A Novel Codoping Approach for Enhancing the Performance of LiFePO4 Cathodes

被引:84
作者
Ban, Chunmei [1 ]
Yin, Wan-Jian [2 ]
Tang, Houwen [1 ]
Wei, Su-Huai [1 ]
Yan, Yanfa [2 ]
Dillon, Anne C. [1 ]
机构
[1] Natl Renewable Energy Lab, Golden, CO 80401 USA
[2] Univ Toledo, Dept Phys & Astron, Toledo, OH 43606 USA
关键词
lithium ion batteries; olivine structure; codoping; density-functional theory; TOTAL-ENERGY CALCULATIONS; LITHIUM IRON PHOSPHATE; ALIOVALENT SUBSTITUTIONS; CARBON; IMPACT;
D O I
10.1002/aenm.201200085
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
By combining experimental and theoretical studies, we have demonstrated that donor-acceptor charge-compensating codoping is a promising approach to significantly enhance the rate performance of LiFePO4 cathodes. Our density-functional theory calculation predicts that codoping with Si on the P site and F on the O site modifies the nature of the conduction band edge of LiFePO4 from localized Fe 3d derived states to more delocalized F s and cation s derived states. This effect, thus changes the carrier transport from a poloron-like to a band-like mechanism, and consequently leads to significant improvement in the electrical conductivity of LiFePO4. Most importantly, our comparative doping experiments show that the electrical conductivity of Si P -FO codoped LiFePO4 exhibits at least 2 to 3 orders of magnitude increase in electrical conductivity as compared to that of un-doped LiFePO4. Because of the dramatic improvement of electrical conductivity, the optimal Si-F codoped LiFePO4 shows both a much higher rate-capability than un-doped LiFePO4 or LiFePO4 solely doped with either Si or F. Furthermore, we also believe that the charge-compensating codoping approach may be employed to improve the performance of other cathode materials suffering from inferior electrical conductivities due to localized conduction band states.
引用
收藏
页码:1028 / 1032
页数:5
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