Back to results

Massachusetts Institute of Technology

Metal metaphosphate complexes for redox flow batteries

Abstract

dc:description.abstract

In this thesis, possibility of using anionic metal complexes to limit crossover of active species in redox flow batteries was explored. A series of first row transition metal trimetaphosphate complexes as bis(triphenylphosphine)iminium (PPN) salts have been prepared. Their electrochemical properties have been studied to evaluate them for redox flow battery applications. [PPN]₃[Fe(P₃Og)₂] and [PPN]₂[VO(P₃O₉)(acac)] were identified as a suitable couple for a dual-active-species redox flow battery with an open cell potential of 1.5 V. [PPN]₃[V(P₃Og)₂] can be oxidized and reduced within the stability window of acetonitrile and it is therefor a promising candidate for single-active-species redox flow battery applications. The difference in redox potentials between the V(III)/V(IV) and V(II)/V(III) couples is 2.7 V which is the highest peak to peak separation reported in the literature to date.

Degree

thesis:*
Department dc:contributor.department
Massachusetts Institute of Technology. Department of Chemistry.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2016

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Avena, Laura
Advisor dc:contributor.advisor
  • Christopher C. Cummins.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/107568
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/107568

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Avena, Laura. Metal metaphosphate complexes for redox flow batteries. Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/107568