TY - JOUR
T1 - Improving lithium deposition in porous electrodes
T2 - Phase field simulation
AU - Chen, Huiyi
AU - Lin, Chengye
AU - Li, Shu
AU - Liu, Huiyu
AU - Ji, Xiao
AU - Song, Shaojie
AU - Liu, Feng
AU - Chen, Minghua
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/8/1
Y1 - 2024/8/1
N2 - The development of structured lithium metal anodes is a key area of focus in the field of lithium battery research, which can significantly improve the energy density, cycle life and safety of lithium metal batteries. In this study, an electrochemical phase field model is used to construct the total free energy of the electrochemical system in conjunction with the effect of the porous electrode scaffold. It investigates the anisotropy of the diffusion coefficient of lithium ions in the electrolyte and the effect of the gradient size of the porous electrode scaffolds on the lithium deposition within the pores. Our numerical results show that increasing the diffusion coefficient of lithium ions in the x-direction cannot improve the lithium deposition within the pores. Instead, it leads to the appearance of lithium dendrites in the top layer of the porous electrode. Appropriately increasing the diffusion coefficient of lithium ions in the y-direction can significantly increase the lithium deposition capacity within the pores. However, excessive increases can lead to a reversal of the lithium deposition capacity within the pores. In addition, adopting the gradient size of the porous electrode scaffold in the y-direction can effectively alleviate the phenomenon that lithium metal is preferentially deposited at the top of the scaffold. These findings provide new ideas for the future design of structured lithium metal anode batteries.
AB - The development of structured lithium metal anodes is a key area of focus in the field of lithium battery research, which can significantly improve the energy density, cycle life and safety of lithium metal batteries. In this study, an electrochemical phase field model is used to construct the total free energy of the electrochemical system in conjunction with the effect of the porous electrode scaffold. It investigates the anisotropy of the diffusion coefficient of lithium ions in the electrolyte and the effect of the gradient size of the porous electrode scaffolds on the lithium deposition within the pores. Our numerical results show that increasing the diffusion coefficient of lithium ions in the x-direction cannot improve the lithium deposition within the pores. Instead, it leads to the appearance of lithium dendrites in the top layer of the porous electrode. Appropriately increasing the diffusion coefficient of lithium ions in the y-direction can significantly increase the lithium deposition capacity within the pores. However, excessive increases can lead to a reversal of the lithium deposition capacity within the pores. In addition, adopting the gradient size of the porous electrode scaffold in the y-direction can effectively alleviate the phenomenon that lithium metal is preferentially deposited at the top of the scaffold. These findings provide new ideas for the future design of structured lithium metal anode batteries.
KW - Anisotropy
KW - Lithium deposition
KW - Phase-field simulation
KW - Structured lithium metal anode
UR - http://www.scopus.com/inward/record.url?scp=85196495461&partnerID=8YFLogxK
U2 - 10.1016/j.est.2024.112606
DO - 10.1016/j.est.2024.112606
M3 - 文章
AN - SCOPUS:85196495461
SN - 2352-152X
VL - 95
JO - Journal of Energy Storage
JF - Journal of Energy Storage
M1 - 112606
ER -