered 2H-MoTe as Anode.

作者信息

Panda Manas Ranjan, Gangwar Rashmi, Muthuraj Divyamahalakshmi, Sau Supriya, Pandey Dhanshree, Banerjee Arup, Chakrabarti Aparna, Sagdeo Archna, Weyland Matthew, Majumder Mainak, Bao Qiaoliang, Mitra Sagar

机构信息

IITB Monash Research Academy, Bombay, Powai, Mumbai, 400076, India.

Department of Energy Science and Engineering, Electrochemical Energy Laboratory, Indian Institute of Technology Bombay, Powai, Mumbai, 400076, India.

出版信息

Small. 2020 Sep;16(38):e2002669. doi: 10.1002/smll.202002669. Epub 2020 Aug 16.

DOI:10.1002/smll.202002669
PMID:32803832
Abstract

The major challenges faced by candidate electrode materials in lithium-ion batteries (LIBs) include their low electronic and ionic conductivities. 2D van der Waals materials with good electronic conductivity and weak interlayer interaction have been intensively studied in the electrochemical processes involving ion migrations. In particular, molybdenum ditelluride (MoTe ) has emerged as a new material for energy storage applications. Though 2H-MoTe with hexagonal semiconducting phase is expected to facilitate more efficient ion insertion/deinsertion than the monoclinic semi-metallic phase, its application as an anode in LIB has been elusive. Here, 2H-MoTe , prepared by a solid-state synthesis route, has been employed as an efficient anode with remarkable Li storage capacity. The as-prepared 2H-MoTe electrodes exhibit an initial specific capacity of 432 mAh g and retain a high reversible specific capacity of 291 mAh g after 260 cycles at 1.0 A g . Further, a full-cell prototype is demonstrated by using 2H-MoTe anode with lithium cobalt oxide cathode, showing a high energy density of 454 Wh kg (based on the MoTe mass) and capacity retention of 80% over 100 cycles. Synchrotron-based in situ X-ray absorption near-edge structures have revealed the unique lithium reaction pathway and storage mechanism, which is supported by density functional theory based calculations.

摘要

锂离子电池(LIBs)中候选电极材料面临的主要挑战包括其低电子和离子电导率。具有良好电子导电性和弱层间相互作用的二维范德华材料在涉及离子迁移的电化学过程中得到了深入研究。特别是,二碲化钼(MoTe₂)已成为一种用于储能应用的新材料。尽管具有六方半导体相的2H-MoTe₂预计比单斜半金属相更有利于更高效的离子嵌入/脱嵌,但其作为LIBs阳极的应用一直难以实现。在此,通过固态合成路线制备的2H-MoTe₂已被用作具有显著锂存储容量的高效阳极。所制备的2H-MoTe₂电极初始比容量为432 mAh g⁻¹,在1.0 A g⁻¹下循环260次后仍保持291 mAh g⁻¹的高可逆比容量。此外,使用2H-MoTe₂阳极和钴酸锂阴极展示了一个全电池原型,其能量密度高达454 Wh kg⁻¹(基于MoTe₂质量),在100次循环中的容量保持率为80%。基于同步加速器的原位X射线吸收近边结构揭示了独特的锂反应途径和存储机制,这得到了基于密度泛函理论计算的支持。

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引用本文的文献

1
Band Alignments, Electronic Structure, and Core-Level Spectra of Bulk Molybdenum Dichalcogenides (MoS, MoSe, and MoTe).块状二硫化钼(MoS、MoSe和MoTe)的能带排列、电子结构及芯能级光谱
J Phys Chem C Nanomater Interfaces. 2022 Dec 15;126(49):21022-21033. doi: 10.1021/acs.jpcc.2c05100. Epub 2022 Dec 1.