Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.631015
Title: Investigations of electron-coupled-proton-buffers : from fundamentals to application
Author: Rausch, Benjamin
ISNI:       0000 0004 5354 954X
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2014
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
The work detailed in this thesis is presented and discussed in six chapters, which constitute a general and progressive study into both inorganic and organic electron-coupled-proton buffers (ECPBs). ECPBs allow the decoupling of the oxygen evolving reaction and the hydrogen evolving reaction during electrolytic water splitting into two separated steps. A range of commercial and literature based inorganic polyoxometallates (POMs) were investigated to determine their redox potentials and solubility in aqueous media. Of these, the Keggin-structured POM silicotungstic acid (H4[SiW12O40], STA) was investigated in detail. The cyclic voltammogram (CV) of STA shows two reversible 1-electron redox waves on carbon electrodes at E1/2 = +0.01 V vs. NHE and E1/2 = –0.22 V vs. NHE, where the latter is cathodic of the reduction potential of hydrogen on platinum electrodes (E1/2 = ±0.00 V vs. NHE). Electrochemical studies, in combination with gas chromatography show that H4[SiW12O40] can be reduced by two electrons to form H6[SiW12O40] on carbon electrodes, while effectively suppressing hydrogen evolution during electrolysis. The reduced H6[SiW12O40] species can then be utilised for rapid and spontaneous hydrogen evolution, either on demand or via a continuous flow setup, if in contact with suitable catalysts. Platinum was found to be the best catalyst for spontaneous hydrogen evolution and was tested at a range of loadings, supported on carbon and ultimately indicated that an STA-based electrolytic system can utilise platinum up to 30 times more efficiently than a conventional proton-exchange-membrane electrolyser (PEME). A modified PEME was built for H4[SiW12O40] reduction and various methods for catalyst immobilisation were tested. In an attempt to mimic photosynthetic water splitting, a range of quinone derivatives were also investigated as organic, low molecular weight ECPBs. 1,4-hydroquinone-sulfonic acid was found to efficiently decouple hydrogen and oxygen evolution, with a redox potential of E1/2 = 0.65 V vs. NHE and showed an 80% – 90% energy efficiency compared to conventional electrolysis, whilst using 50% less catalytic platinum in the 2-step electrolysis.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.631015  DOI: Not available
Keywords: QD Chemistry
Share: