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Post Born-Oppenheimer Approximation for Semiclassical Spectroscopy Investigation of Proton-Coupled Electron Transfer Processes

Project description

Better molecular dynamics to decode quantum effects in molecular processes

Chemists have traditionally relied on the Born-Oppenheimer (BO) approximation, which simplifies molecular dynamics by treating electronic and nuclear motions separately. In addition, nuclear motion is usually simulated classically. However, this does not fully capture molecular complexity. For example, post-BO and nuclear quantum effects are key in proton-coupled electron transfer – a reaction that transfers at least an electron and a proton, which is crucial for photosynthesis and many biological processes. The NEOSC project, supported by the Marie Skłodowska-Curie Actions programme, combines the nuclear-electronic orbital approach (including protons in electronic calculations) with the semiclassical initial-value representation (to capture quantum effects for other nuclei). This framework will enable more accurate vibrational spectroscopy simulations and provide deeper insight into non-classical chemical processes.

Objective

The Born-Oppenheimer Approximation (BOA) has determined how chemists describe molecules since 1927. BOA separates electronic and nuclear degrees of freedom, considering that the electron timescale is much shorter than the nuclear one. This assumption does not hold in Proton Coupled Electron Transfer (PCET) processes. PCET is the key to efficiency in biological photosynthesis. Time-Resolved Infrared spectroscopy (TRIR) assists PCET investigations but it is usually interpreted with harmonic frequency calculations or classical nuclear dynamics simulations on a BO potential energy surface. To gain further physical insights into PCET it is necessary to revise the theoretical framework for spectroscopy, going beyond the BOA and including a quantum treatment for all nuclei. To reach this goal, this project unifies two cutting-edge methods. One is the Nuclear Electronic Orbital (NEO) approach that goes beyond the BOA by including into the electronic structure calculations the PCET transferred proton. The other is the Semiclassical Initial Value Representation technique that simulates IR spectra by accounting for quantum effects, such as the zero-point energy, overtones, or tunneling, for all nuclei, even in large molecular systems. The project will introduce a new post-BOA conceptual picture for vibrational spectroscopy. Specifically, semiclassical nuclear density calculations will be used to tailor new basis sets to efficiently simulate large molecular systems, gradually including many protons and other nuclei in the NEO wavefunction. In this way, a new spectroscopy theory will be developed for the simulation of TRIR spectra at semiclassical accuracy on NEO post-BOA PESs. These advances will be implemented in an open-source code that we employ to study prototypical PCET systems and gain accurate mechanistic information. This new knowledge will foster applied research by exploiting a deeper understanding of the PCET processes.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-TMA-MSCA-PF-GF - HORIZON TMA MSCA Postdoctoral Fellowships - Global Fellowships

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Call for proposal

(opens in new window) HORIZON-MSCA-2022-PF-01

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Coordinator

UNIVERSITA DEGLI STUDI DI MILANO
Net EU contribution
€ 288 859,20
Address
Via Festa Del Perdono 7
20122 Milano
Italy
Region
Nord-Ovest Lombardia Milano
Activity type
Higher or Secondary Education Establishments
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Total cost
No data

Partners (1)