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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

The electron attachment energy of the aqueous hydroxyl radical predicted from the detachment energy of the aqueous hydroxide anion
C Adriaanse, M Sulpizi, J VandeVondele, M Sprik
– Journal of the American Chemical Society
(2009)
131,
6046
Adsorption of a sodium ion on a smectite clay from constrained ab initio molecular dynamics simulations
JL Suter, ES Boek, M Sprik
– Journal of Physical Chemistry C
(2008)
112,
18832
Acidity constants from vertical energy gaps: Density functional theory based molecular dynamics implementation
M Sulpizi, M Sprik
– Physical chemistry chemical physics : PCCP
(2008)
10,
5238
First Principles Study of Alkali−Tyrosine Complexes: Alkali Solvation and Redox Properties
F Costanzo, M Sulpizi, R Guido Della Valle, M Sprik
– Journal of chemical theory and computation
(2008)
4,
1049
PHYS 168-Solvation and reactivity of the aqueous hydroxyl radical
C Adriaanse, M Sulpizi, J VandeVondele, M Sprik
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2008)
235,
COMP 62-Computation of acidity constants in solution from vertical energy gaps
M Sulpizi, A Shah, M Sprik
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2008)
235,
A classical point charge model study of system size dependence of oxidation and reorganization free energies in aqueous solution.
R Ayala, M Sprik
– The journal of physical chemistry. B
(2007)
112,
257
Redox free energies and one-electron energy levels in density functional theory based ab initio molecular dynamics
J VandeVondele, R Ayala, M Sulpizi, M Sprik
– Journal of Electroanalytical Chemistry
(2007)
607,
113
PHYS 97-Density functional based molecular dynamics simulation of the aqueous hydroxyl and thiyl radical
M Sprik, C Adriaanse, M Sulpizi, J VandeVondele
– ABSTR PAP AM CHEM S
(2007)
234,
PHYS 99-Water addition along with reduction of aqueous ruthenium complexes by ab initio free energy calculation method for bond breaking/formation coupled to electron transfer
Y Tateyama, J Blumberger, T Ohno, M Sprik
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2007)
234,
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Research Group

Research Interest Groups

Telephone number

01223 336376

Email address

ms284@cam.ac.uk