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Journal ArticleDOI

Relationship between non-stoichiometry and physical properties in LiNiO2

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TLDR
In this paper, the deintercalation process and magnetic properties were clarified for lithium nickel oxides with different sample compositions which were characterized by neutron and X-ray diffraction measurements, and their interactions were discussed on the basis of weak magnetic-field magnetization measurements.
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This article is published in Solid State Ionics.The article was published on 1995-05-01. It has received 224 citations till now. The article focuses on the topics: Lithium & Magnetization.

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Ageing mechanisms in lithium-ion batteries

TL;DR: In this article, the mechanisms of lithium-ion battery ageing are reviewed and evaluated, and the most promising candidate as the power source for (hybrid) electric vehicles and stationary energy storage.
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Nickel-Rich Layered Cathode Materials for Automotive Lithium-Ion Batteries: Achievements and Perspectives

TL;DR: In this paper, the potential and limitations of nickel-rich cathode materials are compared with reference to realistic target values from the automotive industry, and how future automotive targets can be achieved through fine control of the structural and microstructural properties.
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Issue and challenges facing rechargeable thin film lithium batteries

TL;DR: In this paper, a review of the development of lithium-based thin-film rechargeable batteries highlight ongoing research strategies and discuss the challenges that remain regarding the discovery of nanomaterials as electrolytes and electrodes for lithium batteries also describes the possible evolution of lithium technology and evaluates the expected improvements, arising from new materials to cell technology.
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Review—Li-Rich Layered Oxide Cathodes for Next-Generation Li-Ion Batteries: Chances and Challenges

TL;DR: In this article, the benefits of going back to fundamentals to rationalize and understand the new science at work with these Li-rich NMC phases are stressed and illustrated by the discovery of a new reversible anionic redox process.
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Synthesis, Structure, and Electrochemical Properties of the Layered Sodium Insertion Cathode Material: NaNi1/3Mn1/3Co1/3O2

TL;DR: In this article, a layered phase, NaNi1/3Mn 1/3Co1/ 3O2 (NaNMC), isostructural to NaCoO2 has been synthesized, leading to a capacity of 120 mAh·g−1 in the voltage range of 2.75 V and indicating its possible application in Na-ion batteries.
References
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Journal ArticleDOI

Electrochemistry and Structural Chemistry of LiNiO2 (R3̅m) for 4 Volt Secondary Lithium Cells

TL;DR: LiNiO[sub 2] was used for a 4 V secondary lithium cell in this paper, which exhibited more than 150 mAh/g of rechargeable capacity in the voltage range between 2.5 and 4.2 V in 1M LiClO(sub 4] propylene carbonate solution.
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Structure and electrochemistry of Li1±yNiO2 and a new Li2NiO2 phase with the Ni (OH)2 structure

TL;DR: In this paper, Li can be reversibly intercalated in Li 1- y NiO 2 for 0 ≤ y ≤ 0.6 and over this range of y the lattice constants of the 3R phase change reversibly.
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In situ x-ray diffraction and electrochemical studies of Li1−xNiO2

TL;DR: In this article, the structure of Li1−xNiO2 is studied as Li is electrochemically deintercalated from LiNiO 2 with in situ X-ray diffraction methods.
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Rechargeable LiNiO2 / Carbon Cells

TL;DR: In this article, the authors discuss the factors that play a role in the selection of appropriate lithium intercalation compounds for rechargeable cells, and show that LiNiO{sub 2}/coke cells have high energy density, long cycle life, excellent high-temperature performance, low self-discharge rates, can be repeatedly discharged to zero volts without damage, and are easily fabricated.
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The Rietveld Method

Fujio Izumi
TL;DR: The Rietveld method is described in this article, where structure and lattice parameters are directly refined from powder diffraction data and several functions such as extinction correction, preferred orientation, and profile shape function have been improved to give physical meanings to parameters contained in them.
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