Emerging N-Type Redox-Active Radical Polymer for a Totally Organic Polymer-Based Rechargeable Battery

2009 ◽  
Vol 21 (16) ◽  
pp. 1627-1630 ◽  
Author(s):  
Takeo Suga ◽  
Hiroki Ohshiro ◽  
Shuhei Sugita ◽  
Kenichi Oyaizu ◽  
Hiroyuki Nishide
Energies ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2480
Author(s):  
Evgenii V. Beletskii ◽  
Daniil A. Lukyanov ◽  
Petr S. Vlasov ◽  
Andrei N. Yankin ◽  
Arslan B. Atangulov ◽  
...  

Conjugated coordination polymers attract attention as materials for electrochemical energy storage, mostly as cathode materials for supercapacitors. Faradaic capacity may be introduced to such materials using redox-active building blocks, metals, or ligands. Using this strategy, a novel hybrid cathode material was developed based on a Ni2+ metal-organic polymer. The proposed material, in addition to double-layer capacitance, shows high pseudocapacitance, which arises from the contributions of both the metal center and ligand. A tailoring strategy in the ligand design allows us to minimize the molecular weight of the ligand, which increases its gravimetric energy. According to computational results, the ligand makes the prevailing contribution to the pseudocapacitance of the material. Different approaches to metal–organic polymer (MOP) synthesis were implemented, and the obtained materials were examined by FTIR, Raman spectroscopy, powder XRD, SEM/EDX (energy-dispersive X-ray spectroscopy), TEM, and thermal analysis. Energy-storage performance was comparatively studied with cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD). As a result, materials with an excellent discharge capacity were obtained, reaching the gravimetric energy density of common inorganic cathode materials.


2013 ◽  
Vol 49 (6) ◽  
pp. 567-569 ◽  
Author(s):  
L. M. Zhu ◽  
A. W. Lei ◽  
Y. L. Cao ◽  
X. P. Ai ◽  
H. X. Yang

2018 ◽  
Vol 54 (50) ◽  
pp. 6796-6799 ◽  
Author(s):  
Sujoy Bandyopadhyay ◽  
Chanderpratap Singh ◽  
Priyajit Jash ◽  
MD. Waseem Hussain ◽  
Amit Paul ◽  
...  

A pristine porous organic polymer with a polyaromatic core of pyrene and redox-active functionalities exhibits remarkable supercapacitor performance with long-term cyclic stability.


RSC Advances ◽  
2015 ◽  
Vol 5 (29) ◽  
pp. 22947-22950 ◽  
Author(s):  
Ali A. Golriz ◽  
Takeo Suga ◽  
Hiroyuki Nishide ◽  
Rüdiger Berger ◽  
Jochen S. Gutmann

Redox-active, phenothiazine-functionalized polymers were synthesized and employed as a promising cathode-active material (∼3.7 V vs. Li, 77 Ah kg−1) in a rechargeable battery.


2010 ◽  
Vol 23 (6) ◽  
pp. 751-754 ◽  
Author(s):  
Takeo Suga ◽  
Shuhei Sugita ◽  
Hiroki Ohshiro ◽  
Kenichi Oyaizu ◽  
Hiroyuki Nishide

2018 ◽  
Vol 6 (40) ◽  
pp. 19834-19842 ◽  
Author(s):  
Sajad Ahmad Bhat ◽  
Chayanika Das ◽  
Tapas Kumar Maji

Metallated redox active porous organic polymer for water oxidation.


2019 ◽  
Vol 64 (1) ◽  
pp. 45-53 ◽  
Author(s):  
Elias S.J. Arnér

Abstract Selenocysteine (Sec), the sulfur-to-selenium substituted variant of cysteine (Cys), is the defining entity of selenoproteins. These are naturally expressed in many diverse organisms and constitute a unique class of proteins. As a result of the physicochemical characteristics of selenium when compared with sulfur, Sec is typically more reactive than Cys while participating in similar reactions, and there are also some qualitative differences in the reactivities between the two amino acids. This minireview discusses the types of modifications of Sec in selenoproteins that have thus far been experimentally validated. These modifications include direct covalent binding through the Se atom of Sec to other chalcogen atoms (S, O and Se) as present in redox active molecular motifs, derivatization of Sec via the direct covalent binding to non-chalcogen elements (Ni, Mb, N, Au and C), and the loss of Se from Sec resulting in formation of dehydroalanine. To understand the nature of these Sec modifications is crucial for an understanding of selenoprotein reactivities in biological, physiological and pathophysiological contexts.


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