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Nonadiabaticity in Biomolecular Vibrational Dynamics

Total Cost €


EC-Contrib. €






 NONABVD project word cloud

Explore the words cloud of the NONABVD project. It provides you a very rough idea of what is the project "NONABVD" about.

reverse    understating    structure    distinguished    inter    microscopic    proven    predictive    nanoscopic    description    confinement    electronic    relaxation    proteins    provides    excitation    concentration    foundation    anisotropy    environment    liquids    mechanisms    fluctuations    lifetimes    gradient    volumes    biological    dissipation    domain    mid    fundamental    molecular    phenomena    grant    interfaces    accounts    paradigm    micelles    theoretical    confined    scarce    investigation    vibrational    respiration    channel    dipolar    respective    membranes    erc    structural    diffusion    ir    cell    acceptor    solvation    nano    energy    starting    descriptions    biomolecular    interfacial    tremendous    transfers    vicinity    fluctuating    environments    dynamics    2018    underlying    elementary    thz    proton    ultrafast    translocation    modes    reactions    power    mobility    imposed    transport    concise    transmembrane    transfer    crowded    interactions    excess    region    nonadiabatic   

Project "NONABVD" data sheet

The following table provides information about the project.


Organization address
city: BERLIN
postcode: 12489

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 1˙486˙805 €
 EC max contribution 1˙486˙805 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31


Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FORSCHUNGSVERBUND BERLIN EV DE (BERLIN) coordinator 1˙486˙805.00


 Project objective

This ERC Starting Grant 2018 aims at the fundamental understanding of ultrafast biomolecular vibrational dynamics in the mid-IR/THz region and respective impact of nonadiabatic effects in dipolar liquids, within nano-confined environments and in the vicinity of biological interfaces. The understanding of these processes via underlying interactions is of fundamental importance with applications covering microscopic descriptions of elementary proton transfer reactions, mechanisms of energy dissipation upon vibrational excitation and solvation dynamics in biological relevant crowded environments. In particular knowledge on anisotropy of ultrafast vibrational energy relaxation together with information about distinguished intra- or inter-molecular acceptor modes, is scarce. As such the ERC Starting Grant 2018 transfers the paradigm of nonadiabatic relaxation, that has proven tremendous predictive power for descriptions of ultrafast electronic relaxation, to the low energy mid-IR/THz domain of biomolecular vibrational (energy relaxation) dynamics. As such the approach provides a description of microscopic phenomena like structural fluctuations, vibrational lifetimes and dissipation of excess energy. The proposed nonadiabatic approach to vibrational dynamics fully accounts for the strong impact of the fluctuating environment and will facilitate a concise theoretical descriptions of proton solvation structure, dynamics and transport within the confinement imposed by proton transport channel proteins. The investigation of proton mobility within reverse micelles will further facilitate the understating of proton structural diffusion within nanoscopic volumes. Such interfacial processes in the vicinity of biological membranes and proton translocation within transmembrane proteins are highly relevant as microscopic foundation of cell respiration driven by the gradient of proton concentration across membranes.

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The information about "NONABVD" are provided by the European Opendata Portal: CORDIS opendata.

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