In Situ Time-Resolved XAFS Studies of Metal Particle Formation by Photoreduction in Polymer Solutions

Langmuir ◽  
2009 ◽  
Vol 25 (11) ◽  
pp. 6049-6061 ◽  
Author(s):  
Masafumi Harada ◽  
Yasuhiro Inada
Langmuir ◽  
2008 ◽  
Vol 24 (10) ◽  
pp. 5225-5228 ◽  
Author(s):  
P. Riello ◽  
M. Mattiazzi ◽  
J. S. Pedersen ◽  
A. Benedetti

Langmuir ◽  
2007 ◽  
Vol 23 (12) ◽  
pp. 6536-6543 ◽  
Author(s):  
Masafumi Harada ◽  
Hisahiro Einaga

Nanoscale ◽  
2010 ◽  
Vol 2 (11) ◽  
pp. 2447 ◽  
Author(s):  
Gaetano Campi ◽  
Alessandra Mari ◽  
Heinz Amenitsch ◽  
Augusto Pifferi ◽  
Carla Cannas ◽  
...  

2018 ◽  
Vol 123 (1) ◽  
pp. 817-824 ◽  
Author(s):  
Morihisa Saeki ◽  
Daiju Matsumura ◽  
Takumi Yomogida ◽  
Tomitsugu Taguchi ◽  
Takuya Tsuji ◽  
...  

Author(s):  
J. Allègre ◽  
P. Lefebvre ◽  
J. Camassel ◽  
B. Beaumont ◽  
Pierre Gibart

Time-resolved photoluminescence spectra have been recorded on three GaN epitaxial layers of thickness 2.5 μm, 7 μm and 16 μm, at various temperatures ranging from 8K to 300K. The layers were deposited by MOVPE on (0001) sapphire substrates with standard AlN buffer layers. To achieve good homogeneities, the growth was in-situ monitored by laser reflectometry. All GaN layers showed sharp excitonic peaks in cw PL and three excitonic contributions were seen by reflectivity. The recombination dynamics of excitons depends strongly upon the layer thickness. For the thinnest layer, exponential decays with τ ~ 35 ps have been measured for both XA and XB free excitons. For the thickest layer, the decay becomes biexponential with τ1 ~ 80 ps and τ2 ~ 250 ps. These values are preserved up to room temperature. By solving coupled rate equations in a four-level model, this evolution is interpreted in terms of the reduction of density of both shallow impurities and deep traps, versus layer thickness, roughly following a L−1 law.


2020 ◽  
Author(s):  
Luzia S. Germann ◽  
Sebastian T. Emmerling ◽  
Manuel Wilke ◽  
Robert E. Dinnebier ◽  
Mariarosa Moneghini ◽  
...  

Time-resolved mechanochemical cocrystallisation studies have so-far focused solely on neat and liquid-assisted grinding. Here, we report the monitoring of polymer-assisted grinding reactions using <i>in situ</i> X-ray powder diffraction, revealing that reaction rate is almost double compared to neat grinding and independent of the molecular weight and amount of used polymer additives.<br>


2019 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Matthew Tirrell

We have directly observed the <i>in situ</i> self-assembly kinetics of polyelectrolyte complex (PEC) micelles by synchrotron time-resolved small-angle X-ray scattering, equipped with a stopped-flow device that provides millisecond temporal resolution. This work has elucidated one general kinetic pathway for the process of PEC micelle formation, which provides useful physical insights for increasing our fundamental understanding of complexation and self-assembly dynamics driven by electrostatic interactions that occur on ultrafast timescales.


Sign in / Sign up

Export Citation Format

Share Document