101 research outputs found
Soft-templating synthesis of mesoporous magnetic CuFe2O4 thin films with ordered 3D honeycomb structure and partially inverted nanocrystalline spinel domains
ChemInform Abstract: Ordered Large-Pore Mesoporous Li4Ti5O12 Spinel Thin Film Electrodes with Nanocrystalline Framework for High Rate Rechargeable Lithium Batteries: Relationships Among Charge Storage, Electrical Conductivity, and Nanoscale Structure.
Nanocrystalline NiMoO4 with an ordered mesoporous morphology as potential material for rechargeable thin film lithium batteries
Mesoporous (M = Co, Cu, Mg, Ni, Zn) Thin Films with Nanocrystalline Walls, Uniform 16 nm Diameter Pores and High Thermal Stability: Template-Directed Synthesis and Characterization of Redox Active Trevorite
Toward ordered mesoporous rare-earth sesquioxide thin films via polymer templating: high temperature stable C-type with finely-tunable crystallite sizes
Nanocrystalline thin film materials with ordered 3D mesoporous and nanopillar-like structures through PIB-b-PEO polymer templating: towards high-performance UV-light photocatalysts
Delayed Thermal Runaway Investigation on Commercial 2.6 Ah NCM-LCO Based 18650 Lithium Ion Cells with Accelerating Rate Calorimetry
The thermal runaway behavior during a nail penetration test of lithium metal oxide based commercially available 18650-type lithium ion cells was investigated regarding the influence of nail design, state of charge (SOC) and state of health (SOH) under quasi-adiabatic conditions. Whether an immediate or a delayed thermal runaway occurs, is highly dependent on the angle of the nail tip. A rather blunt nail provokes a more severe reaction leading to an immediate thermal runaway at 100% SOC. The lower the SOC, the less severe is the cell self-heating. After nail penetration further self-heating causing a thermal runaway is highly dependent on the adjusted SOC. The impacts of aging result to be beneficial for safety down to a SOH of 90%.</jats:p
Influence of temperature on the aging behavior of 18650-type lithium ion cells: A comprehensive approach combining electrochemical characterization and post-mortem analysis
The understanding of the aging behavior of lithium ion batteries in automotive and energy storage applications is essential for the acceptance of the technology. Therefore, aging experiments were conducted on commercial 18650-type state-of-the-art cells to determine the influence of the temperature during electrochemical cycling on the aging behavior of the different cell components. The cells, based on Li(Ni0.5Co0.2Mn0.3)O2 (NCM532)/graphite, were aged at 20 °C and 45 °C to different states of health. The electrochemical performance of the investigated cells shows remarkable differences depending on the cycling temperature. At contrast to the expected behavior, the cells cycled at 45 °C show a better electrochemical performance over lifetime than the cells cycled at 20 °C. Comprehensive post-mortem analyses revealed the main aging mechanisms, showing a complex interaction between electrodes and electrolyte. The main aging mechanisms of the cells cycled at 45 °C differ strongly at contrast to cells cycled at 20 °C. A strong correlation between the formed SEI, the electrolyte composition and the electrochemical performance over lifetime was observed
Facile and General Synthesis of Thermally Stable Ordered Mesoporous Rare-Earth Oxide Ceramic Thin Films with Uniform Mid-Size to Large-Size Pores and Strong Crystalline Texture
We
describe the general synthesis of submicrometer-thick rare-earth/lanthanide
sesquioxide (RE<sub>2</sub>O<sub>3</sub>) films with tailorable pore
and grain sizes via polymer templating of hydrated chloride salt precursors.
Mesostructured RE<sub>2</sub>O<sub>3</sub> (RE = Sm, Tb–Lu)
ceramics with cubic pore symmetry and high surface area (<i>S</i><sub>BET</sub> ≥ 50 m<sup>2</sup> g<sup>–1</sup>) were
prepared using different diblock copolymer structure-directing agents
and were characterized by a combination of electron microscopy, in
situ and ex situ grazing incidence small-angle X-ray scattering, N<sub>2</sub> physisorption, X-ray photoelectron spectroscopy, X-ray diffraction
including Rietveld refinement, and ultraviolet–visible spectroscopy.
In the present work, we specifically focus on Dy<sub>2</sub>O<sub>3</sub> and Yb<sub>2</sub>O<sub>3</sub> and use both of these materials
as model systems to study, among other things, the film formation
and microstructure. Our research data collectively demonstrate that
(1) record pore sizes of up to 42 nm in diameter can be achieved without
the need for swelling agents, (2) the nanostructure can be preserved
up to 1000 °C for the heavier oxides, (3) the sizes of the optical
band gaps (4.9–5.6 eV) are comparable to those reported for
single crystals, (4) the sol–gel-derived materials are single
phase and adopt the <i>C</i>-type crystal structure, and
(5) the grain growth is virtually linear, with domain sizes in the
range of 3–16 nm. We also show that, except for Yb<sub>2</sub>O<sub>3</sub>, all of the samples have a fiber texture and the preferred
orientation is significant in Sm<sub>2</sub>O<sub>3</sub> and Lu<sub>2</sub>O<sub>3</sub> films (March parameter <i>G</i><sub>2</sub> < 0.1). Overall, the synthesis parameters described in
this work provide a blueprint for the preparation of thermally stable
rare-earth oxide ceramics with both a mesoporous morphology and iso-oriented
nanocrystalline walls
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