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Ca/Alq3 hybrid cathode buffer layer for the optimization of organic solar cells based on a planar heterojunction

The Journal of physics and chemistry of solids, 2016-11, Vol.98, p.128-135

2016

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Linear Side Chains in Benzo[1,2‑b:4,5‑b′]dithiophene–Thieno[3,4‑c]pyrrole-4,6-dione Polymers Direct Self-Assembly and Solar Cell Performance

Journal of the American Chemical Society, 2013-03, Vol.135 (12), p.4656-4659

2013

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Smart geometrical approach to intercalate a highly absorbing and quite resistive electron donor layer in ternary organic photovoltaic cells

Organic electronics, 2020-01, Vol.76, p.105463, Article 105463

2020

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Ca/Alq sub(3) hybrid cathode buffer layer for the optimization of organic solar cells based on a planar heterojunction

The Journal of physics and chemistry of solids, 2016-11, Vol.98, p.128-135

2016

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Simply Complex: The Efficient Synthesis of an Intricate Molecular Acceptor for High-Performance Air-Processed and Air-Tested Fullerene-Free Organic Solar Cells

Chemistry of materials, 2017-02, Vol.29 (3), p.1309-1314

2017

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Synthesis of Molecular Dyads and Triads Based Upon N‐Annulated Perylene Diimide Monomers and Dimers

European journal of organic chemistry, 2018-12, Vol.2018 (48), p.6933-6943

2018

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Direct (Hetero)Arylation Polymerization of a Spirobifluorene and a Dithienyl-Diketopyrrolopyrrole Derivative: New Donor Polymers for Organic Solar Cells

Molecules (Basel, Switzerland), 2018-04, Vol.23 (4), p.962

2018

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Applying direct heteroarylation synthesis to evaluate organic dyes as the core component in PDI-based molecular materials for fullerene-free organic solar cells

Journal of materials chemistry. A, Materials for energy and sustainability, 2017, Vol.5 (23), p.11623-11633

2017

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Spectroscopic Engineering toward Near‐Infrared Absorption of Materials Containing Perylene Diimide

ChemPlusChem (Weinheim, Germany), 2017-11, Vol.82 (11), p.1359-1364

2017

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Ternary organic solar cells: using molecular donor or acceptor third components to increase open circuit voltage

New journal of chemistry, 2019-07, Vol.43 (26), p.1442-1448

2019

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The Optimization of Direct Heteroarylation and Sonogashira Cross-Coupling Reactions as Efficient and Sustainable Synthetic Methods To Access π‑Conjugated Materials with Near-Infrared Absorption

ACS sustainable chemistry & engineering, 2016-06, Vol.4 (6), p.3504-3517

2016

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Synthesis, characterization and use of benzothioxanthene imide based dimers

Chemical communications (Cambridge, England), 2020-09, Vol.56 (7), p.1131-1134

2020

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Effect of Length of Ethylene Glycol Sigma‐Linkers on Triphenylamine‐Based Dimers Used as Molecular Donors for Organic Solar Cells

ChemistrySelect (Weinheim), 2024-01, Vol.9 (2), p.n/a

2024

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Donor or Acceptor? How Selection of the Rylene Imide End Cap Impacts the Polarity of π‑Conjugated Molecules for Organic Electronics

ACS applied energy materials, 2018-09, Vol.1 (9), p.4906-4916

2018

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Effect of side chains on the electronic and photovoltaic properties of diketopyrrolopyrrole-based molecular acceptors

Organic electronics, 2016-10, Vol.37, p.479-484

2016

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Thienoisoindigo end-capped molecular donors for organic photovoltaics: Effect of the central π-conjugated connector

Dyes and pigments, 2017-10, Vol.145, p.7-11

2017

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Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications

Journal of materials chemistry. C, Materials for optical and electronic devices, 2018, Vol.6 (4), p.761-766

2018

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Thiochromenocarbazole imide: a new organic dye with first utility in large area flexible electroluminescent devices

Materials chemistry frontiers, 2022-07, Vol.6 (14), p.1912-1919

2022

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N-Annulation of the BTI Rylene Imide Organic Building Block: Impact on the Optoelectronic Properties of π-Extended Molecular Structures

Colorants, 2022-12, Vol.2 (1), p.22-30

2022

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Applying direct heteroarylation synthesis to evaluate organic dyes as the core component in PDI-based molecular materials for fullerene-free organic solar cellsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ta00318h

2017-06

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Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applicationsElectronic supplementary information (ESI) available. CCDC 1582576. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7tc05245f

2018-01

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1-Iodoacetylenes. 1. Spectroscopic evidence of their complexes with Lewis bases. A spectroscopic scale of soft basicity

Journal of the American Chemical Society, 1981-05, Vol.103 (10), p.2567-2573

1981

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1-Iodoacétylènes. IV. Relations structure-réactivité pour la complexation des 1-iodoacétylènes substitués avec des bases de Lewis

Canadian journal of chemistry, 1983-01, Vol.61 (1), p.135-138

1983

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Ca/Alq3 hybrid cathode buffer layer for the optimization of organic solar cells based on a planar heterojunction

Linear Side Chains in Benzo[1,2‑b:4,5‑b′]dithiophene–Thieno[3,4‑c]pyrrole-4,6-dione Polymers Direct Self-Assembly and Solar Cell Performance

Smart geometrical approach to intercalate a highly absorbing and quite resistive electron donor layer in ternary organic photovoltaic cells

Ca/Alq sub(3) hybrid cathode buffer layer for the optimization of organic solar cells based on a planar heterojunction

Simply Complex: The Efficient Synthesis of an Intricate Molecular Acceptor for High-Performance Air-Processed and Air-Tested Fullerene-Free Organic Solar Cells

Synthesis of Molecular Dyads and Triads Based Upon N‐Annulated Perylene Diimide Monomers and Dimers

Direct (Hetero)Arylation Polymerization of a Spirobifluorene and a Dithienyl-Diketopyrrolopyrrole Derivative: New Donor Polymers for Organic Solar Cells

Applying direct heteroarylation synthesis to evaluate organic dyes as the core component in PDI-based molecular materials for fullerene-free organic solar cells

Spectroscopic Engineering toward Near‐Infrared Absorption of Materials Containing Perylene Diimide

Ternary organic solar cells: using molecular donor or acceptor third components to increase open circuit voltage

The Optimization of Direct Heteroarylation and Sonogashira Cross-Coupling Reactions as Efficient and Sustainable Synthetic Methods To Access π‑Conjugated Materials with Near-Infrared Absorption

Synthesis, characterization and use of benzothioxanthene imide based dimers

Effect of Length of Ethylene Glycol Sigma‐Linkers on Triphenylamine‐Based Dimers Used as Molecular Donors for Organic Solar Cells

Donor or Acceptor? How Selection of the Rylene Imide End Cap Impacts the Polarity of π‑Conjugated Molecules for Organic Electronics

Effect of side chains on the electronic and photovoltaic properties of diketopyrrolopyrrole-based molecular acceptors

Thienoisoindigo end-capped molecular donors for organic photovoltaics: Effect of the central π-conjugated connector

Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications

Thiochromenocarbazole imide: a new organic dye with first utility in large area flexible electroluminescent devices

N-Annulation of the BTI Rylene Imide Organic Building Block: Impact on the Optoelectronic Properties of π-Extended Molecular Structures

Applying direct heteroarylation synthesis to evaluate organic dyes as the core component in PDI-based molecular materials for fullerene-free organic solar cellsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ta00318h

Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applicationsElectronic supplementary information (ESI) available. CCDC 1582576. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7tc05245f

1-Iodoacetylenes. 1. Spectroscopic evidence of their complexes with Lewis bases. A spectroscopic scale of soft basicity

1-Iodoacétylènes. IV. Relations structure-réactivité pour la complexation des 1-iodoacétylènes substitués avec des bases de Lewis

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