Investigating the Crystallization Kinetics Via Time‐Resolved Neutron Diffraction

Author(s):  
Marco Zanatta ◽  
Caterina Petrillo ◽  
Francesco Sacchetti
1986 ◽  
Vol 40a ◽  
pp. 126-141 ◽  
Author(s):  
A. Nørlund Christensen ◽  
H. Fjellvåg ◽  
M. S. Lehmann ◽  
R. Zingales ◽  
Inger Vikholm ◽  
...  

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

2018 ◽  
Vol 51 (3) ◽  
pp. 630-634 ◽  
Author(s):  
Takuro Kawasaki ◽  
Yasuhiro Inamura ◽  
Takayoshi Ito ◽  
Takeshi Nakatani ◽  
Stefanus Harjo ◽  
...  

A time-resolved time-of-flight neutron diffraction technique to characterize the structural properties of materials during cyclic tests has been developed for the neutron diffractometers at J-PARC. Using this technique, diffracted neutrons and the applied cyclic conditions are recorded as event data together with time information. The amplitude and phase of the conditions of all recorded neutron signals can be specified by using the characteristics of the event data. By adopting the developed technique, the behaviors of the crystal lattice and domains of the piezoelectric material in a multilayer-type piezoelectric actuator driven by a cyclic electric field were evaluated. The developed technique enabled the collection and processing of diffraction data for all levels of the applied electric field, as opposed to only the highest and lowest levels. The variation in diffraction intensity during the application of a cyclic electric field was obtained successfully, and the hysteresis-like behaviors of both the lattice strain and the 90° domain switching were revealed.


1987 ◽  
Vol 56 (9) ◽  
pp. 3196-3200 ◽  
Author(s):  
Susumu Katano ◽  
Yukio Morii ◽  
Masashi Iizumi ◽  
H. R. Child ◽  
R. M. Nicklow

1986 ◽  
Vol 16 (6) ◽  
pp. 871-874 ◽  
Author(s):  
A.Nørlund Christensen ◽  
H. Fjellvåg ◽  
M.S. Lehmann

2004 ◽  
Vol 19 (10) ◽  
pp. 2938-2946 ◽  
Author(s):  
Chain-Ming Lee ◽  
Yeong-Iuan Lin ◽  
Tsung-Shune Chin

Isothermal crystallization kinetics of amorphous Ga–Sb–Te films was studied by means of a time-resolved optical transmission method. Thin films with compositions along the pseudo-binary tie-lines Sb7Te3–GaSb and Sb2Te3–GaSb in the ternary phase diagram were prepared by the co-sputtering method. Crystallization of GaSbTe films reveals a two-stage process: an initial surface nucleation and coarsening (Stage 1) followed by the one-dimensional grain growth (Stage 2). The kinetic exponent (n) value in Stage 1 shows strong dependence on film compositions, while that of Stage 2 is less dependent. The activation energy in Stage 1 increases with increasing GaSb content and reaches the maximum values at compositions close to GaSb, but a decreasing trend was observed in Stage 2. Kinetics parameters between isothermal crystallization of thin films and non-isothermal crystallization of powder samples analyzed by differential scanning colorimetry [J. Mater. Res. 19, 2929 (2004)] are compared. The kinetic parameters in Stage 1 show much correspondence with those of non-isothermal cases in comparable kinetic exponents but with lower activation energies. The discrepancies between nonisothermal and isothermal kinetics are attributed to the sample morphology and the constraint effects.


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.


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