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Yusuf Hamied Department of Chemistry

 

Professor of Theoretical Chemistry

What we do...

Our theoretical research group uses mathematical and computational techniques to investigate quantum behaviour in the motion of atomic nuclei. We carry out computer simulations which illustrate how quantum mechanics changes the motion of atoms and molecules in chemical reactions and inside liquid water and ice.

Research

Our research investigates how the quantum properties of atomic nuclei affect chemical reaction rates and mechanisms. We develop and apply a wide range of theories and computational techniques, from exact solutions of the Schrödinger equation for small systems, to approximate Feynman path- integral approaches for larger systems.

First-principles calculations of wave functions of chemical reactions

We were the first group to calculate a complete time-dependent wave function that visualizes the entire dynamics of a chemical reaction from approach of the reactants through to scattering of the products into space. This work is done in collaboration with a leading experimental group (R.N. Zare, Stanford) who measure detailed product-scattering patterns that our calculations reproduce and interpret in terms of first-principles quantum mechanics.

Instanton simulations of quantum tunnelling

Instantons arise when Feynman path-integral theory is used to describe quantum tunnelling through barriers; they describe the dominant tunnelling path, which gives an approximate but physically rigorous description of the tunnelling dynamics. We have recently developed and extended instanton theory such that the instantons are represented by a series of beads which can be rapidly strung together to describe quantum tunnelling in complex systems. We are currently applying this method to tunnelling in water clusters (in collaboration with Prof. D.J. Wales), and to proton transfer reactions in solution.

Winding effects at conical intersections

Conical intersections arise when potential energy surfaces intersect. We have found that the nuclear wave functions at such intersections can be unwound, such that contributions from Feynman paths that wind different numbers of times around the intersection can be rigorously separated. This gives rise to quantum interference effects; we are currently investigating how such effects influence the efficiency of relaxation through a conical intersection.

Watch Professor Althorpe discuss his research

Publications

Instanton calculations of tunneling splittings for water dimer and trimer
JO Richardson, SC Althorpe, DJ Wales
– The Journal of chemical physics
(2011)
135,
124109
On the equivalence of two commonly used forms of semiclassical instanton theory.
SC Althorpe
– The Journal of chemical physics
(2011)
134,
114104
Ring-polymer instanton method for calculating tunneling splittings.
JO Richardson, SC Althorpe
– The Journal of Chemical Physics
(2011)
134,
054109
State-to-state reactive scattering in six dimensions using reactant-product decoupling: OH + H2 → H2O + H (J = 0)
MT Cvitaš, SC Althorpe
– Journal of Chemical Physics
(2011)
134,
024309
Symmetry Analysis of Geometric-Phase Effects in Quantum Dynamics
SC Althorpe
(2011)
17,
155
Differential cross sections for H + D 2 → HD( v ′ = 2, j ′ = 0,3,6,9) + D at center-of-mass collision energies of 1.25, 1.61, and 1.97 eV
NC-M Bartlett, J Jankunas, T Goswami, RN Zare, F Bouakline, SC Althorpe
– Phys. Chem. Chem. Phys.
(2010)
13,
8175
Chemistry. Setting the trap for reactive resonances.
SC Althorpe
– Science
(2010)
327,
1460
Strong geometric-phase effects in the hydrogen-exchange reaction at high collision energies: II. Quasiclassical trajectory analysis
F Bouakline, SC Althorpe, P Larregaray, L Bonnet
– Molecular Physics
(2010)
108,
969
Ring-polymer molecular dynamics rate-theory in the deep-tunneling regime: Connection with semiclassical instanton theory
JO Richardson, SC Althorpe
– J Chem Phys
(2009)
131,
214106
Influence of the geometric phase and non-adiabatic couplings on the dynamics of the H+H2 molecular system
F Bouakline, B Lepetit, SC Althorpe, A Kuppermann
– Springer Series in Chemical Physics
(2009)
97,
201
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Research Group

Research Interest Group

Telephone number

01223 336373

Email address

sca10@cam.ac.uk