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用于超长寿命“摇椅式”水系锌离子电池的分级结构二硫化钼双层纳米管的分子工程策略

Molecular Engineering Strategy to Construct Hierarchical MoS Double-Layer Nanotubes for Ultralong Lifespan "Rocking-Chair" Aqueous Zinc-Ion Batteries.

作者信息

Niu Feier, Bai Zhongchao, Chen Junming, Gu Qinfen, Wang Xuchun, Wei Jumeng, Mao Yueyuan, Dou Shi Xue, Wang Nana

机构信息

College of Chemistry and Materials Engineering, Anhui Science and Technology University, Bengbu 233000, P. R. China.

Anhui Province Quartz Sand Purification and Photovoltaic Glass Engineering Research Center, Bengbu 233000, P. R. China.

出版信息

ACS Nano. 2024 Feb 27;18(8):6487-6499. doi: 10.1021/acsnano.3c12034. Epub 2024 Feb 13.

DOI:10.1021/acsnano.3c12034
PMID:38349904
Abstract

Rechargeable aqueous zinc ion batteries (AZIBs) have gained considerable attention owing to their low cost and high safety, but dendrite growth, low plating/stripping efficiency, surface passivation, and self-erosion of the Zn metal anode are hindering their application. Herein, a one-step molecular engineering strategy for the simultaneous construction of hierarchical MoS double-layer nanotubes (MoS-DLTs) with expanded layer-spacing, oxygen doping, structural defects, and an abundant 1T-phase is proposed, which are designed as an intercalation-type anode for "rocking-chair" AZIBs, avoiding the Zn anode issues and therefore displaying a long cycling life. Benefiting from the structural optimization and molecular engineering, the Zn diffusion efficiency and interface reaction kinetics of MoS-DLTs are enhanced. When coupled with a homemade ZnMnO cathode, the assembled MoS-DLTs//ZnMnO full battery exhibited impressive cycling stability with a capacity retention of 86.6% over 10 000 cycles under 1 A g, outperforming most of the reported "rocking-chair" AZIBs. The Zn/H cointercalation mechanism of MoS-DLTs is investigated by synchrotron powder X-ray diffraction and multiple characterizations. This research demonstrates the feasibility of MoS for Zn-storage anodes that can be used to construct reliable aqueous full batteries.

摘要

可充电水系锌离子电池(AZIBs)因其低成本和高安全性而备受关注,但锌金属阳极的枝晶生长、低电镀/剥离效率、表面钝化和自腐蚀阻碍了它们的应用。在此,提出了一种一步分子工程策略,用于同时构建具有扩大层间距、氧掺杂、结构缺陷和丰富1T相的分级MoS双层纳米管(MoS-DLTs),将其设计为“摇椅式”AZIBs的嵌入型阳极,避免了锌阳极问题,因此展现出长循环寿命。受益于结构优化和分子工程,MoS-DLTs的锌扩散效率和界面反应动力学得到增强。当与自制的ZnMnO阴极耦合时,组装的MoS-DLTs//ZnMnO全电池表现出令人印象深刻的循环稳定性,在1 A g下10000次循环后容量保持率为86.6%,优于大多数已报道的“摇椅式”AZIBs。通过同步辐射粉末X射线衍射和多种表征手段研究了MoS-DLTs的Zn/H共嵌入机制。这项研究证明了MoS作为锌存储阳极用于构建可靠水系全电池的可行性。

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