Shen Yabin, Yin Dongming, Xue Hongjin, Sun Wei, Wang Limin, Cheng Yong
Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450002, China.
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
J Colloid Interface Sci. 2024 Jun;663:961-970. doi: 10.1016/j.jcis.2024.02.213. Epub 2024 Mar 2.
High-voltage medium-nickel low-cobalt lithium layered oxide cathode materials are intriguing for lithium-ion batteries (LIBs) applications because of their relatively low cost and high capacity. Unfortunately, high charging voltage induces bulk layered structure decline and interface environment deterioration, low cobalt content reduces lithium diffusion kinetics, severely limiting the performance liberation of this kind of cathode. Here, a multifunctional Al/Zr dual cation doping strategy is employed to enhance the electrochemical performance of LiNiCoMnO (NCM) cathode at a high charging cut-off voltage of 4.5 V. On the one hand, Al/Zr co-doping weakens the Li/Ni mixing through magnetic interactions due to the inexistence of unpaired electrons for Al and Zr, thereby increasing the lithium diffusion rate and suppressing the harmful coexistence of H1 and H2 phases. On the other hand, they enhance the lattice oxygen framework stability due to strong Al-O and Zr-O bonds, inhibiting the undesired H2 to H3 phase transition and interface lattice oxygen loss, thereby enhancing the stability of the bulk structure and cathode-electrolyte interface. As a result, Al/Zr co-doped NCM (NCMAZ) shows a 94.2 % capacity retention rate after 100 cycles, while that of NCM is only 79.4 %. NCMAZ also exhibits better rate performance than NCM, with output capacities of 92 mAh/g and 59 mAh/g at a high current density of 5C, respectively. The modification strategy will make the high-voltage medium-nickel low-cobalt cathode closer to practical applications.
高压中镍低钴锂层状氧化物阴极材料因其相对较低的成本和高容量而在锂离子电池(LIBs)应用中备受关注。不幸的是,高充电电压会导致体相层状结构衰退和界面环境恶化,低钴含量会降低锂扩散动力学,严重限制了这类阴极的性能释放。在此,采用多功能Al/Zr双阳离子掺杂策略来提高LiNiCoMnO(NCM)阴极在4.5 V高充电截止电压下的电化学性能。一方面,由于Al和Zr不存在未成对电子,Al/Zr共掺杂通过磁相互作用减弱了Li/Ni混合,从而提高了锂扩散速率并抑制了H1和H2相的有害共存。另一方面,由于强Al-O和Zr-O键,它们增强了晶格氧框架稳定性,抑制了不期望的H2到H3相转变和界面晶格氧损失,从而提高了体相结构和阴极-电解质界面的稳定性。结果,Al/Zr共掺杂的NCM(NCMAZ)在100次循环后显示出94.2%的容量保持率,而NCM仅为79.4%。NCMAZ在倍率性能方面也优于NCM,在5C的高电流密度下输出容量分别为92 mAh/g和59 mAh/g。该改性策略将使高压中镍低钴阴极更接近实际应用。