Meng Xin-Hai, Xiao Dongdong, Zhou Zi-Yi, Liu Wen-Zhe, Shi Ji-Lei, Wan Li-Jun, Guo Yu-Guo
CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P.R. China.
University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
J Am Chem Soc. 2024 May 29;146(21):14889-14897. doi: 10.1021/jacs.4c04756. Epub 2024 May 15.
Ni-rich cathodes are some of the most promising candidates for advanced lithium-ion batteries, but their available capacities have been stagnant due to the intrinsic Li storage sites. Extending the voltage window down can induce the phase transition from O3 to 1T of LiNiO-derived cathodes to accommodate excess Li and dramatically increase the capacity. By setting the discharge cutoff voltage of LiNiCoMnO to 1.4 V, we can reach an extremely high capacity of 393 mAh g and an energy density of 1070 Wh kg here. However, the phase transition causes fast capacity decay and related structural evolution is rarely understood, hindering the utilization of this feature. We find that the overlithiated phase transition is self-limiting, which will transform into solid-solution reaction with cycling and make the cathode degradation slow down. This is attributed to the migration of abundant transition metal ions into lithium layers induced by the overlithiation, allowing the intercalation of overstoichiometric Li into the crystal without the O3 framework change. Based on this, the wide-potential cycling stability is further improved via a facile charge-discharge protocol. This work provides deep insight into the overstoichiometric Li storage behaviors in conventional layered cathodes and opens a new avenue toward high-energy batteries.
富镍阴极是先进锂离子电池最有前景的候选材料之一,但由于其固有的锂存储位点,其可用容量一直停滞不前。降低电压窗口可以诱导LiNiO衍生阴极从O3相转变为1T相,以容纳过量的锂并显著提高容量。通过将LiNiCoMnO的放电截止电压设置为1.4 V,我们在此处可以达到393 mAh g的极高容量和1070 Wh kg的能量密度。然而,相变会导致快速的容量衰减,并且相关的结构演变很少被理解,这阻碍了这一特性的利用。我们发现过锂化相变是自限性的,它会随着循环转变为固溶体反应,从而使阴极降解减缓。这归因于过锂化诱导大量过渡金属离子迁移到锂层中,使得过量化学计量的锂能够嵌入晶体而不改变O3框架。基于此,通过简便的充放电协议进一步提高了宽电位循环稳定性。这项工作深入洞察了传统层状阴极中的过化学计量锂存储行为,并为高能电池开辟了一条新途径。