假电容
材料科学
阴极
插层(化学)
普鲁士蓝
水溶液
钾离子电池
储能
阳极
无机化学
超级电容器
电极
钾
化学工程
电化学
冶金
磷酸钒锂电池
物理化学
化学
功率(物理)
工程类
物理
量子力学
作者
Meng Huang,Xuanpeng Wang,Jiashen Meng,Xiong Liu,Xuhui Yao,Ziang Liu,Liqiang Mai
出处
期刊:Nano Energy
[Elsevier BV]
日期:2020-07-09
卷期号:77: 105069-105069
被引量:48
标识
DOI:10.1016/j.nanoen.2020.105069
摘要
The intrinsically limited rate capability of batteries by the diffusion-controlled ionic storage mechanism is still existing, and long-service batteries are always required for low-cost grid-scale energy storage. Herein, we design and construct a series of NixZnyHCF (x + y = 3, x = 1, 1.5 or 2) bimetallic Prussian blue analogues as cathode materials for aqueous potassium-ion batteries. On the basis of electrochemical and structural analysis, a synergistic effect between stable Ni2+ and high-voltage Zn2+ in Ni2Zn1HCF is demonstrated, which simultaneously promises ultrafast near-pseudocapacitance intercalation and super-stable potassium storage. As presented, Ni2Zn1HCF cathode shows an extraordinary high-rate capability of 1000C with a capacity retention of 66% and a high capacity recovery of 95.3%, which derives from the large sufeace area and fast near-pseudocapacitive intercalation mechanism. When cycled at 1000C for 80,000 times, a negligible capacity decay of 0.000385% per cycle further proves this cathode to be high-rate and ultra-stable. In addition, the highly reversible solid-solution K+ intercalation/extraction mechanism in the Ni2Zn1HCF cathode is illustrated by the in-situ X-ray diffraction. This work presents a promising cathode for building ultrafast and long-service aqueous potassium-ion batteries.
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