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通过原子层沉积对富镍FCG NMC和NCA阴极进行改性:防止高压锂离子电池的表面相变

Modification of Ni-Rich FCG NMC and NCA Cathodes by Atomic Layer Deposition: Preventing Surface Phase Transitions for High-Voltage Lithium-Ion Batteries.

作者信息

Mohanty Debasish, Dahlberg Kevin, King David M, David Lamuel A, Sefat Athena S, Wood David L, Daniel Claus, Dhar Subhash, Mahajan Vishal, Lee Myongjai, Albano Fabio

机构信息

Energy and Transportation Science Division, Oak Ridge National Laboratory, Oak Ridge, TN, USA.

Energy Power Systems, LLC, Pontiac, MI, USA.

出版信息

Sci Rep. 2016 May 26;6:26532. doi: 10.1038/srep26532.

DOI:10.1038/srep26532
PMID:27226071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4880920/
Abstract

The energy density of current lithium-ion batteries (LIBs) based on layered LiMO2 cathodes (M = Ni, Mn, Co: NMC; M = Ni, Co, Al: NCA) needs to be improved significantly in order to compete with internal combustion engines and allow for widespread implementation of electric vehicles (EVs). In this report, we show that atomic layer deposition (ALD) of titania (TiO2) and alumina (Al2O3) on Ni-rich FCG NMC and NCA active material particles could substantially improve LIB performance and allow for increased upper cutoff voltage (UCV) during charging, which delivers significantly increased specific energy utilization. Our results show that Al2O3 coating improved the NMC cycling performance by 40% and the NCA cycling performance by 34% at 1 C/-1 C with respectively 4.35 V and 4.4 V UCV in 2 Ah pouch cells. High resolution TEM/SAED structural characterization revealed that Al2O3 coatings prevented surface-initiated layered-to-spinel phase transitions in coated materials which were prevalent in uncoated materials. EIS confirmed that Al2O3-coated materials had significantly lower increase in the charge transfer component of impedance during cycling. The ability to mitigate degradation mechanisms for Ni-rich NMC and NCA illustrated in this report provides insight into a method to enable the performance of high-voltage LIBs.

摘要

为了与内燃机竞争并实现电动汽车(EV)的广泛应用,基于层状LiMO₂阴极(M = Ni、Mn、Co:NMC;M = Ni、Co、Al:NCA)的当前锂离子电池(LIB)的能量密度需要显著提高。在本报告中,我们表明,在富镍FCG NMC和NCA活性材料颗粒上原子层沉积(ALD)二氧化钛(TiO₂)和氧化铝(Al₂O₃)可以显著改善LIB性能,并允许在充电期间提高上限截止电压(UCV),从而显著提高比能量利用率。我们的结果表明,在2 Ah软包电池中,Al₂O₃涂层在1 C/-1 C、UCV分别为4.35 V和4.4 V的条件下,将NMC的循环性能提高了40%,将NCA的循环性能提高了34%。高分辨率TEM/SAED结构表征表明,Al₂O₃涂层可防止涂层材料中发生表面引发的从层状到尖晶石的相变,而这种相变在未涂层材料中很普遍。EIS证实,Al₂O₃涂层材料在循环过程中阻抗的电荷转移分量增加显著更低。本报告中所阐述的减轻富镍NMC和NCA降解机制的能力,为实现高压LIB性能提供了一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/e5f8a69bee85/srep26532-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/7cc2f39e441a/srep26532-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/2bb32accaafe/srep26532-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/9ca43043497d/srep26532-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/2cfc1bf4e11a/srep26532-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/0cc05535f390/srep26532-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/e01ab4a2dd04/srep26532-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/dd4bad83e1d5/srep26532-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/6440713d4da9/srep26532-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/e5f8a69bee85/srep26532-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/7cc2f39e441a/srep26532-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/2bb32accaafe/srep26532-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/9ca43043497d/srep26532-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/2cfc1bf4e11a/srep26532-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/0cc05535f390/srep26532-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/e01ab4a2dd04/srep26532-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/dd4bad83e1d5/srep26532-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/6440713d4da9/srep26532-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a68/4880920/e5f8a69bee85/srep26532-f9.jpg

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