Design and synthesis of new processible donor-acceptor dyad and triads

A. Dhanabalan; J. Knol; J.C. Hummelen; R.A.J. Janssen

doi:10.1016/S0379-6779(00)00912-7

Design and synthesis of new processible donor-acceptor dyad and triads

A. Dhanabalan
, J. Knol
, J.C. Hummelen
, R.A.J. Janssen

Materials to Optoelectronic Devices

Research output: Contribution to journal › Article › Academic › peer-review

24 Citations (Scopus)

Abstract

We report the design, synthesis and characterizarion of new processible well-defined donor (D)-acceptor (A) dyads and A-D-A triads for use in photovoltaic devices. The donor oligomers, which consist either of oligoaniline, thiophene-pyrrole-thiophene, phenyl-pyrrole-phenyl, or phenyl-thiophene-pyrrole-thiophene-phenyl segments, were covalently attached to fullerene C60 which acts an acceptor. All compounds were fully characterized using different analytical techniques.

Original language	English
Pages (from-to)	519-522
Journal	Synthetic Metals
Volume	119
Issue number	1-3
DOIs	https://doi.org/10.1016/S0379-6779(00)00912-7
Publication status	Published - 2001

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 7 Affordable and Clean Energy

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10.1016/S0379-6779(00)00912-7

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PY - 2001

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AB - We report the design, synthesis and characterizarion of new processible well-defined donor (D)-acceptor (A) dyads and A-D-A triads for use in photovoltaic devices. The donor oligomers, which consist either of oligoaniline, thiophene-pyrrole-thiophene, phenyl-pyrrole-phenyl, or phenyl-thiophene-pyrrole-thiophene-phenyl segments, were covalently attached to fullerene C60 which acts an acceptor. All compounds were fully characterized using different analytical techniques.

U2 - 10.1016/S0379-6779(00)00912-7

DO - 10.1016/S0379-6779(00)00912-7

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EP - 522

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JF - Synthetic Metals

IS - 1-3

ER -

Design and synthesis of new processible donor-acceptor dyad and triads

Abstract

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