MnO nanoparticles with cationic defects encapsulated in nitrogen-doped porous carbon for high-performance aqueous zinc-ion batteries

被引:25
作者
Yang, Bo [1 ]
Quan, HaiJia [1 ]
Gao, Jing [1 ]
Wang, ShengHan [1 ,2 ]
Wang, Ning [2 ]
Sun, ChengLin [1 ,2 ]
机构
[1] Jilin Univ, Coll Phys, Coherent Light & Atom & Mol Spect Lab, Changchun 130012, Peoples R China
[2] Jilin Univ, Coll Phys, Key Lab Phys & Technol Adv Batteries, Minist Educ, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
High-capacity cathode; Charge storage mechanism; Manganese oxide; In situ Raman spectroscopy; Zinc-ion batteries; CATHODE MATERIAL; ANODE MATERIAL; HIGH-CAPACITY; STORAGE PERFORMANCE; ENERGY-STORAGE; NANOFIBERS; HYBRID;
D O I
10.1016/j.jallcom.2021.161680
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Manganese oxides are admittedly one of the most promising cathode materials in aqueous zinc-ion batteries (ZIBs) because of high operating voltage and economic benefit. However, the design of manganese oxides with high capacity and excellent cycling stability remains challenging. Herein, MnO nanoparticles with cationic defects encapsulated into nitrogen-doped porous carbon (MnO-NC) are synthesized as cathode material for aqueous ZIBs. Benefiting from nitrogen-doping porous carbon improving the electrical conductivity of MnO nanoparticles, MnO-NC exhibits high specific capacity of 402.4 mA h g(-1) at 100 mA g(-1) and long-term cyclic stability up to 1000 cycles at 1000 mA g(-1). The cationic defects in the MnO-NC nanoparticles are also confirmed by XPS analysis, which will facilitate the reversible phase change during cycling. In addition, the ion storage mechanism of MnO-NC cathode is revealed by using XRD, SEM, XPS and in situ Raman spectroscopy, suggesting that the excellent electrochemical behavior of MnO-NC is attributed to the irreversible phase transformation of partial MnO into a layered-type MnO2. These findings demonstrate that porous MnO-NC nanoparticle is a promising cathode material for aqueous ZIBs. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:9
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