TY - JOUR
T1 - In-situ forming lithiophilic-lithiophobic gradient interphases for dendrite-free all-solid-state Li metal batteries
AU - Lin, Yanke
AU - Wang, Tianshuai
AU - Zhang, Leicheng
AU - Peng, Xudong
AU - Huang, Baoling
AU - Wu, Maochun
AU - Zhao, Tianshou
N1 - Funding Information:
The work described in this paper was fully supported by a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. R6005–20, HKUST).
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/8
Y1 - 2022/8
N2 - Solid polymer electrolytes offer a promise for all-solid-state Li batteries due to their low cost and good processability. However, dendrites and the associated contact loss occurring at the undesirable Li/electrolyte interface during repeated plating and stripping remain a challenge. To address the issue, here, we propose to coat a thin layer containing Al/Li dual-salt onto the polyethylene oxide (PEO) electrolyte. When cycled with the Li metal anode, the salts are sequentially reduced, in-situ forming a lithiophilic Li-Al alloy-rich layer near the anode and a lithiophobic LiF-rich layer close to the electrolyte. The former improves the interfacial adhesion and regulates the Li nucleation, while the latter contributes to dendrite suppression due to its high interface energy against Li. As a result, the gradient interphase enables a Li/Li symmetrical cell to be stably cycled for over 1000 h without short circuits. Moreover, the full cell paired with the LiFePO4 cathode shows enhanced cyclability, retaining 89.1% capacity after 350 cycles at 0.5 C. A pouch cell using the dual-salt coated electrolyte demonstrates good performance and safety. This work provides a facile yet effective approach to construct functional interphase for achieving stable batteries using solid polymer electrolytes.
AB - Solid polymer electrolytes offer a promise for all-solid-state Li batteries due to their low cost and good processability. However, dendrites and the associated contact loss occurring at the undesirable Li/electrolyte interface during repeated plating and stripping remain a challenge. To address the issue, here, we propose to coat a thin layer containing Al/Li dual-salt onto the polyethylene oxide (PEO) electrolyte. When cycled with the Li metal anode, the salts are sequentially reduced, in-situ forming a lithiophilic Li-Al alloy-rich layer near the anode and a lithiophobic LiF-rich layer close to the electrolyte. The former improves the interfacial adhesion and regulates the Li nucleation, while the latter contributes to dendrite suppression due to its high interface energy against Li. As a result, the gradient interphase enables a Li/Li symmetrical cell to be stably cycled for over 1000 h without short circuits. Moreover, the full cell paired with the LiFePO4 cathode shows enhanced cyclability, retaining 89.1% capacity after 350 cycles at 0.5 C. A pouch cell using the dual-salt coated electrolyte demonstrates good performance and safety. This work provides a facile yet effective approach to construct functional interphase for achieving stable batteries using solid polymer electrolytes.
KW - All-solid-state battery
KW - Solid polymer electrolyte
KW - Li metal anode
KW - Gradient interphase
KW - Interface stability
UR - http://www.scopus.com/inward/record.url?scp=85130938164&partnerID=8YFLogxK
U2 - 10.1016/j.nanoen.2022.107395
DO - 10.1016/j.nanoen.2022.107395
M3 - Journal article
SN - 2211-2855
VL - 99
JO - Nano Energy
JF - Nano Energy
M1 - 107395
ER -