TY - JOUR
T1 - Heterostructured Solid Electrolyte Interphase Enables Facilitated Kinetics for Low-Temperature Sodium-Ion Batteries
AU - Deng, Yuyu
AU - Dai, Peiming
AU - Fu, Weibin
AU - Che, Ling
AU - Miao, Licheng
AU - Chen, Chengyu
AU - Jiao, Lifang
AU - Jin, Ting
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - Ether-based electrolytes demonstrate competitiveness in sodium-ion batteries (SIBs) operating at low temperatures due to their high ionic conductivities and low desolvation energies. However, the accumulation of inorganic components in the inner solid electrolyte interphase (SEI), caused by substantial sodium salt decomposition, impedes the kinetics of Na+ interphasial transport. Here, a NaF/Na2CO3-rich heterostructured SEI, with significantly improved Na+ diffusion kinetics, is proposed in a dilute ether-based electrolyte. The heterostructure provides additional Na+ transport pathways through Na2CO3 and along the NaF/Na2CO3 interface. The interfacial synergy effect between Na2CO3 and NaF effectively reduces the Na+ diffusion energy barrier and improves the mechanical robustness of SEI, ensuring facilitated interphasial kinetics. Consequently, the hard carbon (HC) anode delivers a high reversible specific capacity of 238 mAh g−1 at −40 °C and an impressive cycling stability at −20 °C with a capacity retention of 89.67% after 1800 cycles at 1 C. Additionally, the Na0.85Li0.12Ni0.22Mn0.66O2||HC full cells exhibit a high discharge capacity of 85 mAh g−1 at −20 °C (85% of its room-temperature capacity). This work underscores the critical role of engineering SEI with fast Na+ transport kinetics for SIBs operating under low temperatures.
AB - Ether-based electrolytes demonstrate competitiveness in sodium-ion batteries (SIBs) operating at low temperatures due to their high ionic conductivities and low desolvation energies. However, the accumulation of inorganic components in the inner solid electrolyte interphase (SEI), caused by substantial sodium salt decomposition, impedes the kinetics of Na+ interphasial transport. Here, a NaF/Na2CO3-rich heterostructured SEI, with significantly improved Na+ diffusion kinetics, is proposed in a dilute ether-based electrolyte. The heterostructure provides additional Na+ transport pathways through Na2CO3 and along the NaF/Na2CO3 interface. The interfacial synergy effect between Na2CO3 and NaF effectively reduces the Na+ diffusion energy barrier and improves the mechanical robustness of SEI, ensuring facilitated interphasial kinetics. Consequently, the hard carbon (HC) anode delivers a high reversible specific capacity of 238 mAh g−1 at −40 °C and an impressive cycling stability at −20 °C with a capacity retention of 89.67% after 1800 cycles at 1 C. Additionally, the Na0.85Li0.12Ni0.22Mn0.66O2||HC full cells exhibit a high discharge capacity of 85 mAh g−1 at −20 °C (85% of its room-temperature capacity). This work underscores the critical role of engineering SEI with fast Na+ transport kinetics for SIBs operating under low temperatures.
KW - hard carbon
KW - heterostructure
KW - low-temperature electrolytes
KW - sodium-ion batteries
KW - solid electrolyte interphase
UR - http://www.scopus.com/inward/record.url?scp=105007808635&partnerID=8YFLogxK
U2 - 10.1002/adfm.202502919
DO - 10.1002/adfm.202502919
M3 - 文章
AN - SCOPUS:105007808635
SN - 1616-301X
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -