Synthesis and performance evaluation of binuclear metal phthalocyanines as high-efficiency electrocatalysts for Li/SOCl 2 batteries

Abstract Two series of binuclear metal phthalocyanine complexes M 2 (PcTN) 2 Nap and M 2 (PcTA) 2 Nap (M = Mn 2+ , Fe 2+ , Co 2+ , Cu 2+ ) were designed and synthesized through the liquid solvent method and amination reaction. Elemental analysis, IR, and UV-vis spectroscopy were applied to character...

Full description

Saved in:
Bibliographic Details
Published inJournal of materials research Vol. 33; no. 16; pp. 2376 - 2384
Main Authors Su, Yuanyuan, Zhang, Ying, Zhang, Ronglan, Yang, Fei, Zhao, Jianshe
Format Journal Article
LanguageEnglish
Published 28.08.2018
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Two series of binuclear metal phthalocyanine complexes M 2 (PcTN) 2 Nap and M 2 (PcTA) 2 Nap (M = Mn 2+ , Fe 2+ , Co 2+ , Cu 2+ ) were designed and synthesized through the liquid solvent method and amination reaction. Elemental analysis, IR, and UV-vis spectroscopy were applied to characterize the compounds. To evaluate their catalytic performance, all the compounds were respectively added into the electrolyte of Li/SOCl 2 battery systems as well as three-electrode systems for cyclic voltammetry (CV) measurements. The research studies indicate that the average discharge voltage and discharge time of the battery could be effectively enhanced by 0.2440 V and 810.7 s when compared with the battery in the absence of the compounds. As for capacities of the batteries containing catalysts, they were also found to have an improvement of 51.78–91.62%. Among the effects of diverse metal ions on the catalytic performance of phthalocyanines, the complexes whose center metal ions were Mn 2+ or Co 2+ exhibited relatively high catalytic performance. Meanwhile, combined with experimental results of CV analyses, the suggested catalytic mechanism of binuclear phthalocyanines for catalyzing Li/SOCl 2 batteries had been proposed.
ISSN:0884-2914
2044-5326
DOI:10.1557/jmr.2018.238