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通过卤化TiC MXenes实现晶格匹配和卤素调控以协同诱导均匀锌电沉积

Lattice Matching and Halogen Regulation for Synergistically Induced Uniform Zinc Electrodeposition by Halogenated TiC MXenes.

作者信息

Li Xinliang, Li Mian, Luo Kan, Hou Yue, Li Pei, Yang Qi, Huang Zhaodong, Liang Guojin, Chen Ze, Du Shiyu, Huang Qing, Zhi Chunyi

机构信息

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China.

Engineering Laboratory of Advanced Energy Materials, Ningbo Institute of Materials Technology& Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201, China.

出版信息

ACS Nano. 2022 Jan 25;16(1):813-822. doi: 10.1021/acsnano.1c08358. Epub 2021 Dec 28.

DOI:10.1021/acsnano.1c08358
PMID:34962775
Abstract

Dendrite growth and low Coulombic efficiency caused by uneven diffusion and electrodeposition of Zn ions have emerged as a barrier to exploit the Zn metal anode. In this work, we demonstrate the stoichiometric halogenated MXenes (TiCCl, TiCBr, and TiCI) as an artificial layer that can induce the uniform Zn deposition. The efficient redistribution effect results from the coherent heterogeneous interface reconstruction and regulated ion tiling by halogen surficial termination. The synergetic effects of high lattice matching (90%) between the adopted MXenes and Zn, as well as the positive halogen regulation, Zn ions are guided to nucleate uniformly on the most extensive () crystal plane of the MXene matrix and grow in a planar manner. In terms of Zn ion regulation, Cl termination is found to be more effective than O/F, Br, and I due to its moderate adsorption and diffusion coefficiency for Zn ions. The TiCCl-Zn anode achieves a life extension of over 12 times (840 h at 2 mA cm//1 mAh cm) over that of the bare Zn anode and serves more than 9000 cycles in a battery with a TiCI cathode at a high rate of 3 A g. Given the abundance of lattice parameters and terminations of MXene materials, the developed strategy is expected to be extended to other metal anode systems.

摘要

锌离子不均匀扩散和电沉积导致的枝晶生长以及低库仑效率,已成为开发锌金属负极的障碍。在这项工作中,我们展示了化学计量比的卤化MXenes(TiCCl、TiCBr和TiCI)作为一种人工层,它可以诱导锌的均匀沉积。这种有效的再分布效应源于由卤素表面端基引起的相干异质界面重构和调控的离子平铺。所采用的MXenes与锌之间的高晶格匹配度(90%)以及正卤素调控的协同效应,引导锌离子在MXene基体最广泛的()晶面上均匀成核并以平面方式生长。在锌离子调控方面,由于其对锌离子具有适度的吸附和扩散系数,发现Cl端基比O/F、Br和I更有效。TiCCl-Zn负极的寿命比裸锌负极延长了12倍以上(在2 mA cm//1 mAh cm下为840小时),并且在以3 A g的高电流密度使用TiCI正极的电池中可循环超过9000次。鉴于MXene材料丰富的晶格参数和端基,预计所开发的策略可扩展到其他金属负极体系。

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