High-performance aqueous Zn-MnO2 batteries enabled by the coupling engineering of K+ pre-intercalation and oxygen defects

被引:57
|
作者
Han, Kun [1 ]
An, Fuqiang [1 ]
Yan, Fengsheng [1 ]
Chen, Hailong [2 ]
Wan, Qi [3 ]
Liu, Yongchang [1 ]
Li, Ping [1 ]
Qu, Xuanhui [1 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China
[2] Georgia Inst Technol, Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[3] Southwest Univ Sci & Technol, Sch Mat Sci & Engn, Mianyang 621010, Sichuan, Peoples R China
基金
北京市自然科学基金;
关键词
ION; TRANSFORMATION; NANOSHEETS; CHEMISTRY; CAPACITY; STORAGE; POINTS;
D O I
10.1039/d1ta03994f
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
Aqueous zinc-manganese dioxide (Zn-MnO2) batteries show great promise for grid-scale energy storage but suffer from sluggish reaction kinetics and severe structural instability of the MnO2 cathode. Herein, a K+-pre-intercalated alpha-MnO2 cathode with oxygen defects (KMOd) is designed, guided by a new coupling engineering strategy, demonstrating boosted reaction kinetics and improved structural stability of MnO2. Closely coupled first-principles calculations and experiments reveal that the synergy effects of pre-intercalated K+ and oxygen defects are key to the high electronic conductivity, favorable H+ diffusion kinetics, enhanced H+/Zn2+ adsorption/intercalation capability, and improved structural stability of the KMOd cathode. A high energy density of 518 W h kg(-1) calculated based on the mass of the cathode and outstanding long-term cycling performance of over 2500 cycles at 2.0 A g(-1) with a capacity of 203 mA h g(-1) and a retention of 81.3% are achieved. New insights into the structural stabilization effect by adding K2SO4 additive into the aqueous electrolyte are also revealed. A hybrid charge storage mechanism of non-diffusion controlled Zn2+ intercalation and diffusion controlled H+ intercalation is proposed.
引用
收藏
页码:15637 / 15647
页数:11
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