Catalytic activity to lithium-thionylchloride battery of different transitional metal carboxylporphyrins

Author:

Lü Xiangfei12,Hu Nan jiang3,Li Jun1,Zhang Zeng qi1,Tang Wei3

Affiliation:

1. Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, Shaanxi 710069, PR China

2. Department of Environmental Engineering, College of Resource and Environment Science, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China

3. Department of Process Equipment Control and Engineering, College of Light Industry and Energy, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China

Abstract

The 5-(4-carboxylatomethoxy)phenyl-10,15,20-triphenyl porphyrin ( H 2 Pp ) and its transition metal complex (MPp, M = Zn 2+, Co 2+, Ni 2+, Cu 2+) were synthesized and characterized by IR, UV-vis, MS and elementary analysis. Electrocatalytic effects associated with the reduction of thionyl chloride in a lithium/thionyl chloride ( Li / SOCl 2) battery containing H 2 Pp and its transition metal complex (MPp, M = Zn 2+, Co 2+, Ni 2+, Cu 2+) are evaluated by the relative energy of the battery and discharge time. The results indicate that the energy of Li / SOCl 2 battery catalyzed by CuPp and ZnPp is 103.7%, 106.3%, respectively, higher than that of Li / SOCl 2 battery in the absence of the porphyrins. The energy of Li / SOCl 2 battery whose electrolyte contains NiPp and CoPp is similar to that of the cell in the absence of these complexes. It shows that the electronic configuration of the central metal ion influences a charge-transfer process during the reduction of thionyl chloride. With the increasing numbers of d electrons of the central metal ion, the catalytic activity of MPps was enhanced. The ZnPp with electronic configuration d10 of central metal ion exhibits relatively high catalytic activity.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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