Dual intercalation of inorganics-organics for synergistically tuning the layer spacing of V2O5•nH2O to boost Zn2+ storage for aqueous zinc-ion batteries

被引:42
作者
Feng, Ziyi [1 ]
Zhang, Yifu [1 ]
Zhao, Yunfeng [1 ]
Sun, Jingjing [1 ]
Liu, Yanyan [1 ]
Jiang, Hanmei [1 ]
Cui, Miao [1 ]
Hu, Tao [1 ]
Meng, Changgong [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
关键词
HYDRATED VANADIUM-OXIDE; HIGH-PERFORMANCE; V2O5; CATHODE; VANADATES; CAPACITY; MECHANISM; CARBON;
D O I
10.1039/d2nr02122f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Possessing a 2D zinc-ion transport channel, layered vanadium oxides have become good candidates as cathode materials for aqueous rechargeable zinc-ion batteries (ARZIBs). Tuning the lamellar structure of vanadium oxides to enhance their zinc-ion storage is a great challenge. In the present study, we proposed and investigated a "co-intercalation mechanism" in which Mg2+ and polyaniline (PANI) were simultaneously intercalated into the layers of hydrated V2O5 (MgVOH/PANI) by a one-step hydrothermal method. Inorganic-organic co-intercalation could tune the layer spacing of VOH, and this combination played a synergistic role in enhancing the zinc-ion storage in MgVOH/PANI. It showed an extremely large layer spacing of 14.2 angstrom, specific capacity of up to 412 mA h g(-1) at 0.1 A g(-1), and the capacity retention rate could reach 98% after 1000 cycles. PANI itself has a zinc-storage capacity, and Mg2+ intercalated with PANI can improve the conductivity of the material and enhance its stability. Further first-principles calculations clearly revealed the structural changes and improved electrochemical performance of vanadium oxides. This method of inorganic and organic co-regulation of the VOH structure opens a new strategy for tuning the lamellar structure of layered materials to boost their electrochemical performances.
引用
收藏
页码:8776 / 8788
页数:13
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