Singlet fission in thin films of metallo-supramolecular polymers with ditopic thiophene-bridged terpyridine ligands

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F17%3A00477332" target="_blank" >RIV/61389013:_____/17:00477332 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11310/17:10368332

Výsledek na webu

<a href="http://dx.doi.org/10.1039/C7TC00484B" target="_blank" >http://dx.doi.org/10.1039/C7TC00484B</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/C7TC00484B" target="_blank" >10.1039/C7TC00484B</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Singlet fission in thin films of metallo-supramolecular polymers with ditopic thiophene-bridged terpyridine ligands

Popis výsledku v původním jazyce

The singlet fission (SF) phenomenon is currently investigated for its potential to overcome the Shockley–Queisser energy conversion efficiency limit of single-junction photovoltaic (PV) cells. One of the hurdles of using SF for PV cells is the limited choice among the presently available SF materials. We compare the photophysical behavior of thin solid films of two novel compounds: a ditopic ligand bis(terpyridine-4´-yl)terthiophene (T) and a metallo-supramolecular polymer (MSP), prepared by the coordination of T to Zn2+ ions (PT). The transient absorption kinetics in PT after photoexcitation into its second electronic excited state was consistent with an ultrafast (SF) process with a time constant of 160 fs. The lifetime of such a formed triplet state reached only 1 ns, due to mutual bimolecular annihilation, which also hindered the determination of the yield of the triplet state formation. In contrast, the metal-free thin films of T showed no signs of SF, but rather profound exciton relaxation through an excimer formation. Powder WAXS diffractograms pointed out a lower degree of structural order in the PT than that in the T – which may be the probable reason for differences in energy relaxation pathways of these two materials. To the best of our knowledge, singlet fission has not yet been reported in the MSP class of materials.

Název v anglickém jazyce

Singlet fission in thin films of metallo-supramolecular polymers with ditopic thiophene-bridged terpyridine ligands

Popis výsledku anglicky

The singlet fission (SF) phenomenon is currently investigated for its potential to overcome the Shockley–Queisser energy conversion efficiency limit of single-junction photovoltaic (PV) cells. One of the hurdles of using SF for PV cells is the limited choice among the presently available SF materials. We compare the photophysical behavior of thin solid films of two novel compounds: a ditopic ligand bis(terpyridine-4´-yl)terthiophene (T) and a metallo-supramolecular polymer (MSP), prepared by the coordination of T to Zn2+ ions (PT). The transient absorption kinetics in PT after photoexcitation into its second electronic excited state was consistent with an ultrafast (SF) process with a time constant of 160 fs. The lifetime of such a formed triplet state reached only 1 ns, due to mutual bimolecular annihilation, which also hindered the determination of the yield of the triplet state formation. In contrast, the metal-free thin films of T showed no signs of SF, but rather profound exciton relaxation through an excimer formation. Powder WAXS diffractograms pointed out a lower degree of structural order in the PT than that in the T – which may be the probable reason for differences in energy relaxation pathways of these two materials. To the best of our knowledge, singlet fission has not yet been reported in the MSP class of materials.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10404 - Polymer science

Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2017

Kód důvěrnosti údajů

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

Název periodika

Journal of Materials Chemistry C

ISSN

2050-7526

e-ISSN

—

Svazek periodika

5

Číslo periodika v rámci svazku

32

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

11

Strana od-do

8041-8051

Kód UT WoS článku

000407815800006

EID výsledku v databázi Scopus

2-s2.0-85027549097