By ultrafast spectroscopy the photophysics of water and propan-1-ol suspensions of different poly[N-9?-heptadecanyl-2,7-carbazole- alt -5,5-(4,7-di-2-thienyl-2?,1?,3?- benzothiadiazole] (PCDTBT) (nano)particles has been studied of different molar mass and size. High molar mass polymer (HMM > 20 kg/mol) forms nanoparticles with around 50 nm diameter via mini-emulsion post-polymerization, while low molar mass (LMM < 5 kg/mol) polymer prepared by dispersion polymerization results in particles with a diameter of almost one order of magnitude bigger (450 nm ±50 nm). In this study, the presence of excited-states and charge separated species was identified through UV pump and visible/near-infrared probe femtosecond transient absorption spectroscopy. A different behaviour for the HMM particles has been identified compared to the LMM ones. The HMM particles exhibit typical features of an energetically disordered conjugated polymer with a broad density of states, allowing for delayed spectral relaxation of excited states, while the LMM particles show a J-aggregate like behaviour where interchain interactions are less efficient. Stimulated emission in the red-near infrared region has been found in the LMM particles resulted to be a more energetically ordered system

Size-dependent photophysical behaviour of low bandgap semiconducting polymer particles

Tersilla Virgili;Chiara Botta;
2019

Abstract

By ultrafast spectroscopy the photophysics of water and propan-1-ol suspensions of different poly[N-9?-heptadecanyl-2,7-carbazole- alt -5,5-(4,7-di-2-thienyl-2?,1?,3?- benzothiadiazole] (PCDTBT) (nano)particles has been studied of different molar mass and size. High molar mass polymer (HMM > 20 kg/mol) forms nanoparticles with around 50 nm diameter via mini-emulsion post-polymerization, while low molar mass (LMM < 5 kg/mol) polymer prepared by dispersion polymerization results in particles with a diameter of almost one order of magnitude bigger (450 nm ±50 nm). In this study, the presence of excited-states and charge separated species was identified through UV pump and visible/near-infrared probe femtosecond transient absorption spectroscopy. A different behaviour for the HMM particles has been identified compared to the LMM ones. The HMM particles exhibit typical features of an energetically disordered conjugated polymer with a broad density of states, allowing for delayed spectral relaxation of excited states, while the LMM particles show a J-aggregate like behaviour where interchain interactions are less efficient. Stimulated emission in the red-near infrared region has been found in the LMM particles resulted to be a more energetically ordered system
2019
Istituto di fotonica e nanotecnologie - IFN
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
transient absorption spectroscopy
PCDTBT
Nanoparticles
Semiconducting polymer
Optoelecronics
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/367374
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