Hui Xiong1,Pete Barnes1,2,Yuxing Zuo3,Kiev Dixon1,Dewen Hou1,Sungsik Lee4,Justin Connell4,Hua Zhou4,Yuzi Liu4,Paul Davis2,Olivia Maryon1,Shyue Ping Ong3
Boise State University1,Idaho National Laboratory2,University of California, San Diego3,Argonne National Laboratory4
Hui Xiong1,Pete Barnes1,2,Yuxing Zuo3,Kiev Dixon1,Dewen Hou1,Sungsik Lee4,Justin Connell4,Hua Zhou4,Yuzi Liu4,Paul Davis2,Olivia Maryon1,Shyue Ping Ong3
Boise State University1,Idaho National Laboratory2,University of California, San Diego3,Argonne National Laboratory4
Intercalation-type metal oxide electrodes are promising negative electrode materials for safe and stable operation of rechargeable lithium-ion batteries due to the reduced risk of Li plating at low voltages. Nevertheless, lower energy and power density along with cycling instability remain a bottleneck for their implementation, especially for desirable fast charging applications. Recent studies have shown enhanced electrochemical charge storage in metal oxide electrodes that contain intentional structural defects (e.g., vacancies and interstitials). In this talk, we will discuss an electrochemically driven amorphous-to-crystalline (a-to-c) transformation in a nanoporous Nb<sub>2</sub>O<sub>5</sub> material for Li-ion storage. Through integrated experimental and computational study, we elucidated the mechanism of multi-electron transfer reaction in the a-to-c Nb2O5 electrode as well as its enhanced kinetics for Li-ion batteries.