A High Capacity Bilayer Cathode for Aqueous Zn-Ion Batteries

被引:189
作者
Zhu, Kaiyue [1 ]
Wu, Tao [1 ]
Huang, Kevin [1 ]
机构
[1] Univ South Carolina, Dept Mech Engn, Columbia, SC 29201 USA
关键词
aqueous Zn-ion battery; cathode; bilayer rho-type V2O5 structure; Ca2+-Zn2+ ionic exchange; Zn-ion (de)intercalation; INITIO MOLECULAR-DYNAMICS; ENERGY-STORAGE; ZINC; MG; LI; NA; INTERCALATION; CHEMISTRY; TRANSPORT; INSERTION;
D O I
10.1021/acsnano.9b08039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aqueous Zn-ion batteries (ZIBs) are promising candidates for grid-scale energy storage because they are intrinsically safe, cost competitive, and energy intense. However, the development of ZIBs is currently challenged by the performance of cathode materials. Herein, we report on Ca0.67V8O20 center dot 3.5H(2)O (CaVO) nanobelts as a type of ZIB cathode with a discharge capacity of 466 mAh g(-1) (equivalent to an energy density of 345.6 Wh kg(-1)) at 0.1 A g(-1) and a capacity retention rate of 100%, 95%, and 74% at 5.0 A g(-1) for 500, 1000, and 2000 cycles, respectively. Through a combined theoretical and experimental study, we reveal that the outstanding energy and power performances of CaVO are deeply rooted in its Zn2+-transport friendly, bilayer rho-type V2O5 structure, and the structure-derived reversibility in single-phase Zn2+-intercalation/deintercalation process. We also uncover that Ca2+ as a structural stabilizer in CaVO undergoes a fast, performance-harmless ion-exchange with Zn2+ in the electrolyte and the entire Zn2+-intercalation/deintercalation process is accompanied by a counter migration of solvent water. Last, we show that a successful synthesis of CaVO depends critically on pH value of the precursor solution and the structural stability of CaVO is controlled by the co-presence of Ca2+/Zn2+ and structural water.
引用
收藏
页码:14447 / 14458
页数:12
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