scholarly journals Magnetism and ion diffusion in honeycomb layered oxide $${\hbox {K}_2\hbox {Ni}_2\hbox {TeO}_6}$$

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Nami Matsubara ◽  
Elisabetta Nocerino ◽  
Ola Kenji Forslund ◽  
Anton Zubayer ◽  
Konstantinos Papadopoulos ◽  
...  

Abstract In the quest for developing novel and efficient batteries, a great interest has been raised for sustainable K-based honeycomb layer oxide materials, both for their application in energy devices as well as for their fundamental material properties. A key issue in the realization of efficient batteries based on such compounds, is to understand the K-ion diffusion mechanism. However, investigation of potassium-ion (K$$^+$$ + ) dynamics in materials using e.g. NMR and related techniques has so far been very challenging, due to its inherently weak nuclear magnetic moment, in contrast to other alkali ions such as lithium and sodium. Spin-polarised muons, having a high gyromagnetic ratio, make the muon spin rotation and relaxation ($$\mu ^+$$ μ + SR) technique ideal for probing ions dynamics in these types of energy materials. Here we present a study of the low-temperature magnetic properties as well as K$$^+$$ + dynamics in honeycomb layered oxide material $${\hbox {K}_2\hbox {Ni}_2\hbox {TeO}_6}$$ K 2 Ni 2 TeO 6  using mainly the $$\mu ^+$$ μ + SR technique. Our low-temperature $$\mu ^+$$ μ + SR results together with complementary magnetic susceptibility measurements find an antiferromagnetic transition at $$T_{\mathrm{N}}\approx 27$$ T N ≈ 27  K. Further $${\mu}^{+}$$ μ + SR studies performed at higher temperatures reveal that potassium ions (K$$^+$$ + ) become mobile above 200 K and the activation energy for the diffusion process is obtained as $$E_{\mathrm{a}}=121 (13)$$ E a = 121 ( 13 )  meV. This is the first time that K$$^+$$ + dynamics in potassium-based battery materials has been measured using $$\mu ^+$$ μ + SR. Assisted by high-resolution neutron diffraction, the temperature dependence of the K-ion self diffusion constant is also extracted. Finally our results also reveal that K-ion diffusion occurs predominantly at the surface of the powder particles. This opens future possibilities for potentially improving ion diffusion as well as K-ion battery device performance using nano-structuring and surface coatings of the particles.

2014 ◽  
Vol 70 (a1) ◽  
pp. C363-C363
Author(s):  
Marisa Medarde ◽  
Mattia Mena ◽  
Jorge Gavilano ◽  
Ekaterina Pomjakushina ◽  
Jun Sugiyama ◽  
...  

One of the most important scientific problems faced by our society is how to convert and store clean energy. In order to achieve a significant progress in this field we need to understand the fundamental dynamical processes that govern the transfer of energy on an atomic scale. For many energy devices such as solid-state batteries and solid-oxide fuel cells, this means understanding and controlling the complex mechanisms of ion diffusion in solid matter. Because of the unusual evolution of correlated electronic properties (frustrated magnetism and superconductivity), the layered Co-oxide family NaxCoO2 (0<x<1), object of this work, has been extensively studied during the last decade. More recently it has also attracted the attention of applied sciences, mainly because of its structural similarity with LixCoO2, one of the most common Li-ion battery electrodes. In view of the larger abundance of Na in the earth crust with respect to Li, Na-ion batteries enjoy an increased attention. Hence we decided to investigate the Na-ion diffusion in this material, whose possible use as cathode for solid-state rechargeable batteries has recently been proposed [1]. The present study reports the observation of a crossover from quasi-1D to 2D Na-ion diffusion in Na0.7CoO2. High resolution neutron powder diffraction data indicate the existence of two structural transitions at T1=290K and T2=400K [2]. We present here evidence indicating that both transitions are closely related to changes in the Na-ion mobility. Analysis of the anomalies in the Na-Na distances, the Debye-Waller factors and the scattering density in the paths connecting neighbouring Na sites strongly suggest that Na-ion diffusion starts at T1, although for T1<T<T2 it occurs preferentially along quasi-1D paths. A fully isotropic diffusion is only observed for T>T2, coinciding with the equalization of all first-neighbor Na-Na distances in the structure [2]. These findings provide new insight on the subtle mechanisms controlling the Na-ion diffusion in the NaxCoO2 family and could be used for the design of related energy materials with improved functional properties. Fig. 1. Fourier difference maps of the z = 0.25 Na planes at T = 50, 320 and 450 K showing the evolution of the residual scattering density in the paths connecting the Na1 and Na2 sites (from ref.[2]).


Author(s):  
Siyuan Wu ◽  
Ruijuan Xiao ◽  
Hong Li ◽  
Liquan Chen

Understanding the ion diffusion mechanism is one of the key preconditions for designing superionic conductors in solid state lithium batteries and many other energy devices. Besides single-cation vacancy/interstitial-assisted and multi-cation...


2013 ◽  
Vol 3 (1) ◽  
Author(s):  
L. J. Chang ◽  
M. R. Lees ◽  
G. Balakrishnan ◽  
Y.-J. Kao ◽  
A. D. Hillier

Author(s):  
Zhiqiang Niu ◽  
Valerie Pinfield ◽  
Billy Wu ◽  
Huizhi Wang ◽  
Kui Jiao ◽  
...  

Porous energy materials are essential components of many energy devices and systems, the development of which have been long plagued by two main challenges. The first is the ‘curse of...


1999 ◽  
Vol 59 (5) ◽  
pp. 3775-3782 ◽  
Author(s):  
Th. Jestädt ◽  
K. H. Chow ◽  
S. J. Blundell ◽  
W. Hayes ◽  
F. L. Pratt ◽  
...  

1991 ◽  
Vol 15 (5) ◽  
pp. 547-552 ◽  
Author(s):  
L. P Le ◽  
G. M Luke ◽  
B. J Sternlieb ◽  
W. D Wu ◽  
Y. J Uemura ◽  
...  

2012 ◽  
Vol 85 (9) ◽  
Author(s):  
Vyacheslav G. Storchak ◽  
Oleg E. Parfenov ◽  
Dmitry G. Eshchenko ◽  
Roger L. Lichti ◽  
Patrick W. Mengyan ◽  
...  

2006 ◽  
Vol 73 (22) ◽  
Author(s):  
J. Sugiyama ◽  
Y. Ikedo ◽  
K. Mukai ◽  
J. H. Brewer ◽  
E. J. Ansaldo ◽  
...  

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