Chen Jun, Chen Hongyi, Zhang Shu, Dai Alvin, Li Tianyi, Mei Yu, Ni Lianshan, Gao Xu, Deng Wentao, Yu Lei, Zou Guoqiang, Hou Hongshuai, Dahbi Mouad, Xu Wenqian, Wen Jianguo, Alami Jones, Liu Tongchao, Amine Khalil, Ji Xiaobo
State Key Laboratory of Powder Metallurgy, College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, China.
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL, 60439, USA.
Adv Mater. 2022 Oct;34(42):e2204845. doi: 10.1002/adma.202204845. Epub 2022 Sep 17.
LiCoO (LCO) is widely applied in today's rechargeable battery markets for consumer electronic devices. However, LCO operations at high voltage are hindered by accelerated structure degradation and electrode/electrolyte interface decomposition. To overcome these challenges, co-modified LCO (defined as CB-Mg-LCO) that couples pillar structures with interface shielding are successfully synthesized for achieving high-energy-density and structurally stable cathode material. Benefitting from the "Mg-pillar" effect, irreversible phase transitions are significantly suppressed and highly reversible Li shuttling is enabled. Interestingly, bonding effects between the interfacial lattice oxygen of CB-Mg-LCO and amorphous Co B coating layer are found to elevate the formation energy of oxygen vacancies, thereby considerably mitigating lattice oxygen loss and inhibiting irreversible phase transformation. Meanwhile, interface shielding effects are also beneficial for mitigating parasitic electrode/electrolyte reactions, subsequent Co dissolution, and ultimately enable a robust electrode/electrolyte interface. As a result, the as-designed CB-Mg-LCO cathode achieves a high capacity and excellent cycle stability with 94.6% capacity retention at an extremely high cut-off voltage of 4.6 V. These findings provide new insights for cathode material modification methods, which serves to guide future cathode material design.
钴酸锂(LCO)在当今消费电子设备的可充电电池市场中得到广泛应用。然而,LCO在高电压下的运行受到结构加速退化和电极/电解质界面分解的阻碍。为了克服这些挑战,成功合成了将柱状结构与界面屏蔽相结合的共改性LCO(定义为CB-Mg-LCO),以实现高能量密度和结构稳定的阴极材料。受益于“Mg柱”效应,不可逆相变得到显著抑制,实现了高度可逆的锂穿梭。有趣的是,发现CB-Mg-LCO的界面晶格氧与非晶态Co B涂层之间的键合效应提高了氧空位的形成能,从而大大减轻了晶格氧损失并抑制了不可逆相变。同时,界面屏蔽效应也有利于减轻寄生电极/电解质反应、随后的Co溶解,并最终形成稳定的电极/电解质界面。结果,所设计的CB-Mg-LCO阴极在4.6 V的极高截止电压下实现了高容量和优异的循环稳定性,容量保持率为94.6%。这些发现为阴极材料改性方法提供了新的见解,有助于指导未来阴极材料的设计。