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Electrochemical potassium/lithium-ion intercalation into TiSe2: Kinetics and mechanism

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TLDR
In this paper, the potassiation/depotassiation reaction mechanism was unraveled based on the analysis of in-situ X-ray diffraction (XRD), XPS, and ex-Situ transmission electron microscope (TEM) results.
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This article is published in Energy Storage Materials.The article was published on 2019-01-01 and is currently open access. It has received 84 citations till now. The article focuses on the topics: Lithium & Reaction mechanism.

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Physical Review B

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Chemistry of materials

TL;DR: In this paper, the authors discuss the importance of structure and bonding in chemistry, and how the understanding of the chemical bond provides a basis to understand chemistry and to do new chemistry.
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Insertion Electrode Materials for Rechargeable Lithium Batteries

TL;DR: In this article, the performance and safety of rechargeable batteries depend strongly on the materials used and future trends, such as alternative materials for achieving higher specific charges are discussed, and a review of the insertion materials suitable for negative and positive insertion electrodes is presented.
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Solid State Ionics

TL;DR: The main feature of this area of science and emerging technology is the rapid transport of atomic or ionic species within solids, and various phenomena, of both scientific and technological interest, that are related to it as discussed by the authors.

Physical Review B

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Q1. What are the contributions mentioned in the paper "Electrochemical potassium/lithium-ion intercalation into tise2: kinetics and mechanism" ?

In this work, TiSe2was, for the first time, investigated as an intercalated-type electrode for potassium storage due to its large interlayer space. Meanwhile, the lithium storage behaviour and the relevant lithiation/delithiation reaction mechanism were also studied in detail. Authors Peng Li, Xiaobo Zheng, Haoxiang Yu, Guoqiang Zhao, Jie Shu, Xun Xu, Wenping Sun, and Shi Xue Dou This journal article is available at Research Online: https: //ro. uow.