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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Ion–Solvent Interplay in Concentrated Electrolytes Enables Subzero Temperature Li-Ion Battery Operations
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Influence of Inorganic Glass Ceramic Particles on Ion States and Ion Transport in Composite Single-I
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Ion Transport and the True Transference Number in Nonaqueous Polyelectrolyte Solutions for Lithium Ion Batteries
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Tuning the Solvation Structure in Aqueous Zinc Batteries to Maximize Zn-Ion Intercalation and Optimize Dendrite-Free Zinc Plating
Aqueous zinc batteries are recognized to suffer from H + /Zn 2+ coinsertion in the cathode, but few approaches have been reported to suppress deleterious H + intercalation. We realize this goal by tuning the solvation structure, using LiV 2 (PO 4 ) 3 (LVP) as a model cathode. Phase conversion of LVP induced by H + intercalation is observed in 4 m Zn(OTf) 2 , whereas dominant Zn 2+ insertion is confirmed in a ZnCl 2 water-in-salt electrolyte (WiSE). This disparity is ascribed to the complete absence of free water and a strong Zn 2+ –H 2 O interaction in the latter that interrupts the H 2 O hydrogen bonding network, thus suppressing H + intercalation. On the basis of this strategy, a novel PEG-based hybrid electrolyte is designed to replace the corrosive ZnCl2 WiSE. This system exhibits an optimized Zn 2+ solvation sheath with a similar low free water content, showing not only much better suppression of H + intercalation but also highly reversible Zn plating/stripping with a CE of ~99.7% over 150 cycles.
Electrostatics of Nanoparticle–Wall Interactions within Nanochannels: Role of Double-Layer Structure and Ion–Ion Correlations
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Reaction Mechanism of the Sn2Fe Anode in Lithium-Ion Batteries
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Conjugated Polymer Energy Level Shifts in Lithium-Ion Battery Electrolytes
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Layered Molybdenum (Oxy)Pyrophosphate as Cathode for Lithium-Ion Batteries
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Nanoscale Investigation of Solid Electrolyte Interphase Inhibition on Li-ion Battery MnO Electrodes via Atomic Layer Deposition of Al2O3
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Integrated Nano-Domains of Disordered and Ordered Spinel Phases in LiNi 0.5 Mn 1.5 O 4 for Li-Ion Batteries
Recent calculations and experimental data suggest that understanding the local ordering behavior of Ni/Mn will be critical to optimize the electrochemical properties of LiNi 0.5 Mn 1.5 O 4 (LNMO) high voltage spinel. In this study, we systematically controlled the evolution of Ni and Mn ordering in LNMO samples by annealing them at 700 °C in air for different dwelling times, followed by quenching to room temperature. The long- and short-range ordering behavior of Ni and Mn were analyzed by combining neutron powder diffraction, X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FT-IR) data. The results show that the fraction of ordered phase increases rapidly during initial annealing at 700 °C for 6 h, and accompanied by decreasing amounts of secondary phases. Annealing longer than 6 h led to the growth in size of ordered domains (i.e., increased segregation of ordered and disordered domains) along with a slow increase in the fraction of ordered phase. The dependence of open circuit voltages (OCVs) of the LNMO on the degree of ordering agrees well with recent calculations using the density functional theory. The increase in the degree of ordering increases the open circuit voltage (OCV) and the initial capacity but reduces cycle life and rate capability. The LNMO delivered optimal battery performances (capacity, cycle life, and rate capability) after annealing at 700 °C for 2 h. This partially ordered sample showed the respective advantages from both disordered and ordered spinels: better spinel-phase purity (thus, higher initial capacity) from the ordered LNMO and better cycle life and rate capability from the disordered LNMO.
Modeling the Partial Atomic Charges in Inorganometallic Molecules and Solids and Charge Redistribution in Lithium-Ion Cathodes
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Counting the Number of Magnesium Ions Bound to the Surface-Immobilized Thymine Oligonucleotides That Comprise Spherical Nucleic Acids
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Stacking Faults Assist Lithium-Ion Conduction in a Halide-Based Superionic Conductor
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Oxide Acidity Modulates Structural Transformations in Hydrogen Titanates during Electrochemical Li-Ion Insertion
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