Two-dimensional electronic spectra of an aggregating dye: simultaneous measurement of monomeric and dimeric line-shapes

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F09%3A00206896" target="_blank" >RIV/00216208:11320/09:00206896 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Two-dimensional electronic spectra of an aggregating dye: simultaneous measurement of monomeric and dimeric line-shapes

Popis výsledku v původním jazyce

We present a sequence of two-dimensional electronic spectra of a prototypical cyanine dye, whose spectral properties in aqueous solution are determined by the formation of a monomer-dimer equilibrium. Quantum-chemical methods are utilized to calculate the structure and absorption properties of the two species involved. Our spectroscopic results simultaneously characterize the spectral line-shapes of the two species in terms of underlying dynamic and static disorder, and demonstrate how the two-dimensional technique allows the exploitation of high spectral and temporal resolution in one and the same experiment. The distinctly different spectral relaxation dynamics are quantified in a two-dimensional line-shape analysis, by extracting the time dependentratios of the diagonal and anti-diagonal peak-widths. Our findings are in line with theoretical considerations, that predict the fluctuational dynamics of an excitonic dimer state to be exchange-narrowed by excitation delocalization.

Název v anglickém jazyce

Two-dimensional electronic spectra of an aggregating dye: simultaneous measurement of monomeric and dimeric line-shapes

Popis výsledku anglicky

We present a sequence of two-dimensional electronic spectra of a prototypical cyanine dye, whose spectral properties in aqueous solution are determined by the formation of a monomer-dimer equilibrium. Quantum-chemical methods are utilized to calculate the structure and absorption properties of the two species involved. Our spectroscopic results simultaneously characterize the spectral line-shapes of the two species in terms of underlying dynamic and static disorder, and demonstrate how the two-dimensional technique allows the exploitation of high spectral and temporal resolution in one and the same experiment. The distinctly different spectral relaxation dynamics are quantified in a two-dimensional line-shape analysis, by extracting the time dependentratios of the diagonal and anti-diagonal peak-widths. Our findings are in line with theoretical considerations, that predict the fluctuational dynamics of an excitonic dimer state to be exchange-narrowed by excitation delocalization.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

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Projekt

<a href="/cs/project/GP202%2F07%2FP278" target="_blank" >GP202/07/P278: Teorie multidimenzionální nelineární spektroskopie excitonových komplexů: Vztah mezi strukturou a funkcí fotosyntetických systémů</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2009

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Physical Chemistry Chemical Physics

ISSN

1463-9076

e-ISSN

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Svazek periodika

11

Číslo periodika v rámci svazku

28

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

12

Strana od-do

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Kód UT WoS článku

000268034900019

EID výsledku v databázi Scopus

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