Diels-Alders adducts of C60 and esters of 3-(1-indenyl)-propionic acid: alternatives for [60]PCBM in polymer:fullerene solar cells

Alex  Sieval; Neil D Treat; Desirée Rozema; Jan C Hummelen; Natalie Stingelin

doi:10.1039/c5cc01642h

Diels-Alders adducts of C60 and esters of 3-(1-indenyl)-propionic acid: alternatives for [60]PCBM in polymer:fullerene solar cells

Alex Sieval, Neil D Treat, Desirée Rozema, Jan C Hummelen, Natalie Stingelin

Solenne BV

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

Abstract

A series of new, easily synthesized C60-fullerene derivatives is introduced that allow for optimization of the interactions between rr-P3HT and the fullerene by systematic variation of the size of the ester group. Two compounds gave overall cell efficiencies of 4.8%, clearly outperforming [60]PCBM which gives 4.3% under identical conditions.

Original language	English
Pages (from-to)	8126-8129
Number of pages	4
Journal	Chemical Communications
Volume	51
Issue number	38
DOIs	https://doi.org/10.1039/c5cc01642h
Publication status	Published - 11 May 2015

UN SDGs

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

SDG 12 Responsible Consumption and Production

Keywords

derivatives
esters
organic solar cells

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10.1039/c5cc01642h

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abstract = "A series of new, easily synthesized C60-fullerene derivatives is introduced that allow for optimization of the interactions between rr-P3HT and the fullerene by systematic variation of the size of the ester group. Two compounds gave overall cell efficiencies of 4.8\%, clearly outperforming [60]PCBM which gives 4.3\% under identical conditions. ",

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language = "English",

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AU - Rozema, Desirée

AU - Hummelen, Jan C

AU - Stingelin, Natalie

PY - 2015/5/11

Y1 - 2015/5/11

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AB - A series of new, easily synthesized C60-fullerene derivatives is introduced that allow for optimization of the interactions between rr-P3HT and the fullerene by systematic variation of the size of the ester group. Two compounds gave overall cell efficiencies of 4.8%, clearly outperforming [60]PCBM which gives 4.3% under identical conditions.

KW - derivatives

KW - esters

KW - organic solar cells

KW - derivaten

KW - esters

KW - organische zonnecellen

U2 - 10.1039/c5cc01642h

DO - 10.1039/c5cc01642h

M3 - Article

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SN - 1359-7345

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JO - Chemical Communications

JF - Chemical Communications

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ER -

Diels-Alders adducts of C60 and esters of 3-(1-indenyl)-propionic acid: alternatives for [60]PCBM in polymer:fullerene solar cells

Abstract

UN SDGs

Keywords

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