Cointercalation of Polyaniline and Alkali-Earth Cations into V2O5 to Boost Aqueous Zinc-Ion Storage Performance with Superior Cycling Stability

被引:2
|
作者
Su, Zhou [1 ]
Zhao, Mingshu [1 ]
Jiao, Lidong [1 ]
Shi, Mangmang [1 ]
Li, Min [1 ]
Li, Feng [1 ]
Wang, Qiuwen [1 ]
Zhu, Hongchuan [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Phys, Key Lab Shaanxi Adv Funct Mat & Mesoscop Phys, MOE Key Lab Nonequilibrium Synth & Modulat Condens, Xian 710049, Shaanxi, Peoples R China
关键词
ELECTROCHEMICAL ENERGY-STORAGE; CATHODE; INTERCALATION; ELECTROLYTE; BATTERIES; VANADATE; SALT;
D O I
10.1021/acs.energyfuels.4c01189
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Aqueous zinc-ion batteries (AZIBs) are considered as an attractive alternative to lithium-ion batteries. Although the vanadium pentoxide (V2O5) cathode exhibits high theoretical capacity of 589 mA h g(-1) for zinc-storage, it suffers from capacity decay and sluggish Zn2+ diffusion kinetics due to the strong electrostatic interactions with Zn2+, slight dissolution in aqueous electrolytes, and low electronic conductivity. Herein, the polyaniline and alkali-earth cation (Mg2+, Ca2+) cointercalated V2O5 composites (PVO-Mg, PVO-Ca) are fabricated to boost the zinc ion storage performance of vanadium oxide cathodes. PVO-Mg exhibits an enlarged interlayer distance of 14.15 & Aring; and a tremelliform nanoarchitecture composed of nanosheets. The intercalated polyaniline and alkali-earth cations not only expand the Zn2+ diffusion channels but also form a pillar net which can improve the structural stability and electronic conductivity of the layered structure, contributing to superior electrochemical kinetics, interfacial kinetics, and Zn2+ diffusion kinetics. Moreover, ex situ X-ray diffraction results of PVO-Mg show a nearly constant interlayer distance during the insertion and extraction of Zn2+, which indicates that polyaniline and Mg2+ firmly support the layered framework and prevent the expansion and contraction of the interlayer distance. Ex situ X-ray photoelectron spectroscopy results of PVO-Mg reveal the highly reversible formations of Zn-x(CF3SO3)(y)(OH)(2x-y)<middle dot>nH(2)O on the electrode surface and Zn2+ inserted PVO-Mg inside the electrode, as well as a H+ and Zn2+ insertion/extraction process during which the polyaniline serves as a H+ reservoir and a capacity contributor. Consequently, the PVO-Mg electrode exhibits high capacity (387.0 mA h g(-1) at 0.5 A g(-1)), ultrafast rate capability (199.3 mA h g(-1) at 30 A g(-1)), improved cycling stability, and high reversibility and would be a promising cathode for high performance AZIBs.
引用
收藏
页码:10298 / 10309
页数:12
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