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Anisotropic Lattice Strain and Mechanical Degradation of High- and Low-Nickel NCM Cathode Materials for Li-Ion Batteries
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作者:

Kondrakov, Aleksandr O.
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Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Schmidt, Alexander
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Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Xu, Jin
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Karlsruhe Inst Technol, Inst Appl Mat, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Gesswein, Holger
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Karlsruhe Inst Technol, Inst Appl Mat, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
Helmholtz Inst Ulm Elect Energy Storage, Helmholtzstr 11, D-89081 Ulm, Germany Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

Moenig, Reiner
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Karlsruhe Inst Technol, Inst Appl Mat, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
Helmholtz Inst Ulm Elect Energy Storage, Helmholtzstr 11, D-89081 Ulm, Germany Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany

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机构:
[1] Karlsruhe Inst Technol, Inst Nanotechnol, Battery & Elect Lab, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[2] Karlsruhe Inst Technol, Inst Appl Mat, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
[3] Helmholtz Inst Ulm Elect Energy Storage, Helmholtzstr 11, D-89081 Ulm, Germany
[4] BASF SE, D-67056 Ludwigshafen, Germany
[5] Justus Liebig Univ Giessen, Inst Phys Chem, Heinrich Buff Ring 17, D-35392 Giessen, Germany
关键词:
ELECTROCHEMICAL MASS-SPECTROMETRY;
ELECTROLYTE INTERFACE;
PHASE-STABILITY;
LITHIUM;
BEHAVIOR;
INTERCALATION;
DIFFRACTION;
PERFORMANCE;
CARBONATE;
VOLTAGE;
D O I:
10.1021/acs.jpcc.6b12885
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
In the near future, the targets for lithiumion batteries concerning specific energy and cost can advantageously be met by introducing layered LiNi CoyMnz02 (NCM) cathode materials with a high Ni content (x > 0.6). Increasing the Ni content allows for the utilization of more lithium at a given cell voltage, thereby improving the specific capacity but at the expense of cycle life. Here, the capacityfading mechanisms of both typical low-Ni NCM (x = 0.33, NCM111) and high-Ni NCM (x = 0.8, NCM811) cathodes are investigated and compared from crystallographic and microstructural viewpoints. In situ X-ray diffraction reveals that the unit cells undergo different volumetric changes of around 1.2 and 5.1% for NCM111 and NCM811, respectively, when cycled between 3.0 and 4.3 V vs Li/Li+. Volume changes for NCM811 are largest for x(Li) < 0.5 because of the severe decrease in interlayer lattice parameter c from 14.467(1) to 14.030(1) A. In agreement, in situ light microscopy reveals that delithiation leads to different volume contractions of the secondaryparticles of (3.3 2.4) and (7.8 1.5)% for NCM111 and NCM811, respectively. And postmortem cross-sectional scanning electron microscopy analysis indicates more significant microcracking in the case of NCM811. Overall, the results establish that the accelerated aging of NCM811 is related to the disintegration of secondary particles caused by intergranular fracture, which is driven by mechanical stress at the interfaces between the primary crystallites.
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页码:3286 / 3294
页数:9
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