scholarly journals Identifying signatures of thermal and non-thermal reaction pathways in plasmon induced H2 + D2 exchange reaction

Author(s):  
Amaraja Taur ◽  
Saurabh Kumar Singh ◽  
Pranav Ravindra Shirhatti

In this work we demonstrate a strategy for identifying experimental signatures of thermal and non-thermal effects in plasmon mediated heterogeneous catalytic chemistry, a topic widely debated and discussed in the literature. Our method is based on monitoring the progress of plasmon-induced (or thermally-driven) reaction, carried out in a closed system, all the way to equilibrium. Initial part of evolution of the reaction provides information about kinetics, whereas at later times the equilibrium concentrations provide information about effective temperature at the reaction sites. Combining these two pieces of information we estimate the activation energies. Using this strategy on H 2 (g) + D 2 (g) <-->2 HD(g) isotope exchange reaction, catalyzed by Au nanoparticles under thermally-driven and light-induced conditions, we estimate the activation energies to be 0.75 ± 0.02 eV and 0.21 ± 0.02 eV, respectively. These vastly different activation energies observed are interpreted as a signature of different reaction pathways followed by the system under thermally-driven and light-induced conditions.

2021 ◽  
Author(s):  
Amaraja Taur ◽  
Saurabh Kumar Singh ◽  
Pranav Ravindra Shirhatti

In this work we demonstrate a strategy for identifying experimental signatures of thermal and non-thermal effects in plasmon mediated heterogeneous catalytic chemistry, a topic widely debated and discussed in the literature. Our method is based on monitoring the progress of plasmon induced (or thermally driven) reaction, carried out in a closed system, all the way to equilibrium. Initial part of evolution of the reaction provides information about kinetics, where as at later times the equilibrium concentrations provide information about effective temperature at the reaction sites. Combining these two pieces of information we estimate the activation energies. Using this strategy on H2 (g) + D2 (g) <--> 2 HD(g) isotope exchange reaction, catalyzed by Au nanoparticles under thermally driven and light induced conditions, we estimate the activation energies to be 0.75 ± 0.02 and 0.21 ± 0.02, respectively. These vastly different activation energies observed are interpreted as signatures of different reaction pathways followed by the system under thermally driven and light induced conditions.


Author(s):  
Lars Mohrhusen ◽  
Katharina Al-Shamery

Tungsten oxide clusters deposited on rutile TiO2 (110) single crystals were used as a model system for heterogenous oxide-oxide bifunctional catalysts. The population of different thermal reaction routes in methanol...


1997 ◽  
Vol 250 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Atsushi Baba ◽  
Masabumi Nishikawa ◽  
Takanori Eguchi

1989 ◽  
Vol 67 (5) ◽  
pp. 857-861 ◽  
Author(s):  
Shin-Ichi Miyamoto ◽  
Tetsuo Sakka ◽  
Matae Iwasaki

The reaction rate of hydrogen isotope exchange between D2 and H2O catalyzed by platinum plate is studied. The exchange reaction is described with the kinetic model which is the modification of that for the exchange reaction catalyzed by alumina-supported platinum catalyst. For the comparison of experimental results with this model relative amount of the number of sites for hydrogen adsorption was estimated from the initial rate of hydrogen isotope exchange between H2 and D2 on the same surface. The results show that the kinetic model is applicable for the plate catalyst if the number of the sites for hydrogen absorption, which is very sensitive to the surface state of the catalyst, was estimated not from the macroscopic surface area but from our scheme. Keywords: hydrogen isotope exchange reaction, platinum plate as catalyst.


1983 ◽  
Vol 38 (10) ◽  
pp. 1072-1077
Author(s):  
Junji Fukuda ◽  
Yasuhiko Fujii ◽  
Makoto Okamoto

Abstract Displacement chromatography of electron-exchange reaction between U(IV) and U(VI) has been accomplished in an anion exchange resin column using Ti(III) ion as a reductant and Fe(III) ion as an oxidant. The details of the so-called redox-process for uranium isotope separation are described. The temperature dependencies of the elementary separation coefficient and the equilibrium constant of the isotope exchange reaction are discussed using the analytical data obtained by a series of separation experiments at different temperatures.


2014 ◽  
Vol 141 (6) ◽  
pp. 064311 ◽  
Author(s):  
Annalise L. Van Wyngarden ◽  
Kathleen A. Mar ◽  
Jim Quach ◽  
Anh P. Q. Nguyen ◽  
Aaron A. Wiegel ◽  
...  

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