插层(化学)
尖晶石
正交晶系
扩散
离子
阴极
电池(电)
电化学
锂(药物)
铰链
实现(概率)
材料科学
化学物理
化学
结晶学
纳米技术
工程物理
拓扑(电路)
无机化学
电极
电气工程
晶体结构
有机化学
物理
物理化学
热力学
内分泌学
功率(物理)
工程类
冶金
统计
经典力学
医学
数学
作者
Ziqin Rong,Rahul Malik,Pieremanuele Canepa,Gopalakrishnan Sai Gautam,Miao Liu,Anubhav Jain,Kristin Aslaug Persson,Gerbrand Ceder
标识
DOI:10.1021/acs.chemmater.5b02342
摘要
The diffusion of ions in solid materials plays an important role in many aspects of materials science such as the geological evolution of minerals, materials synthesis, and in device performance across several technologies. For example, the realization of multivalent (MV) batteries, which offer a realistic route to superseding the electrochemical performance of Li-ion batteries, hinges on the discovery of host materials that possess adequate mobility of the MV intercalant to support reasonable charge and discharge times. This has proven especially challenging, motivating the current investigation of ion mobility (Li +, Mg 2+, Zn 2+, Ca 2+, and Al 3+ ) in spinel Mn 2 O 4, olivine FePO 4, layered NiO 2, and orthorhombic δ-V 2 O 5 . In this study, we not only quantitatively assess these structures as candidate cathode materials, but also isolate the chemical and structural descriptors that govern MV diffusion. Our finding that matching the intercalant site preference to the diffusion path topology of the host structure controls mobility more than any other factor leads to practical and implementable guidelines to find fast-diffusing MV ion conductors.
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