TY - JOUR
T1 - Nucleation and Growth Mode of Solid Electrolyte Interphase in Li-Ion Batteries
AU - Yao, Yu Xing
AU - Wan, Jing
AU - Liang, Ning Yan
AU - Yan, Chong
AU - Wen, Rui
AU - Zhang, Qiang
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/4/12
Y1 - 2023/4/12
N2 - The solid electrolyte interphase (SEI) is regarded as the most important yet least understood component in Li-ion batteries. Considerable effort has been devoted to unravelling its chemistry, structure, and ion-transport mechanism; however, the nucleation and growth mode of SEI, which underlies all these properties, remains the missing piece. We quantify the growth mode of two representative SEIs on carbonaceous anodes based on classical nucleation theories and in situ atomic force microscopy imaging. The formation of inorganic SEI obeys the mixed 2D/3D growth model and is highly dependent on overpotential, whereby large overpotential favors 2D growth. Organic SEI strictly follows the 2D instantaneous nucleation and growth model regardless of overpotential and enables perfect epitaxial passivation of electrodes. We further demonstrate the use of large current pulses during battery formation to promote 2D inorganic SEI growth and improve capacity retention. These insights offer the potential to tailor desired interphases at the nanoscale for future electrochemical devices.
AB - The solid electrolyte interphase (SEI) is regarded as the most important yet least understood component in Li-ion batteries. Considerable effort has been devoted to unravelling its chemistry, structure, and ion-transport mechanism; however, the nucleation and growth mode of SEI, which underlies all these properties, remains the missing piece. We quantify the growth mode of two representative SEIs on carbonaceous anodes based on classical nucleation theories and in situ atomic force microscopy imaging. The formation of inorganic SEI obeys the mixed 2D/3D growth model and is highly dependent on overpotential, whereby large overpotential favors 2D growth. Organic SEI strictly follows the 2D instantaneous nucleation and growth model regardless of overpotential and enables perfect epitaxial passivation of electrodes. We further demonstrate the use of large current pulses during battery formation to promote 2D inorganic SEI growth and improve capacity retention. These insights offer the potential to tailor desired interphases at the nanoscale for future electrochemical devices.
UR - http://www.scopus.com/inward/record.url?scp=85151370303&partnerID=8YFLogxK
U2 - 10.1021/jacs.2c13878
DO - 10.1021/jacs.2c13878
M3 - Article
C2 - 36988463
AN - SCOPUS:85151370303
SN - 0002-7863
VL - 145
SP - 8001
EP - 8006
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 14
ER -