Affiliation:
1. Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education) College of Physics Jilin University Changchun 130012 China
2. State Key Laboratory of Intelligent Green Vehicle and Mobility School of Vehicle and Mobility Tsinghua University Beijing 100084 China
3. Research Institute of Chemical Defense Beijing 100191 China
Abstract
AbstractSevere capacity degradation at low temperatures (<−20°С) hampers wide applications of lithium‐ion batteries (LIBs) in consumer electronics and electric vehicles. Existing works are dedicated to electrolyte modification because that electrolyte controls both Li+ transportation and interfacial reaction. However, the efforts on electrolytes are always hard to balance rate performance and low‐temperature capacity due to their high viscosity. Herein, a binary coating layer for Li3V2(PO4)3 cathode material without changing electrolyte formulation is proposed, which significantly improves the high‐rate capability and low‐temperature performance of batteries. YPO4 nanoparticles are in situ formed in the amorphous surface carbon layer under the reaction between Li3V2(PO4)3 and Y(NO3)3 during post‐thermal treatment. The C+YPO4 binary coating reduces the side reactions of Li3V2(PO4)3 at high voltage. In addition, the binary surface coating also improves the interfacial kinetics of the electrode at low temperatures. Benefiting from these advantages, the Li3V2(PO4)3 cathode material can cycle stably at ultra‐high rates up to 50 C. In addition, the capacity retention at −20 and −40 °С are improved to 89.1% and 75.7%, respectively. This binary surface‐coated Li3V2(PO4)3 cathode material shows promising application potential in low‐temperature LIBs.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities of Beijing University of Chemical Technology
Chongqing Postdoctoral Science Foundation
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
4 articles.
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