Engineering Particle Size for Multivalent Ion Intercalation: Implications for Ion Battery Systems

被引:1
作者
Chen, Wenxiang [1 ,2 ]
Tang, Zhichu [1 ]
Chen, Qian [1 ,3 ,4 ]
机构
[1] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Mat Res Lab, Urbana, IL 61801 USA
[3] Univ Illinois, Mat Res Lab, Dept Chem, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
multivalent ion batteries; particle size effect; solid-solution phase transition; spinel cathodes; reaction mechanism; scanning transmission electron microscopy; CATHODE MATERIALS; SOLID-SOLUTION; LITHIUM; LIMN2O4; OXIDE; MECHANISMS; TRANSITION; LIXFEPO4; NANORODS; ZN2+;
D O I
10.1021/acsanm.1c04360
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Here we present our recent understandings and engineering opportunities on the two-faceted nature of the size effect of cathode particles on electrochemically driven phase transformation pathways and reaction mechanisms. We have been using spinel lambda-MnO2 particles as a model cathode material and Mgand Zn-ion insertion as our focus of multivalent ion battery systems. We find that small, nanoscale cathode particles consistently favor a solid-solution- type phase transition and uniform ion distribution upon discharge. This phase transformation pathway facilitates fast charge insertion kinetics and mechanical stability compared to the multiphase transition pathway in large, micron-sized particles. Meanwhile, when it comes to the electrochemical reaction mechanism, the cathode particle size effect diverges for different systems. Whereas nanoscale cathode particles exhibit superior discharge capacity and cycling performance for Mg-ion-insertion systems, they suffer from a severe side reaction of Mn dissolution in aqueous Zn-ion batteries. Micron-sized lambda-MnO2 particles instead show enhanced cycling performance for Zn-ion insertion because of decreased side reaction sites per mass and accommodation of an interpenetrating network of amorphous MnOx nanosheets. Regarding the mechanistic understanding of the size effect, we discuss insights provided by high-resolution imaging methods such as scanning transmission electron microscopy and scanning electron diffraction, which are capable of monitoring structural changes in cathode particles upon multivalent ion insertion. Together we highlight the opportunities in both fundamentally understanding the electrochemically driven phase transformation in insertion materials and engineering high-performance electrode materials, not by composition variation but by tailoring of the "size".and potentially the shape, exposed facets, surface chemistry, and mesoscale assemblies.of the cathode particles. The particle size effects are transferrable and have potential applications in both multivalent and monovalent ion batteries.
引用
收藏
页码:5983 / 5992
页数:10
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