Achieving high energy density in all-solid-state lithium batteries will require the design of thick cathodes, and these will need to operate reversibly under normal use conditions. We use high-energy depth-profiling X-ray diffraction to measure the localized lithium content of LiNiMnCoO (NMC111) through the thickness of 110 μm thick composite cathodes. The composite cathodes consisted of NMC111 of varying mass loadings mixed with argyrodite solid electrolyte LiPSCl (LPSC). During cycling at C/10, substantial lithiation gradients developed, and varying the NMC111 loading altered the nature of these gradients. Microstructural analysis and cathode modeling showed this was due to high tortuosities in the cathodes. This was particularly true in the solid electrolyte phase, which experienced a marked increase in tortuosity factor during the initial charge. Our results demonstrate that current distributions are observed in sulfide-based composites and that these will be an important consideration for practical design of all-solid-state batteries.
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http://dx.doi.org/10.1021/acsenergylett.2c02699 | DOI Listing |
Chem Sci
August 2024
College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology Chengdu 610059 Sichuan China
High voltage/high temperature operation aggravates the risk of capacity attenuation and thermal runaway of layered oxide cathodes due to crystal degradation and interfacial instability. A combined strategy of bulk regulation and surface chemistry design is crucial to handle these issues. Here, we present a simultaneous LiWO-coated and gradient W-doped 0.
View Article and Find Full Text PDFACS Omega
July 2024
Faculty of Chemistry, University of Warsaw, Pasteura 1, 02093 Warsaw, Poland.
In this study, we focus on the large-scale ex situ Raman mapping of LiMnO (LMO) electrodes maintained at varying states of charge. A comprehensive statistical analysis has been conducted at an area of ca. 3660 μm on more than 3100 collected spectra for each LMO electrode sample.
View Article and Find Full Text PDFJ Colloid Interface Sci
November 2024
School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Jiaotong University, Xi'an 710049, People's Republic of China. Electronic address:
Silicon is considered as a promising alternative to traditional graphite anode for lithium-ion batteries. Due to the dramatic volume expansion of silicon anode generated from the insertion of Li ions, the binder which can suppress the severe volume change and repeated massive stress impact during cycling is required greatly. Herein, we design a gradient-distributed two-component binder (GE-PAA) to achieve excellent cyclic stability, and reveal the mechanism of high energy dissipative binder stabilized silicon electrodes.
View Article and Find Full Text PDFACS Energy Lett
February 2023
Department of Chemical Engineering, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts02115, United States.
Achieving high energy density in all-solid-state lithium batteries will require the design of thick cathodes, and these will need to operate reversibly under normal use conditions. We use high-energy depth-profiling X-ray diffraction to measure the localized lithium content of LiNiMnCoO (NMC111) through the thickness of 110 μm thick composite cathodes. The composite cathodes consisted of NMC111 of varying mass loadings mixed with argyrodite solid electrolyte LiPSCl (LPSC).
View Article and Find Full Text PDFNat Commun
November 2023
ESRF - The European Synchrotron, 71 Avenue des Martyrs, 38000, Grenoble, France.
Lithiation dynamics and phase transition mechanisms in most battery cathode materials remain poorly understood, because of the challenge in differentiating inter- and intra-particle heterogeneity. In this work, the structural evolution inside LiMnNiO single crystals during electrochemical delithiation is directly resolved with operando X-ray nanodiffraction microscopy. Metastable domains of solid-solution intermediates do not appear associated with the reaction front between the lithiated and delithiated phases, as predicted by current phase transition theory.
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