Yuyu Deng, Peiming Dai, Weibin Fu, Ling Che, Licheng Miao, Chengyu Chen, Lifang Jiao, Ting Jin
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The interfacial synergy effect between Na<sub>2</sub>CO<sub>3</sub> and NaF effectively reduces the Na<sup>+</sup> 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<sup>−1</sup> 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 Na<sub>0.85</sub>Li<sub>0.12</sub>Ni<sub>0.22</sub>Mn<sub>0.66</sub>O<sub>2</sub>||HC full cells exhibit a high discharge capacity of 85 mAh g<sup>−1</sup> at −20 °C (85% of its room-temperature capacity). 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引用次数: 0
摘要
醚基电解质由于其高离子电导率和低溶解能,在低温下工作的钠离子电池(sib)中表现出竞争力。然而,由于钠盐的大量分解,无机组分在内部固体电解质间相(SEI)中积累,阻碍了Na+的相间运输动力学。本文提出了一种在稀醚基电解质中具有显著改善Na+扩散动力学的富NaF/ na2co3异质结构SEI。异质结构通过Na2CO3和NaF/Na2CO3界面提供了额外的Na+运输途径。Na2CO3和NaF之间的界面协同效应有效地降低了Na+扩散能垒,提高了SEI的机械鲁棒性,确保了更便利的相间动力学。因此,硬碳(HC)阳极在- 40°C下具有238 mAh g - 1的高可逆比容量,在- 20°C下具有令人印象印象的循环稳定性,在1℃下循环1800次后容量保持率为89.67%。此外,Na0.85Li0.12Ni0.22Mn0.66O2||HC全电池在- 20°C下具有85 mAh g - 1的高放电容量(其室温容量的85%)。这项工作强调了在低温下工作的sib中具有快速Na+传输动力学的工程SEI的关键作用。
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.
期刊介绍:
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