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脉冲激光沉积制备的(104)取向LiNiMnCoO薄膜阴极中可逆电化学锂离子循环的结构变化及机制

Structural changes and mechanisms of reversible electrochemical lithium-ion cycling in (104) oriented LiNiMnCoO thin film cathodes prepared by pulsed laser deposition.

作者信息

Jaklič Blaž, Žuntar Jan, Tchernychova Elena, Kapun Gregor, Šala Martin, Dominko Robert, Spreitzer Matjaž

机构信息

Advanced Materials Department, Jožef Stefan Institute Jamova cesta 39 1000 Ljubljana Slovenia

Jožef Stefan International Postgraduate School Jamova cesta 39 1000 Ljubljana Slovenia.

出版信息

RSC Adv. 2025 Apr 7;15(14):10787-10800. doi: 10.1039/d4ra08924c. eCollection 2025 Apr 4.

Abstract

This study examines the structural and electrochemical behavior of epitaxial (104) oriented LiNiMnCoO (NMC 111) thin film cathodes prepared by pulsed laser deposition, aiming to elucidate the underlying mechanisms of reversible lithium-ion cycling. The effect of growth parameters on film morphology and crystal structure is thoroughly studied. The surface analysis confirms the oxidation states of transition metal ions to be Ni, Mn and Co. Microstructural analysis reveals twinned domains in the NMC 111 layered structure, which conforms with its 4-domain crystallographic orientation. After NMC 111 thin film is charged to 4.2 V, a change in the local electronic structure of nickel and oxygen ions is observed by electron energy loss spectroscopy as a consequence of nickel oxidation. By utilizing reciprocal space mapping after charging to 4.2 V, a negative unit cell volume change was observed, compensated by an increased mosaic spread of NMC 111 lattice planes. This structural adjustment is reversibly maintained upon discharging to 3.0 V. Based on defined epitaxial structures, the reversible mechanism of lithiation and delithiation in NMC 111 thin films is determined on a structural level, providing detailed insight into its functionality. To address structural instability in the charged state, the electrochemical performance was enhanced by cooling the NMC 111 thin films under high oxygen pressure.

摘要

本研究考察了通过脉冲激光沉积制备的外延(104)取向的LiNiMnCoO(NMC 111)薄膜阴极的结构和电化学行为,旨在阐明可逆锂离子循环的潜在机制。深入研究了生长参数对薄膜形态和晶体结构的影响。表面分析证实了过渡金属离子的氧化态为Ni、Mn和Co。微观结构分析揭示了NMC 111层状结构中的孪晶畴,这与其4畴晶体学取向一致。在将NMC 111薄膜充电至4.2 V后,通过电子能量损失谱观察到镍和氧离子的局部电子结构发生变化,这是镍氧化的结果。在充电至4.2 V后利用倒易空间映射,观察到负的晶胞体积变化,由NMC 111晶格平面增加的镶嵌扩展来补偿。这种结构调整在放电至3.0 V时可逆地保持。基于确定的外延结构,在结构层面确定了NMC 111薄膜中锂化和脱锂的可逆机制,从而深入了解其功能。为了解决充电状态下的结构不稳定性,通过在高氧压下冷却NMC 111薄膜提高了电化学性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32a7/11973892/805c21faf9d0/d4ra08924c-f1.jpg

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