Bai Wei, Gao Jingyu, Li Kun, Wang Gongrui, Zhou Tengfei, Li Pengju, Qin Shengyong, Zhang Genqiang, Guo Zaiping, Xiao Chong, Xie Yi
Hefei National Laboratory for Physical Sciences at the Microscale, CAS Center for Excellence in Nanoscience, iCHEM, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, Anhui, 230026, P. R. China.
Angew Chem Int Ed Engl. 2020 Sep 28;59(40):17494-17498. doi: 10.1002/anie.202008197. Epub 2020 Aug 11.
Volume expansion and poor conductivity are two major obstacles that hinder the pursuit of the lithium-ion batteries with long cycling life and high power density. Herein, we highlight a misfit compound PbNbS with a soft/rigid superlattice structure, confirmed by scanning tunneling microscopy and electrochemical characterization, as a promising anode material for high performance lithium-ion batteries with optimized capacity, stability, and conductivity. The soft PbS sublayers primarily react with lithium, endowing capacity and preventing decomposition of the superlattice structure, while the rigid NbS sublayers support the skeleton and enhance the migration of electrons and lithium ions, as a result leading to a specific capacity of 710 mAh g at 100 mA g , which is 1.6 times of NbS and 3.9 times of PbS. Our finding reveals the competitive strategy of soft/rigid structure in lithium-ion batteries and broadens the horizons of single-phase anode material design.