电解质
相间
法拉第效率
金属
阴极
材料科学
分解
化学工程
钠
钾
降级(电信)
化学
无机化学
键裂
电极
吡啶
电化学
部分
过渡金属
氧化还原
容量损失
作者
Minyi Zou,Yuanchang Ye,Yingxia Dong,Haihua Li,Junkai Shi,Bomao Huang,Changhong Li,Pengcheng Xue,Ruirui Zhao,Liang Ma,Junpeng Xie,Qifeng Zheng
摘要
ABSTRACT High‐voltage sodium metal batteries (SMBs) suffer from fast degradation stemming from the interfacial incompatibility between electrolytes and electrodes. In this study, potassium 3‐pyridyltrifluoroborate (KPBF 3 ) is proposed as a dual‐interface electrolyte additive, where the pyridine moiety can effectively modulate the anion's electronic structure, lowering its lowest unoccupied molecular orbital energy level and enhancing its binding affinity for Na + . This promotes the preferential reductive decomposition of PBF 3 − , forming a robust NaF‐rich solid electrolyte interphase that suppresses Na dendrite growth. Simultaneously, the cleavage of B─F bonds facilitates the formation of a thin and uniform NaF‐rich cathode electrolyte interphase (CEI), significantly suppressing electrolyte oxidation and greatly improving the high‐voltage stability. Consequently, Na||Na symmetric cells achieve an ultra‐long cycling life of 6000 h at 5 mA cm −2 , while Na||Cu cells exhibit a high average Coulombic efficiency (ACE) of 99.89%. Moreover, Na||Na 3 V 2 (PO 4 ) 2 F 3 cells demonstrate 90.8% capacity retention over 10000 cycles at 10 C and 4.3 V, and 90.0% retention after 2500 cycles at 4.4 V. Notably, this additive also enables SMBs with a low N/P ratio of 2.65 to deliver a high capacity retention of 88.4% after 1000 cycles.
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