TY - JOUR
T1 - Tailoring solid-electrolyte interphase and solvation structure for subzero temperature, fast-charging, and long-cycle-life sodium-ion batteries
AU - Tao, Lei
AU - Sittisomwong, Poom
AU - Ma, Bingyuan
AU - Hu, Anyang
AU - Xia, Dawei
AU - Hwang, Sooyeon
AU - Huang, Haibo
AU - Bai, Peng
AU - Lin, Feng
N1 - Publisher Copyright:
© 2022
PY - 2023/1
Y1 - 2023/1
N2 - The sluggish Na+ reaction kinetics with carbon materials limits the fast-charging capability, Coulombic efficiency, and cycle life of sodium-ion batteries, especially at low temperatures. Herein, free-standing carbon nanofiber films, with controllable crystallinity and surface chemistry, are used as a platform to investigate the correlation between Na+ reaction kinetics, storage mechanism, and electrolyte environment. The ion solvation effect and solid-electrolyte interphase (SEI) properties determine the kinetics and storage mechanism. A strong Na+-solvent interaction, such as Na+-diglyme, tends to form a “pseudo-SEI” layer dominated by anion decomposition, enabling fast Na+-solvent co-intercalation kinetics. Tuning the SEI chemistries by pre-cycling in the weakly solvated electrolyte (e.g., ester electrolyte), the intercalation capacity rapidly disappears due to the high energy barrier for Na+ transport. Such mechanistic insights allow us to develop the optimal combination of electrode materials and electrolyte chemistry to achieve high initial Coulombic efficiency, ultra-long cycle life under fast charging, and excellent low-temperature performance.
AB - The sluggish Na+ reaction kinetics with carbon materials limits the fast-charging capability, Coulombic efficiency, and cycle life of sodium-ion batteries, especially at low temperatures. Herein, free-standing carbon nanofiber films, with controllable crystallinity and surface chemistry, are used as a platform to investigate the correlation between Na+ reaction kinetics, storage mechanism, and electrolyte environment. The ion solvation effect and solid-electrolyte interphase (SEI) properties determine the kinetics and storage mechanism. A strong Na+-solvent interaction, such as Na+-diglyme, tends to form a “pseudo-SEI” layer dominated by anion decomposition, enabling fast Na+-solvent co-intercalation kinetics. Tuning the SEI chemistries by pre-cycling in the weakly solvated electrolyte (e.g., ester electrolyte), the intercalation capacity rapidly disappears due to the high energy barrier for Na+ transport. Such mechanistic insights allow us to develop the optimal combination of electrode materials and electrolyte chemistry to achieve high initial Coulombic efficiency, ultra-long cycle life under fast charging, and excellent low-temperature performance.
KW - Carbon materials
KW - Co-intercalation
KW - Fast charging
KW - Low temperature
KW - Pseudo-SEI
UR - https://www.scopus.com/pages/publications/85145665866
U2 - 10.1016/j.ensm.2022.12.042
DO - 10.1016/j.ensm.2022.12.042
M3 - Article
AN - SCOPUS:85145665866
SN - 2405-8297
VL - 55
SP - 826
EP - 835
JO - Energy Storage Materials
JF - Energy Storage Materials
ER -