普鲁士蓝
结晶度
材料科学
化学工程
拉曼光谱
离子
纳米技术
电化学
电极
复合材料
光学
物理化学
化学
物理
工程类
有机化学
作者
Mingsheng Qin,Wenhao Ren,Ruixuan Jiang,Qi Li,Xuhui Yao,Shiqi Wang,Ya You,Liqiang Mai
标识
DOI:10.1021/acsami.0c20067
摘要
Prussian blue analogs (PBAs) featuring large interstitial voids and rigid structures are broadly recognized as promising cathode materials for sodium-ion batteries. Nevertheless, the conventionally prepared PBAs inevitably suffer from inferior crystallinity and lattice defects, leading to low specific capacity, poor rate capability, and unsatisfied long-term stability. As the Na+ migration within PBAs is directly dependent on the periodic lattice arrangement, it is of essential significance to improve the crystallinity of PBAs and hence ensure long-range lattice periodicity. Herein, a chemical inhibition strategy is developed to prepare a highly crystallized Prussian blue (Na2Fe4[Fe(CN)6]3), which displays an outstanding rate performance (78 mAh g-1 at 100 C) and long life-span properties (62% capacity retention after 2000 cycles) in sodium storage. Experimental results and kinetic analyses demonstrate the efficient electron transfer and smooth ion diffusion within the bulk phase of highly crystallized Prussian blue. Moreover, in situ X-ray diffraction and in situ Raman spectroscopy results demonstrate the robust crystalline framework and reversible phase transformation between cubic and rhombohedral within the charge-discharge process. This research provides an innovative way to optimize PBAs for advanced rechargeable batteries from the perspective of crystallinity.
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