Electrostatically Driven Multielectron Transfer for the Photocatalytic Regeneration of Nicotinamide Cofactor

ACS Catalysis ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 5522-5528 ◽  
Author(s):  
Soumendu Roy ◽  
Vanshika Jain ◽  
Radha Krishna Kashyap ◽  
Anish Rao ◽  
Pramod P. Pillai
2020 ◽  
Author(s):  
Marco Amores ◽  
Keisuke Wada ◽  
Ken Sakaushi ◽  
Hiroshi Nishihara

Coordination polymers represent a suitable model to study redox mechanisms in materials where both metal cation and ligand undergo electrochemical reactions and are capable to proceed through reversible multielectron-transfer processes with insertion of cation and anion into their open structures. Designing new coordination polymers for electrochemical energy storage with improved performance relays also on the understanding of their structure-properties relationship. Here, we present a family of copper-based coordination polymer with hexafunctionalized benzene ligands forming a kagome-type layered structure, where the in uence of the functional groups in their structure and electrochemical properties is investigated. Their chemical and structural properties have been explored by means of PXRD, and FTIR and Raman spectroscopies, followed by investigation of their electrochemical performance in Li half-cells by CV and galvanostatic cycling techniques. Ex-situ PXRD, Raman, XPS and ToF-SIMS measurements of cycled electrodes have been carried out providing insights into the redox mechanism of these copper-based coordination polymers as positive electrode materials.<br>


2020 ◽  
Vol 3 (5) ◽  
pp. 4377-4383
Author(s):  
Akihiro Ohira ◽  
Takashi Funaki ◽  
Erika Ishida ◽  
Je-Deok Kim ◽  
Yukari Sato

2010 ◽  
Vol 24 (24) ◽  
pp. 4811-4820
Author(s):  
Y. P. ZHANG ◽  
F. S. ZHANG ◽  
Y. GAO ◽  
H. W. CHANG ◽  
G. Q. XIAO

The process of multielectron transfer from a Na 4 cluster induced by highly charged C 6+, C 4+, C 2+ and C + ions is studied using the method of time-dependent density functional theory within the local density approximation combined with the use of pseudopotential. The evolution of dipole moment changes and emitted electrons in Na 4 is obtained and the time-dependent probabilities with various charges are deduced. It is shown that the Na 4 cluster is strongly ionized by C 6+ and that the number of emitted electrons per atom of Na 4 is larger than that of Na 2 under the same condition. One can find that the detailed information of the emitted electrons from Na 4 is different from the same from Na 2, which is possibly related to the difference in structure between the two clusters.


1999 ◽  
Vol 38 (11) ◽  
pp. 2705-2708 ◽  
Author(s):  
Laura A. Worl ◽  
Wayne E. Jones ◽  
Geoffrey F. Strouse ◽  
Janet N. Younathan ◽  
Earl Danielson ◽  
...  

2019 ◽  
Vol 380 ◽  
pp. 186-194
Author(s):  
Yevheniia Markushyna ◽  
Antje Völkel ◽  
Aleksandr Savateev ◽  
Markus Antonietti ◽  
Svitlana Filonenko

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