Haifeng Yu,Zhihua Ren,Zhihong Wang,Hui Sun,Ling Chen,Hao Jiang,Chunzhong Li
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引用次数: 0
摘要
层状富镍无钴阴极在能量密度和成本效益方面具有引人注目的优势,但其实际应用受到结构不稳定性和缓慢的电荷转移动力学的严重阻碍。本文报道了一种尖晶石Li1-xCoO2表面工程的lini0.92 mn0.05 al0.030 o2 (Co- nma)阴极,其Co含量仅为~ 2000 ppm,其中微量Co的有效利用显著提高了结构完整性和界面反应动力学。综合原位/非原位光谱化学分析表明,表面工程有效地抑制了寄生界面反应,在首次充电过程中O2/CO2排放量可以忽略不计。同时,尖晶石Li1-xCoO2促进了更快的Li+扩散和电子转移,从而降低了电化学极化,提高了相变可逆性。因此,Co-NMA在0.1C时具有225.3 mAh g-1的高可逆容量,初始库仑效率为93.4%。即使在10C时,其容量保持率仍为62.1%,大大优于相应的第四纪NMCA(54.2%)和NMA(49.1%)。在袋式全电池中,Co-NMA的循环寿命超过650次,容量保持率为80%,远远超过NMCA(<320次)和目前报道的基于nma的阴极。
Trace-Cobalt Surface Engineering of Ni-Rich Co-Free Cathodes Unlocks High-Power Density and Long-Cycle Life in Pouch-Type Li-Ion Batteries.
Layered Ni-rich Co-free cathodes offer compelling advantages in energy density and cost-effectiveness, but their practical deployment is significantly hindered by structural instability and sluggish charge transfer kinetics. Herein, we report a spinel Li1-xCoO2 surface-engineered LiNi0.92Mn0.05Al0.03O2 (Co-NMA) cathode with only ∼2000 ppm Co, in which the efficient utilization of trace Co dramatically enhances both structural integrity and interfacial reaction kinetics. Comprehensive in/ex situ spectrochemical analyses reveal that surface engineering effectively suppresses parasitic interface reactions with negligible O2/CO2 emission in the first charge process. Concurrently, spinel Li1-xCoO2 facilitates faster Li+ diffusion and electron transfer, resulting in lower electrochemical polarization and higher phase-transition reversibility. Consequently, the Co-NMA delivers a high reversible capacity of 225.3 mAh g-1 at 0.1C and an initial Coulombic efficiency of 93.4%. It retains 62.1% of its capacity retention even at 10C, greatly outperforming the corresponding quaternary NMCA (54.2%) and NMA (49.1%). In pouch-type full cells, the Co-NMA sustains an extended cycle life over 650 cycles with 80% capacity retention, far surpassing NMCA (<320 cycles) and the reported NMA-based cathodes.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.