普鲁士蓝
插层(化学)
铵
水溶液
离子
空位缺陷
材料科学
吸收(声学)
化学工程
无机化学
化学
结晶学
物理化学
有机化学
电极
工程类
复合材料
电化学
作者
Fangyu Xiong,Xiaolin Liu,Chunli Zuo,Xiaolin Zhang,Tao Yang,Binbin Zhou,Guobin Zhang,Shuangshuang Tan,Qinyou An,Paul K. Chu
标识
DOI:10.1021/acs.jpclett.3c03579
摘要
Emerging aqueous ammonium-ion batteries (AIBs) are considered inexpensive, highly safe, ecofriendly, and sustainable energy storage systems. Although some high-performance electrode materials have been reported for AIBs, a comprehensive understanding of the origin of the high ammonium-ion storage performance is still lacking. Herein, the percolating network of anionic vacancies is determined to be the origin of the superior ammonium-ion storage properties of the Prussian blue analogues based on ab initio molecular dynamics simulation and electrochemical kinetic analyses. Fe[Fe(CN)6] with a percolating anionic vacancy network delivers an outstanding rate of 64.7 mAh g–1 at 2000 mA g–1 in addition to a capacity retention of 94.5% after 10 000 cycles. The low-strain intercalation ammonium-ion storage mechanism of highly deficient Fe Prussian blue with Fe as the redox center is revealed by in situ X-ray diffraction and ex situ X-ray absorption fine structure analysis. The results provide insights into the mechanism of ammonium-ion storage in Prussian blue analogues and guidance in the development of aqueous AIBs.
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