Tom Oliver McDonald

Dr. Tom Oliver McDonald

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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 September 2012 in Biomaterials Science
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Journal Article
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MZMischa Zelzer
Mischa Zelzer
STSimon J. Todd
Simon J. Todd
AHAndrew R. Hirst
Andrew R. Hirst
Tom Oliver McDonaldTom Oliver McDonald
Tom Oliver McDonald
RURein Ulijn
Rein Ulijn
Enzyme responsive materials (ERMs) are a class of stimuli responsive materials with broad application potential in biological settings. This review highlights current and potential future design strategies for ERMs and provides an overview of the present state of the art in the area.

14 September 2015 in Nature Chemistry
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Journal Article
Closed access
EDEmily R. Draper
Emily R. Draper
EEEdward G. B. Eden
Edward G. B. Eden
Tom Oliver McDonaldTom Oliver McDonald
Tom Oliver McDonald
DADave J. Adams
Dave J. Adams

24 September 2014 in Nanoscale
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Journal Article
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CCCatherine Colquhoun
Catherine Colquhoun
EDEmily R. Draper
Emily R. Draper
EEEdward G. B. Eden
Edward G. B. Eden
BCBeatrice N. Cattoz
Beatrice N. Cattoz
KMKyle L. Morris
Kyle L. Morris
Dave AdamsDave Adams
Dave Adams
Self-sorting in low molecular weight hydrogels can be used to prepare gels with different types of mechanical properties.

28 May 2014 in Journal of Materials Chemistry C
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EDEmily R. Draper
Emily R. Draper
JWJames J. Walsh
James J. Walsh
Tom Oliver McDonaldTom Oliver McDonald
Tom Oliver McDonald
MZMartijn A. Zwijnenburg
Martijn A. Zwijnenburg
PCPetra J. Cameron
Petra J. Cameron
Dave AdamsDave Adams
Dave Adams
The photoconductivity of perylene-bisimide gelators correlates with the perylene radical anion, which is unusually highly stable in air for many hours.

5 April 2013 in RSC Advances
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LCLin Chen
Lin Chen
Tom Oliver McDonaldTom Oliver McDonald
Tom Oliver McDonald
Dave AdamsDave Adams
Dave Adams
A range of functionalised-dipeptides are shown here to form gels on addition of Ca2+ to solutions at high pH. We show that the ability to form gels correlates with the hydrophobicity of the dipeptides, which determines whether worm-like micelles are formed at high pH. The dipeptides can be functionalised with a number of different groups including naphthalene rings as well as alkyl chains. The effect of aging on stock solutions and gels is discussed. We show that gels can also be formed when trivalent or polyvalent salts are added.

1 January 2018 in Journal of Materials Chemistry A
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Journal Article
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RWRobert Woodward
Robert Woodward
FMFoivos Markoulidis
Foivos Markoulidis
FLFrançois De Luca
François De Luca
DADavid B. Anthony
David B. Anthony
DMDaniel Malko
Daniel Malko
ABAlexander Bismarck
Alexander Bismarck
Amphiphilic reduced graphene oxide (rGO) is an efficient emulsifier for water-in-divinylbenzene (DVB) high internal phase emulsions. The polymerisation of the continuous DVB phase of the emulsion template and removal of water results in macroporous poly(divinylbenzene) (polyDVB). Subsequent pyrolysis of the poly(DVB) macroporous polymers yields ‘all-carbon’ foams containing micropores alongside emulsion templated-macropores, resulting in hierarchical porosity. The synthesis of carbon foams, or ‘carboHIPEs’, from poly(DVB) produced by polymerisation of rGO stabilised HIPEs provides both exceptionally high surface areas (up to 1820 m2 g−1) and excellent electrical conductivities (up to 285 S m−1), competing with the highest figures reported for carboHIPEs. The use of a 2D carbon emulsifier results in the elimination of post-carbonisation treatments to remove standard inorganic particulate emulsifiers, such as silica particles. It is demonstrated that rGO containing carboHIPEs are good candidates for supercapacitor electrodes where carboHIPEs derived from more conventional polymerised silica-stabilised HIPEs perform poorly. Supercapacitor devices featured a room-temperature ionic liquid electrolyte and electrodes derived from either rGO- or silica-containing poly(DVB)HIPEs demonstrated a maximum specific capacitance of 26 F g−1, an energy density of 5.2 W h kg−1 and a power density of 280 W kg−1.