An aliovalent-substituted inorganic-open-framework anode for high-performance potassium-ion batteries

被引:1
|
作者
He, Cuihong [1 ,2 ,3 ]
Zou, Jingmin [1 ,2 ,3 ]
Sun, Chuan-Fu [2 ,3 ]
Liu, Qin [2 ,3 ]
机构
[1] Fuzhou Univ, Coll Chem, Fuzhou 350108, Fujian, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fujian Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Potassium-ion battery; Inorganic open framework; Anode materials; Aliovalent substitution;
D O I
10.1016/j.matlet.2023.134627
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Potassium-ion batteries have drawn great attention owing to the abundant and low-cost potassium resources. However, the lack of highly reversible K+-storage electrodes remains a key concern, due to the large size of K+ ions. Inorganic-open-framework KTiOPO4-type (KTP) anodes are promising K+-hosts, due to their large interstitial vacancies allowing fast and reversible insertion of K+ ions with low structural evolution. Here, we report a new member in the KTP family, K0.63Cr0.56Ti0.55OPO4 (KCTP), with partial aliovalent substitution. The KCTP exhibits a high specific capacity of 123.4 mAh/g and achieves stable cycle life, over 135 days with 98% capacity retention at 10 mA/g and up to 9.9 months with 81% retention at 20 mA/g. The K+-storage process involves biphasic reaction and solid-solution reaction, with a minor volume change of only 8.06%. This work demonstrates that inorganic open frameworks with aliovalent substitution may open a promising way to design high-performance potassium-ion batteries.
引用
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页数:4
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