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Research Highlights

November 2013

The Character of a Cathode

Nickel segregation, cation spatial distribution, and tightly integrated phases occur in pristine battery material

x-ray energy-dispersive spectroscopy maps of LMNO cathode
Scientists obtained a definitive view of an LMNO cathode. The X-ray energy-dispersive spectroscopy maps are shown here, which indicate the distribution of manganese and nickel. Enlarge Image. Flier | slide

Results: To prevent fading in a layered lithium cathode that holds promise for heavy duty transportation use, scientists at Pacific Northwest National Laboratory, FEI Company, and Argonne National Laboratory obtained a definitive view of a pristine cathode made of lithium, nickel, manganese, and oxygen. The cathode is known as Li1.2Ni0.2Mn0.6O2 or LMNO. Controversy has encircled this material. Some state it's a solid solution; others, a composite. To address this debate, the team used a suite of instruments and determined the material is a composite with tightly integrated phases where the surface contains higher concentrations of nickel and low concentrations of oxygen and electron-rich manganese.

"If we want to improve the cycle life and capacity of the layered cathode, we must have this type of clarity around the atomic structure and possible cation ordering," said Dr. Nigel Browning, the Chief Science Officer of PNNL's Chemical Imaging Initiative and a microscopy expert who worked on the study.

Why It Matters: Replacing gasoline-powered cars with electric-powered ones could drop U.S. reliance on oil imports by up to 60%, and reduce harmful emissions as much as 45%, depending on the technological mix used. The key is long-lasting, energy-dense batteries. Innovative LMNO cathodes possess high voltage and high specific capacity. Yet, the material is far from ideal. Capacity and voltage fading issues are linked to the cathode's structure during charging and discharging. The team's characterization research provides the foundation necessary for needed discoveries.

"The ever-growing energy demand of information and transportation relies on lithium-ion batteries for power storage, because of their relatively high energy density and design flexibility. We need it better and we need it now, which contributes to the main driving force for creating new materials for energy storage," said Dr. Chongmin Wang, chemical imaging expert at PNNL and lead investigator on this study.

Method: Using a combination of aberration-corrected scanning transmission electron microscopy, X-ray energy-dispersive spectroscopy, electron energy loss spectroscopy, and complementary multi-slice image simulation, the team probed Li1.2Ni0.2Mn0.6O2 nanoparticles. On the particle's surface, they made several discoveries. A surface with a unique structural characteristic is prone to contain a higher concentration of nickel atoms than the core of the particle, while manganese atoms are more prevalent at the core than the surface. Oxygen vacancies on the particle's surface result in manganese atoms having a valence state or electron configuration of +2.2 on the surface, while the manganese at the particle's center is +4.0.

"This finding indicates a big variation in the local stoichiometry," said Dr. Jun Liu, a materials expert who worked on this study and who is also Director of PNNL's Energy Processes and Materials Division.

Finally, each particle contains both of the material's parent phases. The lattice parameter and crystal structure similarity of the layered LiMO2 phase and the layered Li2MO3 phase allow for the structural integration. 

"This detailed characterization allowed us to gain a more complete picture of the material," said Wang. "Clarification of the material's structure -- nanoscale phase separation, cation ordering and oxygen vacancy formation -- will undoubtedly shine a new light on probing how the material behaves during battery performance and will inspire us to improve its functionality via controlled synthesis."

What's Next: The team is now working to understand how the material evolves during charge/discharge cycles.

Acknowledgments:

Sponsors: The research described in this paper is part of the Chemical Imaging Initiative at PNNL. It was conducted under the Laboratory Directed Research and Development Program at PNNL; J.Z. acknowledges the support of the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of DOE, under the Batteries for Advanced Transportation Technologies program; J.L. acknowledges the support of the DOE Office of Basic Energy Sciences, Materials Sciences and Engineering Division. I.B. and K.A. acknowledge the support from DOE's Freedom CAR and Vehicle Technologies Office.  

User Facilities: Environmental Molecular Sciences Laboratory and National Center for Electron Microscopy

Research Area: Materials Science

Research Team: Meng Gu, Suntharampillai Thevuthasan, Donald R. Baer, Ji-Guang Zhang, Nigel D. Browning, Jun Liu, and Chongmin Wang, Pacific Northwest National Laboratory; Arda Genc, FEI Company; Ilias Belharouak, Dapeng Wang, and Khalil Amine, Argonne National Laboratory

Reference: Gu M, A Genc, I Belharouak, D Wang, K Amine, S Thevuthasan, DR Baer, JG Zhang, ND Browning, J Liu, and C Wang. 2013. "Nanoscale Phase Separation, Cation Ordering, and Surface Chemistry in Pristine Li1.2Ni0.2Mn0.6O2 for Li-Ion Batteries." Chemistry of Materials 25(11):2319-2326. DOI: 10.1021/cm4009392


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