Feng Wenting, Wei Xinru, Yang Jianhang, Ma Chenyu, Sun Yiming, Han Junwei, Kong Debin, Zhi Linjie
School of Materials Science and Engineering, China University of Petroleum (East China), Qingdao, China.
College of New Energy, China University of Petroleum (East China), Qingdao, China.
Nat Commun. 2024 Aug 12;15(1):6904. doi: 10.1038/s41467-024-51033-1.
Rechargeable sodium-chlorine (Na-Cl) batteries show high theoretical specific energy density and excellent adaptability for extreme environmental applications. However, the reported cycle life is mostly less than 500 cycles, and the understanding of battery failure mechanisms is quite limited. In this work, we demonstrate that the substantially increased voltage polarization plays a critical role in the battery failure. Typically, the passivation on the porous cathode caused by the deposition of insulated sodium chloride (NaCl) is a crucial factor, significantly influencing the three-phase chlorine (NaCl/Na, Cl/Cl) conversion kinetics. Here, a self-depassivation strategy enabled by iodine anion (I)-tuned NaCl deposition was implemented to enhance the chlorine reversibility. The nucleation and growth of NaCl crystals are well balanced through strong coordination of the NaI deposition-dissolution process, achieving depassivation on the cathode and improving the reoxidation efficiency of solid NaCl. Consequently, the resultant Na-Cl battery delivers a super-long cycle life up to 2000 cycles.
可充电钠氯(Na-Cl)电池具有较高的理论比能量密度,并且在极端环境应用中具有出色的适应性。然而,报道的循环寿命大多少于500次循环,并且对电池失效机制的了解相当有限。在这项工作中,我们证明大幅增加的电压极化在电池失效中起关键作用。通常,由绝缘氯化钠(NaCl)沉积引起的多孔阴极上的钝化是一个关键因素,显著影响三相氯(NaCl/Na,Cl/Cl)转化动力学。在此,实施了一种由碘阴离子(I)调节的NaCl沉积实现的自去钝化策略,以提高氯的可逆性。通过NaI沉积-溶解过程的强配位,NaCl晶体的成核和生长得到很好的平衡,实现阴极去钝化并提高固体NaCl的再氧化效率。因此,所得的Na-Cl电池具有长达2000次循环的超长循环寿命。