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Yusuf Hamied Department of Chemistry

 

Physical chemistry of electrochemical interfaces

The interface between an electrode and electrolytic solution is a location of strong interaction between chemistry and physics. The adsorption/dissolution and oxidation/reduction of chemical species is controlled by the physics of excess charge accumulated at both sides of the interface. The theoretical and computational tools to investigate these two aspects tend however to be different. The chemistry normally requires the atomistic detail of realistic force fields or electronic structure calculation. The physics can be studied using more elementary particle models or continuum theory focusing instead on the thermodynamics and statistical mechanics of non-uniform systems. Here a consistent theoretical treatment is crucial. An example is the interaction between the electrostatic forces at charged interfaces and stress, both in the solution and solid electrode. This is the field of thermo-electromechanics, which recently has become the main subject of my research interests after a long period of working on atomistic modelling of electrochemical interfaces.

Publications

Diabatic free energy curves and coordination fluctuations for the aqueous Ag+ Ag2+ redox couple: A biased Born-Oppenheimer molecular dynamics investigation
J Blumberger, I Tavernelli, ML Klein, M Sprik
– Journal of Chemical Physics
(2006)
124,
064507
Redox Free Energies from Vertical Energy Gaps: Ab Initio Molecular Dynamics Implementation
J Blumberger, M Sprik
– Computer Simulations in Condensed Matter Systems: From Materials to Chemical Biology, Vol 2
(2006)
704,
481
Quantum versus classical electron transfer energy as reaction coordinate for the aqueous Ru2+/Ru3+ redox reaction
J Blumberger, M Sprik
– Theoretical Chemistry Accounts
(2005)
115,
113
Density Functional Theory Study of Tetrathiafulvalene and Thianthrene in Acetonitrile:  Structure, Dynamics, and Redox Properties
J VandeVondele, R Lynden-Bell, EJ Meijer, M Sprik
– The journal of physical chemistry. B
(2005)
110,
3614
Editorial: a tribute to Michele Parrinello: from physics via chemistry to biology.
W Andreoni, D Marx, M Sprik
– Chemphyschem : a European journal of chemical physics and physical chemistry
(2005)
6,
1671
On the position of the highest occupied molecular orbital in aqueous solutions of simple ions
P Hunt, M Sprik
– ChemPhysChem
(2005)
6,
1805
Infrared spectroscopy of N-methylacetamide revisited by ab initio molecular dynamics simulations
MP Gaigeot, R Vuilleumier, M Sprik, D Borgis
– Journal of Chemical Theory and Computation
(2005)
1,
772
Ab initio molecular dynamics simulation of redox reactions in solution
J Blumberger, Y Tateyama, M Sprik
– Computer Physics Communications
(2005)
169,
256
Toward a Monte Carlo program for simulating vapor-liquid phase equilibria from first principles
MJ McGrath, JI Siepmann, IFW Kuo, CJ Mundy, J VandeVondele, M Sprik, E Hutter, F Mohamed, M Krack, M Parrinello
– Computer Physics Communications
(2005)
169,
289
Density-functional molecular-dynamics study of the redox reactions of two anionic, aqueous transition-metal complexes
Y Tateyama, J Blumberger, M Sprik, I Tavernelli
– The Journal of Chemical Physics
(2005)
122,
234505
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Research Group

Research Interest Groups

Telephone number

01223 336376

Email address

ms284@cam.ac.uk