Novel apparatus for the in situ study of hydrothermal crystallizations using time-resolved neutron diffraction

1999 ◽  
Vol 70 (8) ◽  
pp. 3391-3396 ◽  
Author(s):  
Richard I. Walton ◽  
Robin J. Francis ◽  
P. Shiv Halasyamani ◽  
Dermot O’ Hare ◽  
Ronald I. Smith ◽  
...  
2002 ◽  
Vol 122 ◽  
pp. 331-341 ◽  
Author(s):  
Richard I. Walton ◽  
Alexander Norquist ◽  
Ronald I. Smith ◽  
Dermot O'Hare

2020 ◽  
Vol 32 (20) ◽  
pp. 8993-9000
Author(s):  
Laura Paradis-Fortin ◽  
Pierric Lemoine ◽  
Carmelo Prestipino ◽  
Ventrapati Pavan Kumar ◽  
Bernard Raveau ◽  
...  

2002 ◽  
Vol 14 (2) ◽  
pp. 931-939 ◽  
Author(s):  
David Grosso ◽  
Florence Babonneau ◽  
Pierre-Antoine Albouy ◽  
Heinz Amenitsch ◽  
A. R. Balkenende ◽  
...  

2014 ◽  
Vol 136 (2) ◽  
pp. 630-633 ◽  
Author(s):  
Stefan J. Sedlmaier ◽  
Simon J. Cassidy ◽  
Richard G. Morris ◽  
Michael Drakopoulos ◽  
Christina Reinhard ◽  
...  

2014 ◽  
Vol 70 (a1) ◽  
pp. C353-C353 ◽  
Author(s):  
Neeraj Sharma

Lithium-ion batteries are ubiquitous in society, used in everything from children's toys to mobile electronic devices, providing portable power solutions. There is a continuous drive for the improvement of these batteries to meet the demands of higher power devices and uses. A large proportion of the function of lithium-ion batteries arises from the electrodes, and these are in turn mediated by the atomic-scale perturbations or changes in the crystal structure during an electrochemical process (e.g. battery use). Therefore, a method to both understand battery function and propose ideas to improve their performance is to probe the electrode crystal structure evolution in situ while an electrochemical process is occurring inside a battery. Our work has utilized the benefits of in situ neutron diffraction (e.g. sensitivity towards lithium) to literally track the time-resolved evolution of lithium in electrode materials used in lithium-ion batteries (see Figure 1). With this knowledge we have been able to directly relate electrochemical properties such as capacity and differences in charge/discharge behaviour of a battery to the content and distribution of lithium in the electrode crystal structure. This talk will showcase some of our in situ investigations of materials in lithium-ion batteries, such as LiCoO2, LiFePO4, Li1+yMn2O4, LiNi0.5Mn1.5O4 and Li4Ti5O12/TiO2 electrodes. In addition, selected examples of our work using time-resolved in situ X-ray diffraction to probe other batteries types, such as primary lithium and secondary (rechargeable) sodium-ion batteries will be presented. Using time-resolved diffraction data, a comprehensive atomic-scale picture of battery functionality can be modelled and permutations can be made to the electrodes and electrochemical conditions to optimize battery performance. Therefore, crystallography and electrochemistry can mesh together to solve our energy needs.


2020 ◽  
Author(s):  
Machteld Kamminga ◽  
Simon J. Cassidy ◽  
Partha P. Jana ◽  
Nicola D. Kelly ◽  
Simon J. Clarke

<div>Intercalation of lithium and ammonia into the layered semiconductor Bi2Se3 proceeds via a</div><div>hyperextended (by > 60 %) ammonia-rich intercalate, to eventually produce a layered compound</div><div>with lithium amide intercalated between the bismuth selenide layers which offer scope for further</div><div>chemical manipulation.</div>


2000 ◽  
Vol 71 (11) ◽  
pp. 4177 ◽  
Author(s):  
Margret J. Geselbracht ◽  
Richard I. Walton ◽  
E. Sarah Cowell ◽  
Franck Millange ◽  
Dermot O’Hare

2006 ◽  
Vol 128 (40) ◽  
pp. 13161-13174 ◽  
Author(s):  
Ronan Le Toquin ◽  
Werner Paulus ◽  
Alain Cousson ◽  
Carmelo Prestipino ◽  
Carlo Lamberti

2001 ◽  
Vol 123 (51) ◽  
pp. 12826-12831 ◽  
Author(s):  
Yuval Halpern ◽  
Vu Thieu ◽  
Robert W. Henning ◽  
Xiaoping Wang ◽  
Arthur J. Schultz

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