Loading…

Impurity-vibrational entropy enables quasi-zero-strain layered oxide cathodes for high-voltage sodium-ion batteries

Layered transition metal oxides based on cationic/anionic redox have gained much attention for high-energy-density sodium ion batteries (SIBs). However, irreversible oxygen activity and unstable crystal structure lead to fast capacity fading and undesired rate performance, limiting its large-scale c...

Full description

Saved in:
Bibliographic Details
Published in:Nano energy 2022-12, Vol.103, p.107765, Article 107765
Main Authors: Ren, Haixia, Zheng, Lumin, Li, Yu, Ni, Qiao, Qian, Ji, Li, Ying, Li, Qiaojun, Liu, Mingquan, Bai, Ying, Weng, Suting, Wang, Xuefeng, Wu, Feng, Wu, Chuan
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Layered transition metal oxides based on cationic/anionic redox have gained much attention for high-energy-density sodium ion batteries (SIBs). However, irreversible oxygen activity and unstable crystal structure lead to fast capacity fading and undesired rate performance, limiting its large-scale commercial application. Based on the solid-state physics theory, here we demonstrate that the electrochemical capability in P2-type Na2/3Ni1/3Mn2/3O2 cathode can be significantly improved when impurity-vibrational entropy is increased by simultaneously constructing surface ZrO2 coating and Zr4+ doping (P2-NaNM@Zr). In-situ and ex-situ X-ray diffraction (XRD) verifies that quasi-zero-strain P2-NaNM@Zr cathode maintains P2 phase structure during the charging/discharging process, achieving an ultra-low volume change (1.18%) upon Na+ entire extraction at a high cut-off voltage of 4.5 V. Besides, according to First-principles calculations, we first investigate that the oxygen vacancy formation energy of P2-NaNM@Zr (−2.11 eV) is higher than that of sample P2-NaNM (−2.61 eV), strongly indicating stable and reversible anionic redox reaction. As a result, P2-NaNM@Zr material reveals highly Na storage performance, retaining 86% capacity retention after 1000 cycles at the rate of 5 C within the voltage range of 2.5 − 4.0 V, delivering reversible capacity of 132 mA h g−1 after 50 cycles within 2.0 − 4.5 V. [Display omitted] •The structure stability and cell capability can be improved by Zr decoration.•NaNM@Zr exhibits an ultra-low volume change of 1.18% upon Na+ entire extraction.•NaNM@Zr has high oxygen vacancy formation energy and stable oxygen redox reaction.
ISSN:2211-2855
DOI:10.1016/j.nanoen.2022.107765