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

Density functional molecular dynamics calculation of the dissociation constant of liquid water
M Sulpizi, M Sprik
ABSTR PAP AM CHEM S
(2009)
238
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
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
Acidity constants from vertical energy gaps: Density functional theory based molecular dynamics implementation
M Sulpizi, M Sprik
Phys Chem Chem Phys
(2008)
10
First principles study of alkali-tyrosine complexes: Alkali solvation and redox properties
F Costanzo, M Sulpizi, R Guido Della Valle, M Sprik
J Chem Theory Comput
(2008)
4
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
Journal of Physical Chemistry B
(2007)
112
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
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
ABSTR PAP AM CHEM S
(2007)
234

Research Group

Research Interest Groups

Telephone number

01223 336376

Email address

College