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通过多层取向堆叠纳米片暴露{010}活性面用于高性能电容型钠离子氧化物阴极

Exposing {010} Active Facets by Multiple-Layer Oriented Stacking Nanosheets for High-Performance Capacitive Sodium-Ion Oxide Cathode.

作者信息

Xiao Yao, Wang Peng-Fei, Yin Ya-Xia, Zhu Yan-Fang, Niu Yu-Bin, Zhang Xu-Dong, Zhang Jienan, Yu Xiqian, Guo Xiao-Dong, Zhong Ben-He, Guo Yu-Guo

机构信息

College of Chemical Engineering, Sichuan University, Chengdu, 610065, P. R. China.

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS), Beijing, 100190, P. R. China.

出版信息

Adv Mater. 2018 Aug 24:e1803765. doi: 10.1002/adma.201803765.

Abstract

As one of the most promising cathodes for rechargeable sodium-ion batteries (SIBs), O3-type layered transition metal oxides commonly suffer from inevitably complicated phase transitions and sluggish kinetics. Here, a Na[Li Ni Mn Cu Mg ]O cathode material with the exposed {010} active facets by multiple-layer oriented stacking nanosheets is presented. Owing to reasonable geometrical structure design and chemical substitution, the electrode delivers outstanding rate performance (71.8 mAh g and 16.9 kW kg at 50C), remarkable cycling stability (91.9% capacity retention after 600 cycles at 5C), and excellent compatibility with hard carbon anode. Based on the combined analyses of cyclic voltammograms, ex situ X-ray absorption spectroscopy, and operando X-ray diffraction, the reaction mechanisms behind the superior electrochemical performance are clearly articulated. Surprisingly, Ni /Ni and Cu /Cu redox couples are simultaneously involved in the charge compensation with a highly reversible O3-P3 phase transition during charge/discharge process and the Na storage is governed by a capacitive mechanism via quantitative kinetics analysis. This optimal bifunctional regulation strategy may offer new insights into the rational design of high-performance cathode materials for SIBs.

摘要

作为可充电钠离子电池(SIBs)最有前景的阴极材料之一,O3型层状过渡金属氧化物通常不可避免地存在复杂的相变和缓慢的动力学问题。在此,我们展示了一种通过多层取向堆叠纳米片暴露{010}活性面的Na[Li Ni Mn Cu Mg ]O阴极材料。由于合理的几何结构设计和化学取代,该电极展现出出色的倍率性能(50C时为71.8 mAh g和16.9 kW kg)、卓越的循环稳定性(5C下600次循环后容量保持率为91.9%)以及与硬碳阳极的优异兼容性。基于循环伏安图、非原位X射线吸收光谱和原位X射线衍射的综合分析,清晰地阐明了优异电化学性能背后的反应机制。令人惊讶的是,在充放电过程中,Ni /Ni和Cu /Cu氧化还原对同时参与电荷补偿,并伴随着高度可逆的O3-P3相变,通过定量动力学分析表明钠存储受电容机制控制。这种优化的双功能调控策略可能为高性能SIBs阴极材料的合理设计提供新的见解。

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